WO2016163465A1 - Disease analysis apparatus, disease risk analysis system, and disease analysis program - Google Patents

Disease analysis apparatus, disease risk analysis system, and disease analysis program Download PDF

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Publication number
WO2016163465A1
WO2016163465A1 PCT/JP2016/061419 JP2016061419W WO2016163465A1 WO 2016163465 A1 WO2016163465 A1 WO 2016163465A1 JP 2016061419 W JP2016061419 W JP 2016061419W WO 2016163465 A1 WO2016163465 A1 WO 2016163465A1
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Prior art keywords
blood pressure
disease
pressure data
information
blood
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PCT/JP2016/061419
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French (fr)
Japanese (ja)
Inventor
稗田 克彦
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Jsr株式会社
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/022Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers

Definitions

  • the present disclosure relates to a disease analysis device, a disease risk analysis system, and a disease analysis program recording medium, for example, a disease analysis device, a disease risk analysis system, and a disease analysis program recording medium based on blood pressure information and the like.
  • Patent Document 1 it is possible to suppress a decrease in analysis accuracy or prediction accuracy due to a difference in blood pressure value among individuals, a difference in blood pressure value due to season, or the like.
  • a difference in blood pressure value due to season or the like.
  • There is a limit in eliminating the influence due to the difference in blood pressure value, etc. and there is a problem that it is difficult to further improve analysis accuracy or prediction accuracy.
  • the disease analysis apparatus includes a blood vessel related data storage unit that stores blood vessel related data of a subject continuously measured in a blood vessel related data measurement unit, and a blood pressure based on the blood vessel related data.
  • a blood pressure data calculation unit for calculating data, a blood pressure data storage unit for storing the blood pressure data calculated in the blood pressure data calculation unit, and at least two arbitrary blood pressure data stored in the blood pressure data storage unit Refers to a blood pressure change information calculation unit that acquires blood pressure data, calculates change information that is information relating to the amount of change of the acquired at least two blood pressure data, and a blood pressure disease database in which the change information and disease risk information are associated And acquiring the disease risk information associated with the change information calculated by the blood pressure change information calculation unit.
  • the disease risk analysis system is information related to a biological information acquisition device including a blood vessel-related data measurement unit that measures blood vessel-related data of a subject, and changes in at least two blood pressure data.
  • Blood vessel related data for storing the blood vessel related data of the subject continuously measured in the blood vessel related data measuring unit, and a disease information management device having a blood pressure disease database in which change information and disease risk information are associated
  • a blood pressure data calculation unit that calculates the blood pressure data based on the blood vessel related data, the blood pressure data storage unit calculated in the blood pressure data calculation unit, and the blood pressure stored in the blood pressure data storage unit Any at least two blood pressure data are acquired from the data, and the change relating to the acquired at least two blood pressure data is performed.
  • a disease analysis comprising: a blood pressure change information calculation unit that calculates information; and a disease analysis unit that references the blood pressure disease database and acquires the disease risk information associated with the change information and analyzes the disease risk And a device.
  • a disease analysis program stored in a non-transitory computer-readable medium is a computer that stores blood pressure data based on at least two blood vessel-related data measured at different times in a blood vessel-related data measurement unit.
  • the blood pressure disease database in which the change information and the disease risk information are associated with each other, and the blood pressure change information calculation function for calculating change information that is information relating to the amount of change in the acquired at least two blood pressure data.
  • a disease analysis function for obtaining the disease risk information associated with the change information and analyzing the disease risk.
  • the disease risk analysis system according to the second aspect, and the disease analysis program according to the third aspect, information on the amount of change in any at least two blood pressure data (
  • the disease risk is also analyzed based on the disease risk information associated with the change information. Therefore, compared with the case of analyzing the disease risk based on the absolute value of the blood pressure data, it becomes easier to perform an analysis in which the influence due to the difference in blood pressure value among individuals, the difference in blood pressure value depending on the season, and the like is eliminated.
  • an association between the disease risk and the change information an association based on statistical processing can be exemplified.
  • the disease risk analysis system according to the second aspect of the present disclosure, the disease risk analysis system according to the second aspect, and the disease analysis program according to the third aspect, change information and the disease risk associated with the change information Based on this information, disease risk analysis is performed. Therefore, compared to the case of analyzing the disease risk based on the absolute value of the blood pressure data, there is an effect that it is easy to improve the analysis accuracy of the disease.
  • the disease risk analysis system 1 is a system that analyzes a disease risk of a subject 50 based on blood pressure data calculated based on pulse wave data of the subject 50 that is continuously measured.
  • the device 30 is included in the disease risk analysis system 1.
  • the disease risk analysis system 1 is mainly provided with a blood vessel monitor (biological information acquisition device) 10 based on pulse wave data, a disease information management device 20, and a disease analysis device 30. It has been.
  • continuous measurement is a concept that includes both measurement without interruption and measurement at regular intervals.
  • the measurement is performed every few hours from one measurement of each pulse, and is a blood vessel monitor. From the viewpoint of reducing the power consumption of 10, it is preferable to measure at regular intervals of several minutes to several hours.
  • the blood vessel monitor 10 is attached to the subject 50, and continuously measures the blood pressure of the subject 50.
  • the blood vessel monitor 10 is provided with at least a blood vessel pulse wave sensor (blood vessel related data measuring unit) 11, a time measuring unit 12, and a monitor side input / output unit 13.
  • the blood vessel pulse wave sensor 11 continuously measures the blood vessel pulse wave of the subject 50 and outputs blood vessel pulse wave data (blood vessel related data) that is data relating to the value of the measured blood vessel pulse wave.
  • Reference numeral 12 denotes time information that is time information at the time when the blood vessel pulse wave data is measured.
  • the monitor-side input / output unit 13 outputs vascular pulse wave data and time information to the disease analyzer 30.
  • the vascular pulse wave sensor 11 is applied to a sensor that irradiates the subject 50 with light such as near infrared rays and continuously measures the vascular pulse wave based on a phase change in the reflected or transmitted light.
  • the blood vessel pulse wave sensor 11 is not limited to a sensor based on the above-described method, and may be a sensor based on another method that can be continuously measured, and the measurement method is not limited.
  • the vascular pulse wave is a physical property value related to the blood vessel measured by the vascular pulse wave sensor 11, and refers to a value that repeatedly changes with the pulsation of the heart, such as the volume of the blood vessel.
  • the blood pressure can be used.
  • the monitor-side input / output unit 13 is a communication unit that transmits and receives information to and from the disease analysis device 30.
  • Communication with the disease analyzer 30 may be wired communication or wireless communication, or may be a combination of both.
  • description will be made by applying to an example in which communication with the disease analysis apparatus 30 is performed using a short-range wireless communication technology with low power consumption such as Bluetooth (registered trademark).
  • Bluetooth registered trademark
  • the communication method is not limited to this, and other wireless communication technologies such as Wi-Fi may be used.
  • the disease information management apparatus 20 is a computer system having a CPU (Central Processing Unit), ROM, RAM, hard disk, input / output interface and the like. In the present embodiment, description will be made by applying to an example of a database server connected to the disease analysis device 30 so as to be capable of information communication.
  • CPU Central Processing Unit
  • ROM Read Only Memory
  • RAM Random Access Memory
  • hard disk hard disk
  • input / output interface and the like.
  • description will be made by applying to an example of a database server connected to the disease analysis device 30 so as to be capable of information communication.
  • the control program stored in the ROM or the like causes the hard disk or the like to function as the blood pressure disease database 21 and causes the input / output interface or the like to function as the management-side input / output unit 22. It functions as a control unit that controls the operation of the management-side input / output unit 22.
  • the blood pressure disease database 21 stores at least differential information and disease risk information, which will be described later, in a statistically correlated manner.
  • the stored disease risk information can be output from the blood pressure disease database 21 to the disease analysis device 30 via the management input / output unit 22.
  • the statistically related difference information and disease risk information are the results of associating the difference information accumulated so far and the disease risk information by performing statistical processing, and are stored in the blood pressure disease database 21 in advance. What is stored can be exemplified. Note that the statistical association between the difference information and the disease risk information may be periodically updated.
  • the management-side input / output unit 22 is a communication unit that transmits and receives information to and from the disease analysis device 30.
  • Communication with the disease analyzer 30 may be wired communication or wireless communication, or may be a combination of both.
  • a radio base station is disposed between the disease information management apparatus 20 and the disease analysis apparatus 30, and between the disease information management apparatus 20 and the radio base station, the Internet, an intranet, a LAN (local area network), or the like. Network), etc., and is applied to an example in which communication between the wireless base station and the disease analyzer 30 is performed using wireless communication technology such as Wi-Fi (registered trademark). explain.
  • the disease analyzer 30 can include a display unit.
  • the display unit is a device that displays blood vessel pulse wave data transmitted from the blood vessel monitor 10 or a calculation result of the disease analysis device 30.
  • the calculation result of the disease analyzer 30 specifically, the calculation results of the blood pressure data calculation unit 36 and the disease analysis unit 32 described later can be displayed, and blood pressure, pulse, blood flow velocity, blood flow rate, pulse rate, It is possible to display biological information such as blood glucose level and information on disease risk.
  • a display unit an appropriate display or the like can be used.
  • the disease analyzer 30 is a computer system having a CPU (Central Processing Unit), ROM, RAM, hard disk, input / output interface, and the like.
  • CPU Central Processing Unit
  • ROM Read Only Memory
  • RAM Random Access Memory
  • hard disk hard disk
  • input / output interface and the like.
  • description will be made by applying to an example in which the disease analysis device 30 is a portable terminal owned by a portable subject 50, such as a portable information terminal device (smart phone or tablet PC).
  • a control program stored in a non-volatile memory causes the CPU to function at least as the blood pressure change information calculation unit 31, the blood pressure data calculation unit 36, and the disease analysis unit 32.
  • the input / output interface or the like functions as the analysis-side input / output unit 34, and the nonvolatile memory or the like functions as the blood vessel pulse wave data storage unit 37 and blood pressure data storage unit 33.
  • the blood vessel pulse wave data storage unit 37 stores the blood vessel pulse wave data continuously measured by the blood vessel monitor 10 and time information at the time when the blood vessel pulse wave data is measured in association with each other.
  • the vascular pulse wave data storage unit 37 can store the vascular pulse wave data and time information input from the blood vessel monitor 10 and can output the stored vascular pulse wave data to the blood pressure data calculation unit 36. ing.
  • the blood pressure data storage unit 33 stores the blood pressure data calculated by the blood pressure data calculation unit 36 and time information at the time when the blood vessel pulse wave data corresponding to the blood pressure data is measured in association with each other.
  • the blood pressure data storage unit 33 can store the blood pressure data and time information input from the blood pressure data calculation unit 36 and can output the stored blood pressure data to the blood pressure change information calculation unit 31.
  • the blood pressure data calculation unit 36 calculates blood pressure data from the blood vessel pulse wave data stored in the blood vessel pulse wave data storage unit 37.
  • a known calculation method can be used, and it is not particularly limited.
  • the blood pressure change information calculation unit 31 acquires at least two blood pressure data from the blood pressure data stored in the blood pressure data storage unit 33, and calculates difference information as change information of the acquired at least two blood pressure data.
  • the acquired blood pressure data is selected from a plurality of blood pressure data linked to predetermined time information.
  • the difference information is calculated as an example of the change information of the two blood pressure data.
  • the change information only needs to be information that indicates the change of the two blood pressure data. It is not limited.
  • the disease analysis unit 32 refers to the blood pressure disease database 21, acquires disease risk information associated with the difference information, and analyzes the disease risk.
  • a known method can be used, and it is not particularly limited.
  • the analysis-side input / output unit 34 is a communication unit that transmits and receives information to and from the monitor-side input / output unit 13 and the management-side input / output unit 22 as described above.
  • the analysis side input / output unit 34 is applied to an example in which a part that communicates with the monitor side input / output unit 13 and a part that communicates with the management side input / output unit 22 are provided. I will explain.
  • the blood vessel pulse wave sensor 11 When the blood vessel monitor 10 is attached to the subject 50, the blood vessel pulse wave sensor 11 starts to continuously measure the blood vessel pulse wave of the subject 50 (measurement step: S11).
  • the vascular pulse wave sensor 11 outputs vascular pulse wave data which is an output corresponding to the measured vascular pulse wave.
  • the blood vessel pulse wave data is transmitted from the monitor-side input / output unit 13 to the disease analysis device 30 together with time information indicating the time output from the time measurement unit 12 (transmission step: S12).
  • the analysis-side input / output unit 34 receives the blood vessel pulse wave data transmitted from the blood vessel monitor 10 and time information corresponding thereto (reception step: S13).
  • the received vascular pulse wave data is linked to the time information corresponding thereto and stored in the vascular pulse wave data storage unit 37 (vascular pulse wave data storage step: S14).
  • the vascular pulse wave data and the time information to the vascular pulse wave data storage unit 37 may be stored every time the vascular pulse wave of the subject 50 is measured by the vascular monitor 10, or the vascular pulse wave is measured. It may be stored at a timing different from the timing.
  • blood vessel pulse wave data or the like is stored in a temporary storage unit such as a memory provided in the blood vessel monitor 10 or the disease analysis device 30, and the blood vessel is transferred from the temporary storage unit at the timing of storage.
  • the blood vessel pulse wave data and time information may be stored in the pulse wave data storage unit 37.
  • the blood pressure data calculation unit 36 of the disease analysis apparatus 30 performs a process of calculating blood pressure data from the blood vessel pulse wave data stored in the blood vessel pulse wave data storage unit 37 (blood pressure data calculation step: S15). Specifically, processing for calling blood vessel pulse wave data for which blood pressure data is not calculated from the blood vessel pulse wave data storage unit 37 and processing for calculating blood pressure data based on the called blood vessel pulse wave data are performed. It should be noted that the value of the sphygmomanometer is corrected by using the blood pressure data measured by the cuff type electronic sphygmomanometer used conventionally or the value of the blood pressure data measured by the catheter type blood pressure measuring method. May be.
  • the calculated blood pressure data is linked to the time information corresponding to the calculated blood pressure data and stored in the blood pressure data storage unit 33 (blood pressure data storage step: S16).
  • the blood pressure data calculation and storage process may be performed continuously following the blood vessel pulse wave data storage process as described above, or a predetermined unique timing separately from the blood vessel pulse wave data storage process. There is no particular limitation.
  • the disease risk analysis may be automatically performed according to a predetermined schedule, or may be performed based on an instruction to start analysis input from the outside, and is not particularly limited in timing for starting the analysis. Absent.
  • the disease analysis unit 32 of the disease analysis device 30 executes a process of acquiring at least two blood pressure data measured at different times (blood pressure data acquisition step: S21).
  • the latest blood pressure data for example, blood pressure data measured at a desired timing one hour before one beat
  • blood pressure data measured at the same time on the previous day hereinafter “past blood pressure data”. This is also applied to an example of acquiring.
  • blood pressure data measured within the same day such as several minutes ago and several hours ago. It may be used and is not particularly limited. By using the past blood pressure data several minutes ago and several hours ago, it becomes easier to grasp in detail blood pressure fluctuations in the subject 50 such as early morning, morning, afternoon, evening, nighttime, sleeping, etc. It is possible to easily improve the accuracy of disease analysis.
  • blood pressure data measured at a timing further back in the past such as the same time on the predetermined day of the previous week, the previous month, or the previous year, may be used, and is not particularly limited. By making it possible to use past blood pressure data such as the previous week, the previous month, and the previous year, it becomes easy to grasp the state change of the subject 50 from the past, and it is possible to easily improve the analysis accuracy of the disease.
  • the latest blood pressure data and the past blood pressure data may be average blood pressure data obtained based on a plurality of blood pressure data.
  • the average value of several blood pressure data measured at desired multiple timings one hour before one beat, or several pieces measured at the same time in the period from several days up to the previous day It may be an average value of blood pressure data.
  • the blood pressure change information calculation unit 31 performs a process of calculating difference information, which is a difference value between the acquired two blood pressure data, as change information regarding the change amount of the two blood pressure data (blood pressure change information calculation step: S22). .
  • the calculated difference information is output from the analysis side input / output unit 34 to the management side input / output unit 22 of the disease information management apparatus 20.
  • the disease information management device 20 performs a process of selecting disease risk information stored in the blood pressure disease database 21 and associated with the difference information having the same value as the input difference information (disease) Risk information selection step: S23).
  • the selected disease risk information is output from the management-side input / output unit 22 to the analysis-side input / output unit 34 of the disease analyzer 30.
  • the disease analysis unit 32 of the disease analysis device 30 performs a calculation process for analyzing the disease risk of the subject 50 based on the acquired disease risk information (disease analysis step: S24).
  • the disease risk obtained by the analysis is output from the disease analyzer 30 to the outside.
  • the output destination may be, for example, a display device such as a display that conveys a disease risk to the subject 50, or an information processing device such as a server installed in a medical institution where the subject 50 visits. Also good.
  • the disease risk analysis system 1 and the disease analysis device 30 configured as described above, the disease risk based on the difference information of any at least two blood pressure data and the disease risk information statistically associated with the difference information. Analysis is performed. Therefore, compared with the case of analyzing the disease risk based on the absolute value of blood pressure data, it becomes easier to perform an analysis that excludes the effects of differences in blood pressure values by 50 subjects, blood pressure values by season, etc. It is possible to easily improve the accuracy of disease analysis.
  • early morning hypertension is known to be related to stroke risk, and it is easier to improve the accuracy of disease analysis by analyzing stroke risk based on blood pressure fluctuations and daily differences in the early morning.
  • daytime stress hypertension is related to heart disease and stroke risk, and by analyzing the risk of heart disease and stroke based on fluctuations in blood pressure during the day and daily differences, It is possible to easily improve the accuracy of disease analysis.
  • nighttime hypertension is related to diabetes risk, and it is easier to improve the accuracy of disease analysis by analyzing diabetes risk based on fluctuations in blood pressure during nighttime and daily differences. Can do.
  • the difference information related to the time information can be obtained by associating and storing the time information with the blood pressure data. For example, blood pressure data acquired based on time information can be selected, and difference information can be obtained based on the selected blood pressure data. Time information used for selection can be arbitrarily set, and change information related to desired time information can be obtained.
  • the average blood pressure data obtained based on a plurality of blood pressure data as the latest blood pressure data and the past blood pressure data, the influence of variations caused by the external environment etc. included in each blood pressure data Can be suppressed, and the analysis accuracy of the disease can be easily improved.
  • the disease information management apparatus 20 in the above-described embodiment is provided with a personal information database 23 in which a management ID related to the subject 50, a password, and attribute data related to disease analysis information are stored. May be.
  • the disease risk associated with the subject 50 from the blood pressure disease database 21 by using the attribute data stored in the personal information database 23 in the calculation process for analyzing the disease risk of the subject 50 in S24. Information can be used. As a result, compared with the case where attribute data is not used, it is possible to easily improve the accuracy of disease analysis.
  • the blood vessel monitor 10 detects whether or not the blood vessel monitor 10 is attached to the subject 50, and outputs an ON signal when the blood vessel monitor 10 is attached to the subject 50, and when the blood vessel monitor 10 is detached from the subject 50. May be provided with a sensor that outputs an OFF signal. By transmitting such an ON / OFF signal to the disease analyzer 30, it is possible to prevent blood pressure data transmitted when the blood vessel monitor 10 is removed from the subject 50 from being used for disease risk analysis.
  • the blood vessel monitor 10 is described as applied to an example in which the blood vessel pulse wave is measured and the blood vessel pulse wave data is output.
  • values such as a pulse including blood pressure and blood flow can be calculated. What is necessary is just to measure various physical property values and output the data, and does not limit the measurement object.
  • a second embodiment of the present disclosure will be described with reference to FIG.
  • the basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configurations of the blood vessel monitor and the disease analysis device are different from those of the first embodiment. Therefore, in the present embodiment, only the periphery of the blood vessel monitor and the disease analysis apparatus will be described using FIG. 5, and description of other components will not be repeated.
  • the disease risk analysis system 101 of the present embodiment is mainly provided with a blood vessel monitor (biological information acquisition device) 110, a disease information management device 20, and a disease analysis device 130. .
  • the blood vessel monitor 110 is attached to the subject 50.
  • the blood vessel monitor 110 is provided with at least a blood vessel pulse wave sensor 11, a time measurement unit 12, a monitor side input / output unit 13, and a temperature measurement unit (temperature measurement unit) 114.
  • the temperature measuring unit 114 is a sensor that measures the temperature of the subject 50 to which the blood vessel monitor 110 is attached, for example, the temperature of the body surface.
  • the measured temperature of the body surface of the subject 50 is transmitted from the temperature measurement unit 114 to the disease analysis device 130 via the monitor side input / output unit 13 as temperature information related to the temperature.
  • the position where the blood vessel monitor 110 is attached in this embodiment is exemplified by a position close to the heart of the subject 50.
  • the place where the blood vessel monitor 110 is attached is desirably a body surface corresponding to the chest coronary artery.
  • the disease analyzer 130 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 130 is a portable information terminal device owned by a portable subject 50.
  • a control program stored in a non-volatile memory uses a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and an activity status determination unit (determination).
  • Part) 135 at least functions as an input / output interface 34 as an analysis-side input / output part 34 and functions as a vascular pulse wave data storage part 37 and a blood pressure data storage part 33. Is.
  • the activity status determination unit 135 determines the activity status of the subject 50 based on the temperature information on the body surface input from the temperature measurement unit 114 of the blood vessel monitor 110, and outputs the activity status information that is the determination result. To do.
  • the activity state information is stored in the blood pressure data storage unit 33 in association with blood pressure data measured at the same time as the temperature information measurement.
  • the activity status of the subject 50 based on the temperature information in the activity status determination unit 135 will be described.
  • a human body temperature fluctuates according to the activity state.
  • the activity status can be determined based on the value of the body temperature and the fluctuation. For example, it is known that a human body temperature rapidly decreases after falling asleep and then increases when the user awakes. By utilizing this temperature change, it is possible to estimate whether or not the subject 50 is in a sleep state.
  • the control of the disease risk analysis in the disease analyzer 130 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
  • the associated activity state information is also referred to when acquiring blood pressure data.
  • a process of acquiring blood pressure data used for calculation of change information from a plurality of blood pressure data associated with the same activity state information such as a sleep state is performed.
  • the disease risk analysis is performed based also on the activity state information of the subject 50, so that it is possible to easily improve the analysis accuracy of the disease. That is, in the case of disease risk analysis using both blood pressure data acquired in a state where the acquired blood pressure data is significantly different, such as a sleep state and a wakefulness state, the analysis accuracy is likely to decrease. As described above, based on the activity state information, for example, the case of disease risk analysis using only blood pressure data acquired in the sleep state is possible, and it becomes easy to improve the analysis accuracy of the disease. [Third Embodiment] Next, a third embodiment of the present disclosure will be described with reference to FIG.
  • the basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configurations of the blood vessel monitor and the disease analysis device are different from those of the first embodiment. Therefore, in the present embodiment, only the periphery of the blood vessel monitor and the disease analysis apparatus will be described using FIG. 6, and description of other components will not be repeated.
  • the disease risk analysis system 201 of the present embodiment is mainly provided with a blood vessel monitor (biological information acquisition device) 210, a disease information management device 20, and a disease analysis device 230. .
  • the blood vessel monitor 110 is attached to the subject 50.
  • the blood vessel monitor 110 is provided with at least a blood vessel pulse wave sensor 11, a time measurement unit 12, a monitor-side input / output unit 13, and an acceleration measurement unit (acceleration measurement unit) 214.
  • the acceleration measuring unit 214 is a triaxial acceleration sensor that measures the movement of the body of the subject 50 to which the blood vessel monitor 210 is attached as acceleration.
  • the measured acceleration of the subject 50 is transmitted from the acceleration measuring unit 214 to the disease analyzer 230 via the monitor side input / output unit 13 as acceleration information related to the acceleration.
  • the disease analyzer 230 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 230 is a portable information terminal device owned by a portable subject 50.
  • a control program stored in a non-volatile memory uses a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and an activity status determination unit (determination).
  • Part) 235 to function as at least, input / output interface or the like to function as analysis side input / output part 34, and non-volatile memory to function as vascular pulse wave data storage part 37 and blood pressure data storage part 33 It is.
  • the activity status determination unit 235 determines the activity status of the subject 50 based on the body acceleration information input from the acceleration measurement unit 214 of the blood vessel monitor 210, and outputs the activity status information as the determination result. Is.
  • the activity state information is stored in the blood pressure data storage unit 33 in association with blood pressure data measured at the same time as the measurement of acceleration information.
  • the determination of the activity status of the subject 50 based on the acceleration information in the activity status determination unit 235 will be described.
  • humans move their bodies according to their activity status, in other words, the value of acceleration varies.
  • the activity status can be determined based on the acceleration value and the fluctuation. For example, it is known that human beings generally stop moving in a sleep state. Therefore, it is possible to estimate whether or not the subject 50 is in a sleep state based on whether or not the vibration width of the acceleration value falls within the predetermined amplitude range.
  • the movement state of the subject 50 such as walking and running, and the local movement state such as moving the neck, moving the arm, moving the foot, etc. It becomes.
  • the subject 50 is moving while using a moving device such as a train, an elevator, or a vehicle, or walking, It is possible to determine whether the vehicle is running, desk work, or sleeping.
  • the control of the disease risk analysis in the disease analyzer 230 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
  • the associated activity state information is also referred to when acquiring blood pressure data.
  • a process of acquiring blood pressure data used for calculation of change information from a plurality of blood pressure data associated with the same activity state information such as a sleep state is performed.
  • the activity state of the subject 50 can be determined more finely than in the first embodiment and the second embodiment described above. Therefore, it becomes easier to improve the analysis accuracy of the disease.
  • a fourth embodiment of the present disclosure will be described with reference to FIG.
  • the basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in this embodiment, only the periphery of the disease analyzer will be described with reference to FIG. 7, and description of other components and the like will not be repeated.
  • the disease risk analysis system 301 of the present embodiment is mainly provided with a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 330.
  • the disease analyzer 330 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 330 is a portable information terminal device owned by a portable subject 50.
  • a control program stored in a non-volatile memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a physical information input unit 335. At least it is made to function, and an input / output interface or the like is made to function as the analysis side input / output unit 34, and a nonvolatile memory or the like is made to function as the blood vessel pulse wave data storage unit 37 and the blood pressure data storage unit 33.
  • the body information input unit 335 is used to input body information such as the gender, height, weight, and body fat percentage of the subject 50.
  • the input physical information is stored in, for example, the hard disk of the disease analysis device 330, and is read out and used for analysis in the disease risk analysis in the disease analysis unit 32.
  • the disease risk analysis can be performed in consideration of the body information of the subject 50 as compared with the first embodiment described above, and thus the disease analysis It becomes easier to improve accuracy.
  • a fifth embodiment of the present disclosure will be described with reference to FIG.
  • the basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in this embodiment, only the periphery of the disease analyzer will be described using FIG. 8, and description of other components and the like will not be repeated.
  • a blood vessel monitor 10 In the disease risk analysis system 401 of this embodiment, as shown in FIG. 8, a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 430 are mainly provided.
  • the disease analyzer 430 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 430 is a portable information terminal device owned by a portable subject 50.
  • a control program stored in a non-volatile memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a life information input unit 435. At least it is made to function, and an input / output interface or the like is made to function as the analysis side input / output unit 34, and a nonvolatile memory or the like is made to function as the blood vessel pulse wave data storage unit 37 and the blood pressure data storage unit 33.
  • the life information input unit 435 is used to input life information such as the eating habits of the subject 50, sleeping hours, and smoking habits.
  • the input life information is stored in, for example, the hard disk of the disease analysis device 430, and is read out and used for analysis in the disease risk analysis in the disease analysis unit 32.
  • the disease risk analysis can be performed in consideration of the life information of the subject 50 as compared with the first embodiment and the like. It becomes easier to improve accuracy.
  • a sixth embodiment of the present disclosure will be described with reference to FIG.
  • the basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in the present embodiment, only the periphery of the disease analyzer will be described using FIG. 9, and description of other components and the like will not be repeated.
  • the disease risk analysis system 501 of the present embodiment mainly includes a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 530.
  • the disease analyzer 530 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like.
  • the disease analysis apparatus 530 will be described as applied to an example of a portable information terminal apparatus owned by a portable subject 50.
  • a control program stored in a non-volatile memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a pulse data calculation unit 535. At least it is made to function, and an input / output interface or the like is made to function as the analysis side input / output unit 34, and a nonvolatile memory or the like is made to function as the blood vessel pulse wave data storage unit 37 and the blood pressure data storage unit 33.
  • the pulse data calculation unit 535 calculates pulse data of the subject 50 based on the blood vessel pulse wave data.
  • the vascular pulse wave data stored in the vascular pulse wave data storage unit 37 is called, and the pulse data is calculated based on the called vascular pulse wave data.
  • a known method can be used and is not particularly limited.
  • the calculated pulse data is associated with blood pressure data calculated from the same vascular pulse wave data and stored in the blood pressure data storage unit 33.
  • the control of the disease risk analysis in the disease analyzer 530 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
  • linked pulse data when acquiring blood pressure data, linked pulse data is also referred to.
  • disease risk analysis can be performed in consideration of the pulse data of the subject 50 as compared with the first embodiment described above. It becomes easier to improve accuracy.
  • a seventh embodiment of the present disclosure will be described with reference to FIG.
  • the basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in this embodiment, only the periphery of the disease analyzer will be described with reference to FIG. 10, and description of other components will not be repeated.
  • the disease risk analysis system 601 of the present embodiment is mainly provided with a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 630.
  • the disease analyzer 630 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In this embodiment, the disease analysis apparatus 630 will be described as applied to an example in which the portable information terminal apparatus owned by the portable subject 50 is used.
  • a control program stored in a non-volatile memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a blood flow data calculation unit 635. At least functions as an input / output interface as an analysis input / output unit 34, and functions as a non-volatile memory as a vascular pulse wave data storage unit 37 and a blood pressure data storage unit 33. .
  • the blood flow data calculation unit 635 calculates blood flow data of the subject 50 based on the blood vessel pulse wave data. Specifically, blood vessel pulse wave data stored in the blood vessel pulse wave data storage unit 37 is called, and blood flow data is calculated based on the called blood vessel pulse wave data. In addition, as a method of calculating blood flow data based on the blood vessel pulse wave data, a known method can be used and is not particularly limited. The calculated blood flow data is associated with blood pressure data calculated from the same vascular pulse wave data and stored in the blood pressure data storage unit 33.
  • the control of the disease risk analysis in the disease analyzer 630 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
  • linked blood flow data is also referred to.
  • FIG. 11 shows an electrical configuration common to the disease information management apparatus 20 and the disease analysis apparatuses 30, 130, 230, 330, 430, 530, and 630 in the first to seventh embodiments described above.
  • the computer system 2 includes a CPU 3, a ROM 4, a RAM 5, a hard disk 6, an input interface 7, and the like.
  • Non-transitory computer-readable media include, for example, magnetic recording media such as flexible disks, magnetic tapes, and hard disks, magneto-optical recording media such as magneto-optical disks, optical recording media such as CD-ROM (Compact Read Only Memory), Including, but not limited to, semiconductor memories such as ROM (Read Only Memory), flash memory, and RAM (Random Access Memory).

Abstract

This disease analysis apparatus is provided with: a blood vessel-related data storage unit that stores blood vessel-related data obtained by successive measurements in a blood vessel-related data measuring unit; a blood pressure data computation unit that calculates blood pressure data on the basis of the blood vessel-related data; a blood pressure data storage unit that stores the calculated blood pressure data; a blood pressure change information computation unit that acquires at least two arbitrary pieces of blood pressure data from the stored blood pressure data, and calculates change information, which is information relating to the amount of change in the at least two acquired pieces of blood pressure data; and a disease analysis unit that refers to a blood pressure disease database in which change information and disease risk information are associated and acquires disease risk information associated with the change information calculated by the blood pressure change information computation unit to analyze a disease risk.

Description

疾患分析装置、疾患リスク分析システムおよび疾患分析プログラムDisease analysis apparatus, disease risk analysis system, and disease analysis program 関連出願の相互参照Cross-reference of related applications
 本国際出願は、2015年 4月10日に日本国特許庁に出願された日本国特許出願第2015-81002号に基づく優先権を主張するものであり、日本国特許出願第2015-81002号の全内容を本国際出願に参照により援用する。 This international application claims priority based on Japanese Patent Application No. 2015-81002 filed with the Japan Patent Office on April 10, 2015, and is based on Japanese Patent Application No. 2015-81002. The entire contents are incorporated by reference into this international application.
 本開示は、疾患分析装置、疾患リスク分析システムおよび疾患分析プログラム記録媒体に関し、例えば、血圧情報等に基づく疾患分析装置、疾患リスク分析システムおよび疾患分析プログラム記録媒体に関する。 The present disclosure relates to a disease analysis device, a disease risk analysis system, and a disease analysis program recording medium, for example, a disease analysis device, a disease risk analysis system, and a disease analysis program recording medium based on blood pressure information and the like.
 カフ式血圧測定器等で測定した血圧値が所定の基準値内に入るか否かに基づき、疾患の分析を行う装置が知られていた。しかしながら、測定した血圧値の絶対値のみ用いる分析では、個人による血圧値の差や、季節による血圧値の差等が存在するため所望の分析精度を実現することは困難であった。 An apparatus for analyzing a disease based on whether or not a blood pressure value measured with a cuff blood pressure measuring instrument falls within a predetermined reference value has been known. However, in the analysis using only the absolute value of the measured blood pressure value, there is a difference in blood pressure value between individuals, a difference in blood pressure value depending on the season, and the like, and it has been difficult to achieve a desired analysis accuracy.
 この問題を解決するために、時間的生物学的リズムの変化等を病態に関連づけ、時間生物学的リズム予測基準により予測したリズムと実際の測定値との乖離および上記関連付けに基づいて切迫疾患の発生を予測するシステムが提案されている(例えば、特許文献1参照。)。 In order to solve this problem, the change of temporal biological rhythm etc. is related to the pathological condition, the difference between the rhythm predicted by the temporal biological rhythm prediction standard and the actual measurement value and the above association of A system for predicting occurrence has been proposed (see, for example, Patent Document 1).
特許第4938855号公報Japanese Patent No. 4938855
 上述の特許文献1に記載された技術では、個人による血圧値の差や、季節による血圧値の差等による分析精度、または予測精度の低下を抑制することが可能となっている。しかしながら、血圧測定器等で測定した血圧値が所定の基準値内に入るか否かに基づき疾患の分析等を行っている点では従来と同様であるため、個人による血圧値の差や、季節による血圧値の差等による影響の排除には限度があり、分析精度、または予測精度の更なる向上を図り難いという問題があった。 In the technique described in Patent Document 1 described above, it is possible to suppress a decrease in analysis accuracy or prediction accuracy due to a difference in blood pressure value among individuals, a difference in blood pressure value due to season, or the like. However, since it is the same as in the past in terms of analyzing the disease based on whether or not the blood pressure value measured with a blood pressure measuring instrument falls within a predetermined reference value, There is a limit in eliminating the influence due to the difference in blood pressure value, etc., and there is a problem that it is difficult to further improve analysis accuracy or prediction accuracy.
 本開示の一局面では、疾患の分析精度向上を図り易くすることができる疾患分析装置、疾患リスク分析システムおよび疾患分析プログラム記録媒体を提供することが望ましい。 In one aspect of the present disclosure, it is desirable to provide a disease analysis apparatus, a disease risk analysis system, and a disease analysis program recording medium that can facilitate improvement of disease analysis accuracy.
 
 本開示の第1の態様に係る疾患分析装置は、血管関連データ計測部において連続的に測定された被検体の血管関連データを記憶する血管関連データ記憶部と、前記血管関連データに基づき、血圧データを算出する血圧データ演算部と、前記血圧データ演算部において算出された前記血圧データを記憶する血圧データ記憶部と、少なくとも前記血圧データ記憶部に記憶された血圧データから、任意の少なくとも二つの血圧データを取得し、取得した前記少なくとも二つの血圧データの変化量に関する情報である変化情報を算出する血圧変化情報演算部と、前記変化情報と疾患リスク情報とが関連付けされた血圧疾患データベースを参照し、前記血圧変化情報演算部により算出された前記変化情報に関連付けされた前記疾患リスク情報を取得して疾患リスクを分析する疾患分析部と、を備える。

The disease analysis apparatus according to the first aspect of the present disclosure includes a blood vessel related data storage unit that stores blood vessel related data of a subject continuously measured in a blood vessel related data measurement unit, and a blood pressure based on the blood vessel related data. A blood pressure data calculation unit for calculating data, a blood pressure data storage unit for storing the blood pressure data calculated in the blood pressure data calculation unit, and at least two arbitrary blood pressure data stored in the blood pressure data storage unit Refers to a blood pressure change information calculation unit that acquires blood pressure data, calculates change information that is information relating to the amount of change of the acquired at least two blood pressure data, and a blood pressure disease database in which the change information and disease risk information are associated And acquiring the disease risk information associated with the change information calculated by the blood pressure change information calculation unit. We include a disease analyzer for analyzing the patient risks, and.
 本開示の第2の態様に係る疾患リスク分析システムは、被検体の血管関連データを計測する血管関連データ計測部を備えた生体情報取得装置と、少なくとも二つの血圧データの変化量に関する情報である変化情報と疾患リスク情報とが関連付けされた血圧疾患データベースを備えた疾患情報管理装置と、前記血管関連データ計測部において連続的に測定された前記被検体の前記血管関連データを記憶する血管関連データ記憶部と、前記血管関連データに基づき、前記血圧データを算出する血圧データ演算部と、前記血圧データ演算部において算出された前記血圧データ記憶部と、前記血圧データ記憶部に記憶された前記血圧データから任意の少なくとも二つの血圧データを取得し、取得した前記少なくとも二つの血圧データに関する前記変化情報を算出する血圧変化情報演算部と、前記血圧疾患データベースを参照し、前記変化情報に関連付けされた前記疾患リスク情報を取得して疾患リスクを分析する疾患分析部と、を備えた、疾患分析装置と、を有する。 The disease risk analysis system according to the second aspect of the present disclosure is information related to a biological information acquisition device including a blood vessel-related data measurement unit that measures blood vessel-related data of a subject, and changes in at least two blood pressure data. Blood vessel related data for storing the blood vessel related data of the subject continuously measured in the blood vessel related data measuring unit, and a disease information management device having a blood pressure disease database in which change information and disease risk information are associated A blood pressure data calculation unit that calculates the blood pressure data based on the blood vessel related data, the blood pressure data storage unit calculated in the blood pressure data calculation unit, and the blood pressure stored in the blood pressure data storage unit Any at least two blood pressure data are acquired from the data, and the change relating to the acquired at least two blood pressure data is performed. A disease analysis comprising: a blood pressure change information calculation unit that calculates information; and a disease analysis unit that references the blood pressure disease database and acquires the disease risk information associated with the change information and analyzes the disease risk And a device.
 本開示の第3の態様に係る非一時的コンピュータ可読媒体に格納される疾患分析プログラムは、コンピュータに、血管関連データ計測部において異なる時間に測定された少なくとも二つの血管関連データに基づく血圧データを取得し、取得した前記少なくとも二つの血圧データの変化量に関する情報である変化情報を算出する血圧変化情報演算機能と、前記変化情報と疾患リスク情報とが関連付けされた血圧疾患データベースを参照し、前記変化情報に関連付けされた前記疾患リスク情報を取得して疾患リスクを分析する疾患分析機能と、を実現させる。 A disease analysis program stored in a non-transitory computer-readable medium according to the third aspect of the present disclosure is a computer that stores blood pressure data based on at least two blood vessel-related data measured at different times in a blood vessel-related data measurement unit. Referring to the blood pressure disease database in which the change information and the disease risk information are associated with each other, and the blood pressure change information calculation function for calculating change information that is information relating to the amount of change in the acquired at least two blood pressure data. And a disease analysis function for obtaining the disease risk information associated with the change information and analyzing the disease risk.
 本開示の第1の態様に係る疾患分析装置、第2の態様に係る疾患リスク分析システム、第3の態様に係る疾患分析プログラムによれば、任意の少なくとも二つの血圧データの変化量に関する情報(以下、「変化情報」とも表記する。)、および、変化情報と関連付けされた疾患リスクの情報に基づいて疾患リスクの分析が行われる。そのため、血圧データの絶対値に基づいて疾患リスクを分析する場合と比較して、個人による血圧値の差や、季節による血圧値の差等による影響の排除した分析を行いやすくなる。なお、疾患リスクと変化情報との関連付けとしては、統計的な処理に基づく関連付けを例示することができる。 According to the disease analysis apparatus according to the first aspect of the present disclosure, the disease risk analysis system according to the second aspect, and the disease analysis program according to the third aspect, information on the amount of change in any at least two blood pressure data ( Hereinafter, the disease risk is also analyzed based on the disease risk information associated with the change information. Therefore, compared with the case of analyzing the disease risk based on the absolute value of the blood pressure data, it becomes easier to perform an analysis in which the influence due to the difference in blood pressure value among individuals, the difference in blood pressure value depending on the season, and the like is eliminated. In addition, as an association between the disease risk and the change information, an association based on statistical processing can be exemplified.
 本開示の第1の態様に係る疾患分析装置、第2の態様に係る疾患リスク分析システム、第3の態様に係る疾患分析プログラムによれば、変化情報、および、変化情報と関連付けされた疾患リスクの情報に基づいて疾患リスクの分析が行われる。そのため、血圧データの絶対値に基づいて疾患リスクを分析する場合と比較して、疾患の分析精度向上を図り易くなるという効果を奏する。 According to the disease analysis apparatus according to the first aspect of the present disclosure, the disease risk analysis system according to the second aspect, and the disease analysis program according to the third aspect, change information and the disease risk associated with the change information Based on this information, disease risk analysis is performed. Therefore, compared to the case of analyzing the disease risk based on the absolute value of the blood pressure data, there is an effect that it is easy to improve the analysis accuracy of the disease.
本開示の第1の実施形態に係るリスク分析システムの構成を示す摸式図である。It is a model diagram which shows the structure of the risk analysis system which concerns on 1st Embodiment of this indication. 血圧データの測定および記憶処理を説明するフローチャートである。It is a flowchart explaining the measurement and storage process of blood pressure data. 血圧データに基づく疾患リスク分析処理を説明するフローチャートである。It is a flowchart explaining the disease risk analysis process based on blood pressure data. 図1のリスク分析システムの変形例の構成を示す模式図である。It is a schematic diagram which shows the structure of the modification of the risk analysis system of FIG. 本開示の第2の実施形態に係るリスク分析システムの構成を示す摸式図である。It is a model diagram which shows the structure of the risk analysis system which concerns on 2nd Embodiment of this indication. 本開示の第3の実施形態に係るリスク分析システムの構成を示す摸式図である。It is a model diagram which shows the structure of the risk analysis system which concerns on 3rd Embodiment of this indication. 本開示の第4の実施形態に係るリスク分析システムの構成を示す摸式図である。It is a model diagram which shows the structure of the risk analysis system which concerns on 4th Embodiment of this indication. 本開示の第5の実施形態に係るリスク分析システムの構成を示す摸式図である。It is a model diagram which shows the structure of the risk analysis system which concerns on 5th Embodiment of this indication. 本開示の第6の実施形態に係るリスク分析システムの構成を示す摸式図である。It is a model diagram which shows the structure of the risk analysis system which concerns on 6th Embodiment of this indication. 本開示の第7の実施形態に係るリスク分析システムの構成を示す摸式図である。It is a model diagram which shows the structure of the risk analysis system which concerns on 7th Embodiment of this indication. 本開示の疾患情報管理装置及び疾患分析装置に共通する電気的構成を示す模式図である。It is a schematic diagram which shows the electrical structure common to the disease information management apparatus and disease analysis apparatus of this indication.
 1,101,201,301,401,501,601…疾患リスク分析システム、10,110,210…血管モニタ(生体情報取得装置)、11…血管脈波センサ(血管関連データ計測部)、20…疾患情報管理装置、21…血圧疾患データベース、23…個人情報データベース、30,130,230,330,430,530,630…疾患分析装置、31…血圧変化情報演算部、32…疾患分析部、33…血圧データ記憶部、36…血圧データ演算部、37…血管脈波データ記憶部(血管関連データ記憶部)、114…温度計測部、135,235…活動状況判定部(判定部)、214…加速度計測部、335…身体情報入力部、435…生活情報入力部、535…脈拍データ演算部、635…血流データ演算部 1, 101, 201, 301, 401, 501, 601 ... Disease risk analysis system, 10, 110, 210 ... Blood vessel monitor (biological information acquisition device), 11 ... Blood vessel pulse wave sensor (blood vessel related data measuring unit), 20 ... Disease information management device, 21 ... blood pressure disease database, 23 ... personal information database, 30, 130, 230, 330, 430, 530, 630 ... disease analysis device, 31 ... blood pressure change information calculation unit, 32 ... disease analysis unit, 33 ... blood pressure data storage unit, 36 ... blood pressure data calculation unit, 37 ... blood vessel pulse wave data storage unit (blood vessel related data storage unit), 114 ... temperature measurement unit, 135, 235 ... activity status determination unit (determination unit), 214 ... Acceleration measurement unit, 335 ... physical information input unit, 435 ... life information input unit, 535 ... pulse data calculation unit, 635 ... blood flow data calculation unit
〔第1の実施形態〕
 この開示の第1の実施形態に係る疾患リスク分析システム1および疾患分析装置30について、図1から図4を参照しながら説明する。
[First Embodiment]
The disease risk analysis system 1 and the disease analysis device 30 according to the first embodiment of the present disclosure will be described with reference to FIGS. 1 to 4.
 本実施形態に係る疾患リスク分析システム1は、連続的に測定された被検体50の脈波データをベースに算出した血圧データに基づいて被検体50の疾患リスクを分析するシステムであり、疾患分析装置30は、疾患リスク分析システム1に含まれるものである。疾患リスク分析システム1には、図1に示すように、脈波データをベースにした血管モニタ(生体情報取得装置)10と、疾患情報管理装置20と、疾患分析装置30と、が主に設けられている。 The disease risk analysis system 1 according to the present embodiment is a system that analyzes a disease risk of a subject 50 based on blood pressure data calculated based on pulse wave data of the subject 50 that is continuously measured. The device 30 is included in the disease risk analysis system 1. As shown in FIG. 1, the disease risk analysis system 1 is mainly provided with a blood vessel monitor (biological information acquisition device) 10 based on pulse wave data, a disease information management device 20, and a disease analysis device 30. It has been.
 なお、連続的に測定とは、中断なく測定すること、一定間隔をおいて測定することのどちらも含む概念であり、通常は脈拍1拍毎の測定から数時間毎の測定であり、血管モニタ10の消費電力を少なくする観点からは数分から数時間の一定間隔をおいて測定することが好ましい。 Note that continuous measurement is a concept that includes both measurement without interruption and measurement at regular intervals. Usually, the measurement is performed every few hours from one measurement of each pulse, and is a blood vessel monitor. From the viewpoint of reducing the power consumption of 10, it is preferable to measure at regular intervals of several minutes to several hours.
 血管モニタ10は被検体50に取り付けられるものであり、被検体50の血圧を連続して測定するものである。血管モニタ10には、血管脈波センサ(血管関連データ計測部)11と、時間計測部12と、モニタ側入出力部13と、が少なくとも設けられている。 The blood vessel monitor 10 is attached to the subject 50, and continuously measures the blood pressure of the subject 50. The blood vessel monitor 10 is provided with at least a blood vessel pulse wave sensor (blood vessel related data measuring unit) 11, a time measuring unit 12, and a monitor side input / output unit 13.
 血管脈波センサ11は被検体50の血管脈波を連続して計測し、計測した血管脈波の値に関するデータである血管脈波データ(血管関連データ)を出力するものであり、時間計測部12は血管脈波データが計測された時点における時刻の情報である時間情報を出力するものである。モニタ側入出力部13は、血管脈波データと時間情報とを疾患分析装置30に出力するものである。 The blood vessel pulse wave sensor 11 continuously measures the blood vessel pulse wave of the subject 50 and outputs blood vessel pulse wave data (blood vessel related data) that is data relating to the value of the measured blood vessel pulse wave. Reference numeral 12 denotes time information that is time information at the time when the blood vessel pulse wave data is measured. The monitor-side input / output unit 13 outputs vascular pulse wave data and time information to the disease analyzer 30.
 本実施形態では、血管脈波センサ11として、近赤外線などの光を被検体50に照射し、反射または透過した光における位相の変化に基づいて血管脈波を連続的に計測するものに適用して説明する。なお、血管脈波センサ11としては、上述の方式に基づくセンサに限らず、連続して計測可能な他の方式に基づくセンサであってもよく、測定方式を限定するものではない。 In the present embodiment, the vascular pulse wave sensor 11 is applied to a sensor that irradiates the subject 50 with light such as near infrared rays and continuously measures the vascular pulse wave based on a phase change in the reflected or transmitted light. I will explain. The blood vessel pulse wave sensor 11 is not limited to a sensor based on the above-described method, and may be a sensor based on another method that can be continuously measured, and the measurement method is not limited.
 ここで、血管脈波とは、血管脈波センサ11により測定される血管に関する物性値であって、血管の容積等のように心臓の拍動に伴い値が繰り返し変化するものを言う。特に、後述するように、血圧の算出に用いることができるものであることが好ましい。 Here, the vascular pulse wave is a physical property value related to the blood vessel measured by the vascular pulse wave sensor 11, and refers to a value that repeatedly changes with the pulsation of the heart, such as the volume of the blood vessel. In particular, as will be described later, it is preferable that the blood pressure can be used.
 モニタ側入出力部13は、疾患分析装置30との間で情報の送受信を行う通信部である。疾患分析装置30との通信は、有線通信や無線通信であってもよいし、両者を組み合わせたものであってもよい。本実施形態では、疾患分析装置30との間でBluetooth(登録商標)等の低消費電力の短距離無線通信技術を用いて通信を行う例に適用して説明する。なお、通信方法はこれに限定されるものではなく、Wi-Fi等の他の無線通信技術を用いても良い。 The monitor-side input / output unit 13 is a communication unit that transmits and receives information to and from the disease analysis device 30. Communication with the disease analyzer 30 may be wired communication or wireless communication, or may be a combination of both. In the present embodiment, description will be made by applying to an example in which communication with the disease analysis apparatus 30 is performed using a short-range wireless communication technology with low power consumption such as Bluetooth (registered trademark). Note that the communication method is not limited to this, and other wireless communication technologies such as Wi-Fi may be used.
 疾患情報管理装置20は、CPU(中央演算処理ユニット)、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置30と情報通信可能に接続されたデータベースサーバである例に適用して説明する。 The disease information management apparatus 20 is a computer system having a CPU (Central Processing Unit), ROM, RAM, hard disk, input / output interface and the like. In the present embodiment, description will be made by applying to an example of a database server connected to the disease analysis device 30 so as to be capable of information communication.
 ROM等に記憶されている制御プログラムは、ハードディスク等を血圧疾患データベース21として機能させるものであり、入出力インタフェース等を管理側入出力部22として機能させるものであり、CPUを血圧疾患データベース21および管理側入出力部22の動作を制御する制御部として機能させるものである。 The control program stored in the ROM or the like causes the hard disk or the like to function as the blood pressure disease database 21 and causes the input / output interface or the like to function as the management-side input / output unit 22. It functions as a control unit that controls the operation of the management-side input / output unit 22.
 血圧疾患データベース21は、少なくとも後述する差分情報と疾患リスク情報とを統計的に関連付けして記憶するものである。また、記憶された疾患リスク情報は、血圧疾患データベース21から管理側入出力部22を介して疾患分析装置30へ出力可能とされている。 The blood pressure disease database 21 stores at least differential information and disease risk information, which will be described later, in a statistically correlated manner. The stored disease risk information can be output from the blood pressure disease database 21 to the disease analysis device 30 via the management input / output unit 22.
 統計的に関連付けされた差分情報と疾患リスク情報としては、それまでに蓄積された差分情報、および、疾患リスク情報を統計的な処理を行うことにより関連付けした結果であり、予め血圧疾患データベース21に記憶されたものを例示することができる。なお、差分情報と疾患リスク情報との統計的な関連付けは、定期的に更新されるものであってもよい。 The statistically related difference information and disease risk information are the results of associating the difference information accumulated so far and the disease risk information by performing statistical processing, and are stored in the blood pressure disease database 21 in advance. What is stored can be exemplified. Note that the statistical association between the difference information and the disease risk information may be periodically updated.
 管理側入出力部22は、疾患分析装置30との間で情報の送受信を行う通信部である。疾患分析装置30との通信は、有線通信や無線通信であってもよいし、両者を組み合わせたものであってもよい。本実施形態では、疾患情報管理装置20と疾患分析装置30との間に無線基地局が配置され、疾患情報管理装置20と無線基地局との間はインターネットやイントラネットや、LAN(ローカル・エリア・ネットワーク)などの通信設備を利用して通信を行い、無線基地局と疾患分析装置30との間はWi-Fi(登録商標)等の無線通信技術を利用して通信を行う例に適用して説明する。 The management-side input / output unit 22 is a communication unit that transmits and receives information to and from the disease analysis device 30. Communication with the disease analyzer 30 may be wired communication or wireless communication, or may be a combination of both. In the present embodiment, a radio base station is disposed between the disease information management apparatus 20 and the disease analysis apparatus 30, and between the disease information management apparatus 20 and the radio base station, the Internet, an intranet, a LAN (local area network), or the like. Network), etc., and is applied to an example in which communication between the wireless base station and the disease analyzer 30 is performed using wireless communication technology such as Wi-Fi (registered trademark). explain.
 また、疾患分析装置30は、表示部を備えることができる。表示部は、血管モニタ10から送信された血管脈波データ、又は疾患分析装置30の演算結果を表示する装置である。疾患分析装置30の演算結果としては、具体的には後述する血圧データ演算部36及び疾患分析部32の演算結果を表示することができ、血圧、脈拍、血流速度、血流量、脈拍数、血糖値等の生体情報や疾患リスクに関する情報を表示することができる。かかる表示部としては、適当なディスプレイ等を用いることができる。疾患分析装置30は、表示部を備えることで、被験者50が自身の測定結果について即時に生体情報や疾患リスクに関する情報を得ることが可能となる。 Moreover, the disease analyzer 30 can include a display unit. The display unit is a device that displays blood vessel pulse wave data transmitted from the blood vessel monitor 10 or a calculation result of the disease analysis device 30. As the calculation result of the disease analyzer 30, specifically, the calculation results of the blood pressure data calculation unit 36 and the disease analysis unit 32 described later can be displayed, and blood pressure, pulse, blood flow velocity, blood flow rate, pulse rate, It is possible to display biological information such as blood glucose level and information on disease risk. As such a display unit, an appropriate display or the like can be used. By providing the display unit with the disease analysis device 30, the subject 50 can immediately obtain biological information and information on the disease risk regarding his / her measurement results.
 疾患分析装置30は、CPU(中央演算処理ユニット)、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置30が、持ち運び可能な被検体50が所有する携帯端末、例えば携帯型情報端末装置(スマートフォンや、タブレット型PC)である例に適用して説明する。 The disease analyzer 30 is a computer system having a CPU (Central Processing Unit), ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analysis device 30 is a portable terminal owned by a portable subject 50, such as a portable information terminal device (smart phone or tablet PC).
 携帯型情報端末装置の場合、フラッシュメモリなどの不揮発性メモリに記憶されている制御プログラムは、CPUを血圧変化情報演算部31、血圧データ演算部36および疾患分析部32として少なくとも機能させるものであり、入出力インタフェース等を分析側入出力部34として機能させるものであり、不揮発性メモリ等を血管脈波データ記憶部37および血圧データ記憶部33として機能させるものである。 In the case of a portable information terminal device, a control program stored in a non-volatile memory such as a flash memory causes the CPU to function at least as the blood pressure change information calculation unit 31, the blood pressure data calculation unit 36, and the disease analysis unit 32. The input / output interface or the like functions as the analysis-side input / output unit 34, and the nonvolatile memory or the like functions as the blood vessel pulse wave data storage unit 37 and blood pressure data storage unit 33.
 血管脈波データ記憶部37は、血管モニタ10において連続的に測定された血管脈波データ、および、血管脈波データが計測された時点における時間情報が紐付けされて記憶するものである。血管脈波データ記憶部37は、血管モニタ10から入力された血管脈波データおよび時間情報を記憶可能であるとともに、記憶された血管脈波データを血圧データ演算部36に出力可能な構成とされている。 The blood vessel pulse wave data storage unit 37 stores the blood vessel pulse wave data continuously measured by the blood vessel monitor 10 and time information at the time when the blood vessel pulse wave data is measured in association with each other. The vascular pulse wave data storage unit 37 can store the vascular pulse wave data and time information input from the blood vessel monitor 10 and can output the stored vascular pulse wave data to the blood pressure data calculation unit 36. ing.
 血圧データ記憶部33は、血圧データ演算部36により算出された血圧データ、および、血圧データに対応する血管脈波データが計測された時点における時間情報が紐付けされて記憶するものである。血圧データ記憶部33は、血圧データ演算部36から入力された血圧データおよび時間情報を記憶可能であるとともに、記憶された血圧データを血圧変化情報演算部31に出力可能な構成とされている。 The blood pressure data storage unit 33 stores the blood pressure data calculated by the blood pressure data calculation unit 36 and time information at the time when the blood vessel pulse wave data corresponding to the blood pressure data is measured in association with each other. The blood pressure data storage unit 33 can store the blood pressure data and time information input from the blood pressure data calculation unit 36 and can output the stored blood pressure data to the blood pressure change information calculation unit 31.
 血圧データ演算部36は、血管脈波データ記憶部37に記憶された血管脈波データから血圧データを算出するものである。血管脈波データから血圧データを算出する方法としては、公知の算出方法を用いることができ、特に限定するものではない。 The blood pressure data calculation unit 36 calculates blood pressure data from the blood vessel pulse wave data stored in the blood vessel pulse wave data storage unit 37. As a method for calculating blood pressure data from vascular pulse wave data, a known calculation method can be used, and it is not particularly limited.
 血圧変化情報演算部31は、血圧データ記憶部33に記憶された血圧データから少なくとも二つの血圧データを取得し、取得した少なくとも二つの血圧データの変化情報として差分情報を算出するものである。取得される血圧データは、所定の時間情報に紐付けされた複数の血圧データの中から選択されている。なお、本実施形態では、二つの血圧データの変化情報として差分情報を算出する例に適用して説明するが、変化情報は二つの血圧データの変化が分かる情報であればよく、特に差分情報に限定するものではない。 The blood pressure change information calculation unit 31 acquires at least two blood pressure data from the blood pressure data stored in the blood pressure data storage unit 33, and calculates difference information as change information of the acquired at least two blood pressure data. The acquired blood pressure data is selected from a plurality of blood pressure data linked to predetermined time information. In the present embodiment, the difference information is calculated as an example of the change information of the two blood pressure data. However, the change information only needs to be information that indicates the change of the two blood pressure data. It is not limited.
 疾患分析部32は、血圧疾患データベース21を参照し、差分情報に関連付けされた疾患リスク情報を取得して疾患リスクを分析するものである。疾患リスクを分析する手法としては公知の手法を用いることができ、特に限定するものではない。 The disease analysis unit 32 refers to the blood pressure disease database 21, acquires disease risk information associated with the difference information, and analyzes the disease risk. As a method for analyzing a disease risk, a known method can be used, and it is not particularly limited.
 分析側入出力部34は、上述のようにモニタ側入出力部13や、管理側入出力部22との間で情報の送受信を行う通信部である。本実施形態では、分析側入出力部34には、モニタ側入出力部13との通信を行う部分と、管理側入出力部22との通信を行う部分とが設けられている例に適用して説明する。 The analysis-side input / output unit 34 is a communication unit that transmits and receives information to and from the monitor-side input / output unit 13 and the management-side input / output unit 22 as described above. In the present embodiment, the analysis side input / output unit 34 is applied to an example in which a part that communicates with the monitor side input / output unit 13 and a part that communicates with the management side input / output unit 22 are provided. I will explain.
 次に、上記の構成からなる疾患リスク分析システム1における疾患リスク分析について説明する。まず、血管モニタ10により測定された血管脈波データが疾患分析装置30に記憶される際の制御について図2のフローチャートを参照しながら説明する。 Next, disease risk analysis in the disease risk analysis system 1 configured as described above will be described. First, control when blood vessel pulse wave data measured by the blood vessel monitor 10 is stored in the disease analyzer 30 will be described with reference to the flowchart of FIG.
 被検体50に血管モニタ10が取り付けられると、血管脈波センサ11は被検体50の血管脈波を連続して測定し始める(測定ステップ:S11)。血管脈波センサ11からは、測定した血管脈波に対応した出力である血管脈波データを出力する。血管脈波データは、時間計測部12から出力される時刻を表す時間情報とともに、モニタ側入出力部13から疾患分析装置30に向けて送信される(送信ステップ:S12)。 When the blood vessel monitor 10 is attached to the subject 50, the blood vessel pulse wave sensor 11 starts to continuously measure the blood vessel pulse wave of the subject 50 (measurement step: S11). The vascular pulse wave sensor 11 outputs vascular pulse wave data which is an output corresponding to the measured vascular pulse wave. The blood vessel pulse wave data is transmitted from the monitor-side input / output unit 13 to the disease analysis device 30 together with time information indicating the time output from the time measurement unit 12 (transmission step: S12).
 疾患分析装置30では、分析側入出力部34が、血管モニタ10から送信された血管脈波データおよびこれに対応する時間情報を受信する(受信ステップ:S13)。受信された血管脈波データは、これに対応する時間情報に紐付けされ、血管脈波データ記憶部37に記憶される(血管脈波データ記憶ステップ:S14)。血管脈波データ記憶部37への血管脈波データおよび時間情報は、血管モニタ10による被検体50の血管脈波測定が行われる度に記憶されてもよいし、血管脈波の測定が行われるタイミングとは異なるタイミングで記憶されてもよい。 In the disease analysis apparatus 30, the analysis-side input / output unit 34 receives the blood vessel pulse wave data transmitted from the blood vessel monitor 10 and time information corresponding thereto (reception step: S13). The received vascular pulse wave data is linked to the time information corresponding thereto and stored in the vascular pulse wave data storage unit 37 (vascular pulse wave data storage step: S14). The vascular pulse wave data and the time information to the vascular pulse wave data storage unit 37 may be stored every time the vascular pulse wave of the subject 50 is measured by the vascular monitor 10, or the vascular pulse wave is measured. It may be stored at a timing different from the timing.
 異なるタイミングで記憶が行われる場合、例えば、血管モニタ10や疾患分析装置30に設けられたメモリ等の一時記憶部に血管脈波データ等が記憶され、記憶が行われるタイミングで一時記憶部から血管脈波データ記憶部37への血管脈波データおよび時間情報の記憶が行われてもよい。 When storage is performed at different timings, for example, blood vessel pulse wave data or the like is stored in a temporary storage unit such as a memory provided in the blood vessel monitor 10 or the disease analysis device 30, and the blood vessel is transferred from the temporary storage unit at the timing of storage. The blood vessel pulse wave data and time information may be stored in the pulse wave data storage unit 37.
 その後、疾患分析装置30の血圧データ演算部36は、血管脈波データ記憶部37に記憶された血管脈波データから血圧データを算出する処理を行う(血圧データ算出ステップ:S15)。具体的には、血管脈波データ記憶部37から血圧データの算出が行われていない血管脈波データを呼び出す処理と、呼び出した血管脈波データに基づいて血圧データを算出する処理を行う。なお、従来から用いられているカフ型の電子式血圧計により測定された血圧データやカテーテル型観血測定法により測定された血圧データの値を用いて、血圧計の値の補正を行うようにしても良い。 Thereafter, the blood pressure data calculation unit 36 of the disease analysis apparatus 30 performs a process of calculating blood pressure data from the blood vessel pulse wave data stored in the blood vessel pulse wave data storage unit 37 (blood pressure data calculation step: S15). Specifically, processing for calling blood vessel pulse wave data for which blood pressure data is not calculated from the blood vessel pulse wave data storage unit 37 and processing for calculating blood pressure data based on the called blood vessel pulse wave data are performed. It should be noted that the value of the sphygmomanometer is corrected by using the blood pressure data measured by the cuff type electronic sphygmomanometer used conventionally or the value of the blood pressure data measured by the catheter type blood pressure measuring method. May be.
 算出された血圧データは、これに対応する時間情報に紐付けされ、血圧データ記憶部33に記憶される(血圧データ記憶ステップ:S16)。血圧データの算出および記憶の処理は、上述のように血管脈波データの記憶処理に引き続いて連続的に行われてもよいし、血管脈波データの記憶処理とは別に、所定の独自のタイミングで行われてもよく、特に限定するものではない。 The calculated blood pressure data is linked to the time information corresponding to the calculated blood pressure data and stored in the blood pressure data storage unit 33 (blood pressure data storage step: S16). The blood pressure data calculation and storage process may be performed continuously following the blood vessel pulse wave data storage process as described above, or a predetermined unique timing separately from the blood vessel pulse wave data storage process. There is no particular limitation.
 次に、疾患分析装置30において行われる疾患リスク分析の制御について図3のフローチャートを参照しながら説明する。疾患リスク分析は、予め定められたスケジュールに従って自動的に行われてもよいし、外部から入力される分析開始の指示に基づいて行われてもよく、特に分析を開始するタイミングを限定するものではない。 Next, control of disease risk analysis performed in the disease analyzer 30 will be described with reference to the flowchart of FIG. The disease risk analysis may be automatically performed according to a predetermined schedule, or may be performed based on an instruction to start analysis input from the outside, and is not particularly limited in timing for starting the analysis. Absent.
 疾患リスク分析が開始されると、疾患分析装置30の疾患分析部32は、異なる時間に測定された少なくとも二つの血圧データを取得する処理を実行する(血圧データ取得ステップ:S21)。本実施形態では、直近の血圧データ(例えば、一拍前から1時間前の所望のタイミングで測定された血圧データ)と、前日の同じ時間に測定された血圧データ(以下「過去の血圧データ」とも表記する。)を取得する例に適用して説明する。 When the disease risk analysis is started, the disease analysis unit 32 of the disease analysis device 30 executes a process of acquiring at least two blood pressure data measured at different times (blood pressure data acquisition step: S21). In the present embodiment, the latest blood pressure data (for example, blood pressure data measured at a desired timing one hour before one beat) and blood pressure data measured at the same time on the previous day (hereinafter “past blood pressure data”). This is also applied to an example of acquiring.
 なお、過去の血圧データとして、上述のような前日の同じ時間に測定された血圧データの代わりに、数分前、数時間前のように同日内(24時間以内)に測定された血圧データを用いてもよく特に限定されるものではない。数分前、数時間前の過去の血圧データを利用することで、被検体50の例えば、早朝時、午前、午後、夕方、夜間、就寝中等の日内の血圧変動を詳細に把握しやすくなり、疾患の分析精度向上を図り易くすることができる。また、過去の血圧データとしては、前週、前月、前年の所定日における同じ時間のように、さらに過去に遡ったタイミングで測定された血圧データを用いてもよく、特に限定するものではない。前週、前月、前年などの過去の血圧データを利用可能とすることで、被検体50の過去からの状態変化を把握しやすくなり、疾患の分析精度向上を図り易くすることができる。 As the past blood pressure data, instead of the blood pressure data measured at the same time on the previous day as described above, blood pressure data measured within the same day (within 24 hours), such as several minutes ago and several hours ago. It may be used and is not particularly limited. By using the past blood pressure data several minutes ago and several hours ago, it becomes easier to grasp in detail blood pressure fluctuations in the subject 50 such as early morning, morning, afternoon, evening, nighttime, sleeping, etc. It is possible to easily improve the accuracy of disease analysis. Further, as the blood pressure data in the past, blood pressure data measured at a timing further back in the past, such as the same time on the predetermined day of the previous week, the previous month, or the previous year, may be used, and is not particularly limited. By making it possible to use past blood pressure data such as the previous week, the previous month, and the previous year, it becomes easy to grasp the state change of the subject 50 from the past, and it is possible to easily improve the analysis accuracy of the disease.
 また、直近の血圧データおよび過去の血圧データは、複数の血圧データに基づいて求められた平均の血圧データであってもよい。例えば、一拍前から1時間前の所望の複数タイミングで測定された数個分の血圧データの平均値や、前日までの数日から1年の期間における同じ時間に測定された数個分の血圧データの平均値であってもよい。 Further, the latest blood pressure data and the past blood pressure data may be average blood pressure data obtained based on a plurality of blood pressure data. For example, the average value of several blood pressure data measured at desired multiple timings one hour before one beat, or several pieces measured at the same time in the period from several days up to the previous day It may be an average value of blood pressure data.
 その後、血圧変化情報演算部31は、二つの血圧データの変化量に関する変化情報として、取得した二つの血圧データの差分値である差分情報を算出する処理を行う(血圧変化情報演算ステップ:S22)。算出された差分情報は、分析側入出力部34から疾患情報管理装置20の管理側入出力部22へ出力される。 Thereafter, the blood pressure change information calculation unit 31 performs a process of calculating difference information, which is a difference value between the acquired two blood pressure data, as change information regarding the change amount of the two blood pressure data (blood pressure change information calculation step: S22). . The calculated difference information is output from the analysis side input / output unit 34 to the management side input / output unit 22 of the disease information management apparatus 20.
 疾患情報管理装置20は、血圧疾患データベース21に記憶された疾患リスク情報であって、入力された差分情報と同じ値を持つ差分情報に紐付けされた疾患リスク情報を選択する処理を行う(疾患リスク情報選択ステップ:S23)。選択された疾患リスク情報は、管理側入出力部22から疾患分析装置30の分析側入出力部34へ出力される。 The disease information management device 20 performs a process of selecting disease risk information stored in the blood pressure disease database 21 and associated with the difference information having the same value as the input difference information (disease) Risk information selection step: S23). The selected disease risk information is output from the management-side input / output unit 22 to the analysis-side input / output unit 34 of the disease analyzer 30.
 疾患分析装置30の疾患分析部32は、取得した疾患リスク情報に基づいて、被検体50の疾患リスクを分析する演算処理を行う(疾患分析ステップ:S24)。分析により求められた疾患リスクは、疾患分析装置30から外部に出力される。出力先としては、例えば、被検体50に疾患リスクを伝えるディスプレイなどの表示装置であってもよいし、被検体50が通院している医療機関に設置されたサーバ等の情報処理装置であってもよい。 The disease analysis unit 32 of the disease analysis device 30 performs a calculation process for analyzing the disease risk of the subject 50 based on the acquired disease risk information (disease analysis step: S24). The disease risk obtained by the analysis is output from the disease analyzer 30 to the outside. The output destination may be, for example, a display device such as a display that conveys a disease risk to the subject 50, or an information processing device such as a server installed in a medical institution where the subject 50 visits. Also good.
 上記の構成の疾患リスク分析システム1および疾患分析装置30によれば、任意の少なくとも二つの血圧データの差分情報、および、当該差分情報と統計的に関連付けされた疾患リスクの情報に基づいて疾患リスクの分析が行われる。そのため、血圧データの絶対値に基づいて疾患リスクを分析する場合と比較して、被検体50個人による血圧値の差や、季節による血圧値の差等による影響の排除した分析を行いやすくなり、疾患の分析精度向上を図り易くすることができる。 According to the disease risk analysis system 1 and the disease analysis device 30 configured as described above, the disease risk based on the difference information of any at least two blood pressure data and the disease risk information statistically associated with the difference information. Analysis is performed. Therefore, compared with the case of analyzing the disease risk based on the absolute value of blood pressure data, it becomes easier to perform an analysis that excludes the effects of differences in blood pressure values by 50 subjects, blood pressure values by season, etc. It is possible to easily improve the accuracy of disease analysis.
 例えば、早朝の高血圧は脳卒中リスクに関連していることが知られており、早朝時の血圧の変動や日間差に基づいて脳卒中リスクを分析することにより、疾患の分析精度向上を図り易くすることができる。また、日中のストレス性高血圧は心臓病や脳卒中リスクに関連していることが知られており、日中時の血圧の変動や日間差に基づいて心臓病や脳卒中リスクを分析することにより、疾患の分析精度向上を図り易くすることができる。さらに、夜間の高血圧は糖尿病リスクに関連していることが知られており、夜間時の血圧の変動や日間差に基づいて糖尿病リスクを分析することにより、疾患の分析精度向上を図り易くすることができる。 For example, early morning hypertension is known to be related to stroke risk, and it is easier to improve the accuracy of disease analysis by analyzing stroke risk based on blood pressure fluctuations and daily differences in the early morning. Can do. In addition, it is known that daytime stress hypertension is related to heart disease and stroke risk, and by analyzing the risk of heart disease and stroke based on fluctuations in blood pressure during the day and daily differences, It is possible to easily improve the accuracy of disease analysis. Furthermore, it is known that nighttime hypertension is related to diabetes risk, and it is easier to improve the accuracy of disease analysis by analyzing diabetes risk based on fluctuations in blood pressure during nighttime and daily differences. Can do.
 血圧データ記憶部33において、血圧データに時間情報を紐付けして記憶することにより、時間情報に関連した差分情報を求めることができる。例えば、時間情報に基づいて取得する血圧データを選択し、選択した血圧データに基づいて差分情報を求めることができる。選択に用いる時間情報は任意に設定することが可能とされ、所望の時間情報に関連した変化情報を求めることが可能となる。 In the blood pressure data storage unit 33, the difference information related to the time information can be obtained by associating and storing the time information with the blood pressure data. For example, blood pressure data acquired based on time information can be selected, and difference information can be obtained based on the selected blood pressure data. Time information used for selection can be arbitrarily set, and change information related to desired time information can be obtained.
 過去の血圧データとして、直近の血圧データに紐付けされた時刻と、同じ時刻に測定されたデータを用いることで、一日の生活リズムによる血圧データの変動の影響を考慮しやすくなり、疾患の分析精度向上を図り易くすることができる。また、前日や、前週、前月、前年などの過去の血圧データを利用可能とすることで、被検体50の過去からの状態変化を把握しやすくなり、疾患の分析精度向上を図り易くすることができる。 By using data measured at the same time as the time associated with the latest blood pressure data as past blood pressure data, it becomes easier to consider the influence of fluctuations in blood pressure data due to daily life rhythm, The analysis accuracy can be improved easily. Further, by making it possible to use past blood pressure data such as the previous day, the previous week, the previous month, the previous year, etc., it becomes easier to grasp the state change of the subject 50 from the past, and it is easy to improve the analysis accuracy of the disease. it can.
 さらに、直近の血圧データおよび過去の血圧データとして複数の血圧データに基づいて求められた平均の血圧データを利用可能とすることで、個々の血圧データに含まれる外部環境等に起因するバラツキの影響を抑制し、疾患の分析精度向上を図り易くすることができる。 Furthermore, by making it possible to use the average blood pressure data obtained based on a plurality of blood pressure data as the latest blood pressure data and the past blood pressure data, the influence of variations caused by the external environment etc. included in each blood pressure data Can be suppressed, and the analysis accuracy of the disease can be easily improved.
 なお、上述の実施形態における疾患情報管理装置20に、図4に示すように、被検体50に関する管理IDや、パスワードや、疾患分析情報に関する属性データが格納された個人情報データベース23が設けられていてもよい。 In addition, as shown in FIG. 4, the disease information management apparatus 20 in the above-described embodiment is provided with a personal information database 23 in which a management ID related to the subject 50, a password, and attribute data related to disease analysis information are stored. May be.
 この場合、S24における被検体50の疾患リスクを分析する演算処理の際に、個人情報データベース23に格納された属性データを利用することにより、血圧疾患データベース21から被検体50に関連付けられた疾患リスク情報を利用することが可能となる。その結果、属性データを利用しない場合と比較して、疾患の分析精度向上を図り易くすることができる。 In this case, the disease risk associated with the subject 50 from the blood pressure disease database 21 by using the attribute data stored in the personal information database 23 in the calculation process for analyzing the disease risk of the subject 50 in S24. Information can be used. As a result, compared with the case where attribute data is not used, it is possible to easily improve the accuracy of disease analysis.
 また、血管モニタ10には、血管モニタ10が被検体50に装着されたか否かを検出し、被検体50に装着された際にはON信号を出力し、被検体50から取り外された際にはOFF信号を出力するセンサが設けられていてもよい。このようなON・OFF信号を疾患分析装置30へ送信することにより、血管モニタ10が被検体50から取り外された際に送信された血圧データが疾患リスク分析に用いられることを抑制できる。 Further, the blood vessel monitor 10 detects whether or not the blood vessel monitor 10 is attached to the subject 50, and outputs an ON signal when the blood vessel monitor 10 is attached to the subject 50, and when the blood vessel monitor 10 is detached from the subject 50. May be provided with a sensor that outputs an OFF signal. By transmitting such an ON / OFF signal to the disease analyzer 30, it is possible to prevent blood pressure data transmitted when the blood vessel monitor 10 is removed from the subject 50 from being used for disease risk analysis.
 なお、上述の実施形態では、血管モニタ10が、血管脈波を測定して血管脈波データを出力する例に適用して説明したが、血圧を含む脈拍や血流などの値の算出が可能な物性値を測定して、そのデータを出力するものであればよく、測定対象を限定するものではない。
〔第2の実施形態〕
 次に、本開示の第2の実施形態について図5を参照して説明する。本実施形態の疾患リスク分析システムの基本構成は、第1の実施形態と同様であるが、第1の実施形態とは、血管モニタおよび疾患分析装置の構成が異なっている。よって、本実施形態においては、図5を用いて血管モニタおよび疾患分析装置の周辺のみを説明し、その他の構成要素等の説明を繰り返さない。
In the above-described embodiment, the blood vessel monitor 10 is described as applied to an example in which the blood vessel pulse wave is measured and the blood vessel pulse wave data is output. However, values such as a pulse including blood pressure and blood flow can be calculated. What is necessary is just to measure various physical property values and output the data, and does not limit the measurement object.
[Second Embodiment]
Next, a second embodiment of the present disclosure will be described with reference to FIG. The basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configurations of the blood vessel monitor and the disease analysis device are different from those of the first embodiment. Therefore, in the present embodiment, only the periphery of the blood vessel monitor and the disease analysis apparatus will be described using FIG. 5, and description of other components will not be repeated.
 本実施形態の疾患リスク分析システム101には、図5に示すように、血管モニタ(生体情報取得装置)110と、疾患情報管理装置20と、疾患分析装置130と、が主に設けられている。 As shown in FIG. 5, the disease risk analysis system 101 of the present embodiment is mainly provided with a blood vessel monitor (biological information acquisition device) 110, a disease information management device 20, and a disease analysis device 130. .
 血管モニタ110は被検体50に取り付けられるものである。血管モニタ110には、血管脈波センサ11と、時間計測部12と、モニタ側入出力部13と、温度計測部(温度計測部)114と、が少なくとも設けられている。 The blood vessel monitor 110 is attached to the subject 50. The blood vessel monitor 110 is provided with at least a blood vessel pulse wave sensor 11, a time measurement unit 12, a monitor side input / output unit 13, and a temperature measurement unit (temperature measurement unit) 114.
 温度計測部114は、血管モニタ110が取り付けられた被検体50の温度、例えば体表面の温度を測定するセンサである。測定された被検体50の体表面の温度は、温度に関連する温度情報として温度計測部114からモニタ側入出力部13を介して疾患分析装置130へ送信される。 The temperature measuring unit 114 is a sensor that measures the temperature of the subject 50 to which the blood vessel monitor 110 is attached, for example, the temperature of the body surface. The measured temperature of the body surface of the subject 50 is transmitted from the temperature measurement unit 114 to the disease analysis device 130 via the monitor side input / output unit 13 as temperature information related to the temperature.
 本実施形態における血管モニタ110が取り付けられる位置は、被検体50の心臓に近い位置が例示される。被検体50の心臓に近い位置に血管モニタ110を取り付けることにより、被検体50の姿勢による血圧変化の影響を抑制することができる。また、血管モニタ110を取り付ける場所は、胸部の冠動脈の直上に対応する体表面であることが望ましい。 The position where the blood vessel monitor 110 is attached in this embodiment is exemplified by a position close to the heart of the subject 50. By attaching the blood vessel monitor 110 at a position close to the heart of the subject 50, the influence of the blood pressure change due to the posture of the subject 50 can be suppressed. Further, the place where the blood vessel monitor 110 is attached is desirably a body surface corresponding to the chest coronary artery.
 疾患分析装置130は、CPU、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置130が、持ち運び可能な被検体50が所有する携帯型情報端末装置である例に適用して説明する。 The disease analyzer 130 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 130 is a portable information terminal device owned by a portable subject 50.
 携帯型情報端末装置の場合、フラッシュメモリなどの不揮発性メモリに記憶されている制御プログラムは、CPUを血圧変化情報演算部31、血圧データ演算部36、疾患分析部32および活動状況判定部(判定部)135として少なくとも機能させるものであり、入出力インタフェース等を分析側入出力部34として機能させるものであり、不揮発性メモリ等を血管脈波データ記憶部37および血圧データ記憶部33として機能させるものである。 In the case of a portable information terminal device, a control program stored in a non-volatile memory such as a flash memory uses a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and an activity status determination unit (determination). Part) 135 and at least functions as an input / output interface 34 as an analysis-side input / output part 34 and functions as a vascular pulse wave data storage part 37 and a blood pressure data storage part 33. Is.
 活動状況判定部135は、血管モニタ110の温度計測部114から入力された体表面の温度情報に基づいて、被検体50の活動状況を判定するものであり、判定結果である活動状態情報を出力するものである。活動状態情報は、温度情報の測定と同じ時期に測定された血圧データと紐付けされて血圧データ記憶部33に記憶される。 The activity status determination unit 135 determines the activity status of the subject 50 based on the temperature information on the body surface input from the temperature measurement unit 114 of the blood vessel monitor 110, and outputs the activity status information that is the determination result. To do. The activity state information is stored in the blood pressure data storage unit 33 in association with blood pressure data measured at the same time as the temperature information measurement.
 ここで、活動状況判定部135における温度情報に基づく被検体50の活動状況の判定について説明する。一般に、人間はその活動状況に応じて体温が変動することが知られている。この体温の値や、変動に基づいて活動状況を判定することができる。例えば、人間の体温は、入眠後に急激に低下し、その後、目覚める頃に上昇することが知られている。この温度変化を利用することにより、被検体50が睡眠状態か否かを推定することが可能となる。 Here, determination of the activity status of the subject 50 based on the temperature information in the activity status determination unit 135 will be described. In general, it is known that a human body temperature fluctuates according to the activity state. The activity status can be determined based on the value of the body temperature and the fluctuation. For example, it is known that a human body temperature rapidly decreases after falling asleep and then increases when the user awakes. By utilizing this temperature change, it is possible to estimate whether or not the subject 50 is in a sleep state.
 本実施形態の疾患分析装置130における疾患リスク分析の制御は、第1の実施形態と比較して、血圧データの変化情報を求める際に用いられる血圧データの取得処理が異なっている。 The control of the disease risk analysis in the disease analyzer 130 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
 つまり本実施形態では、血圧データを取得する際に、紐付けされた活動状態情報も参照される。例えば、睡眠状態などのように同じ活動状態情報に紐付けられた複数の血圧データの中から、変化情報の算出に用いられる血圧データを取得する処理が行われる。 That is, in the present embodiment, the associated activity state information is also referred to when acquiring blood pressure data. For example, a process of acquiring blood pressure data used for calculation of change information from a plurality of blood pressure data associated with the same activity state information such as a sleep state is performed.
 上記の構成の疾患リスク分析システム101および疾患分析装置130によれば、被検体50の活動状態情報にも基づいて疾患リスク分析が行われるため、疾患の分析精度向上を図り易くすることができる。つまり、睡眠状態と覚醒状態のように、取得される血圧データが大きく異なる状態で取得された血圧データの両者を用いた疾患リスク分析の場合、分析精度の低下が発生しやすい。上述のように、活動状態情報にも基づくことで、例えば、睡眠状態で取得された血圧データのみを用いた疾患リスク分析の場合が可能となり、疾患の分析精度向上を図り易くなる。
〔第3の実施形態〕
 次に、本開示の第3の実施形態について図6を参照して説明する。
According to the disease risk analysis system 101 and the disease analysis device 130 configured as described above, the disease risk analysis is performed based also on the activity state information of the subject 50, so that it is possible to easily improve the analysis accuracy of the disease. That is, in the case of disease risk analysis using both blood pressure data acquired in a state where the acquired blood pressure data is significantly different, such as a sleep state and a wakefulness state, the analysis accuracy is likely to decrease. As described above, based on the activity state information, for example, the case of disease risk analysis using only blood pressure data acquired in the sleep state is possible, and it becomes easy to improve the analysis accuracy of the disease.
[Third Embodiment]
Next, a third embodiment of the present disclosure will be described with reference to FIG.
 本実施形態の疾患リスク分析システムの基本構成は、第1の実施形態と同様であるが、第1の実施形態とは、血管モニタおよび疾患分析装置の構成が異なっている。よって、本実施形態においては、図6を用いて血管モニタおよび疾患分析装置の周辺のみを説明し、その他の構成要素等の説明を繰り返さない。 The basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configurations of the blood vessel monitor and the disease analysis device are different from those of the first embodiment. Therefore, in the present embodiment, only the periphery of the blood vessel monitor and the disease analysis apparatus will be described using FIG. 6, and description of other components will not be repeated.
 本実施形態の疾患リスク分析システム201には、図6に示すように、血管モニタ(生体情報取得装置)210と、疾患情報管理装置20と、疾患分析装置230と、が主に設けられている。 As shown in FIG. 6, the disease risk analysis system 201 of the present embodiment is mainly provided with a blood vessel monitor (biological information acquisition device) 210, a disease information management device 20, and a disease analysis device 230. .
 血管モニタ110は被検体50に取り付けられるものである。血管モニタ110には、血管脈波センサ11と、時間計測部12と、モニタ側入出力部13と、加速度計測部(加速度計測部)214と、が少なくとも設けられている。 The blood vessel monitor 110 is attached to the subject 50. The blood vessel monitor 110 is provided with at least a blood vessel pulse wave sensor 11, a time measurement unit 12, a monitor-side input / output unit 13, and an acceleration measurement unit (acceleration measurement unit) 214.
 加速度計測部214は、血管モニタ210が取り付けられた被検体50の体の動きを加速度として測定する三軸の加速度センサである。測定された被検体50の加速度は、加速度に関連する加速度情報として加速度計測部214からモニタ側入出力部13を介して疾患分析装置230へ送信される。 The acceleration measuring unit 214 is a triaxial acceleration sensor that measures the movement of the body of the subject 50 to which the blood vessel monitor 210 is attached as acceleration. The measured acceleration of the subject 50 is transmitted from the acceleration measuring unit 214 to the disease analyzer 230 via the monitor side input / output unit 13 as acceleration information related to the acceleration.
 疾患分析装置230は、CPU、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置230が、持ち運び可能な被検体50が所有する携帯型情報端末装置である例に適用して説明する。 The disease analyzer 230 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 230 is a portable information terminal device owned by a portable subject 50.
 携帯型情報端末装置の場合、フラッシュメモリなどの不揮発性メモリに記憶されている制御プログラムは、CPUを血圧変化情報演算部31、血圧データ演算部36、疾患分析部32および活動状況判定部(判定部)235として少なくとも機能させるものであり、入出力インタフェース等を分析側入出力部34として機能させるものであり、不揮発性メモリを血管脈波データ記憶部37および血圧データ記憶部33として機能させるものである。 In the case of a portable information terminal device, a control program stored in a non-volatile memory such as a flash memory uses a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and an activity status determination unit (determination). Part) 235 to function as at least, input / output interface or the like to function as analysis side input / output part 34, and non-volatile memory to function as vascular pulse wave data storage part 37 and blood pressure data storage part 33 It is.
 活動状況判定部235は、血管モニタ210の加速度計測部214から入力された身体の加速度情報に基づいて、被検体50の活動状況を判定するものであり、判定結果である活動状態情報を出力するものである。活動状態情報は、加速度情報の測定と同じ時期に測定された血圧データと紐付けされて血圧データ記憶部33に記憶される。 The activity status determination unit 235 determines the activity status of the subject 50 based on the body acceleration information input from the acceleration measurement unit 214 of the blood vessel monitor 210, and outputs the activity status information as the determination result. Is. The activity state information is stored in the blood pressure data storage unit 33 in association with blood pressure data measured at the same time as the measurement of acceleration information.
 ここで、活動状況判定部235における加速度情報に基づく被検体50の活動状況の判定について説明する。一般に、人間はその活動状況に応じて体の動かし方、言い換えると加速度の値が変動することが知られている。この加速度の値や、変動に基づいて活動状況を判定することができる。例えば、人間は、睡眠状態において体の動きがおおよそ止まることが知られている。そのため、加速度の値の振動幅が所定振幅範囲に収まるか否かに基づいて、被検体50が睡眠状態か否かを推定することが可能となる。 Here, the determination of the activity status of the subject 50 based on the acceleration information in the activity status determination unit 235 will be described. In general, it is known that humans move their bodies according to their activity status, in other words, the value of acceleration varies. The activity status can be determined based on the acceleration value and the fluctuation. For example, it is known that human beings generally stop moving in a sleep state. Therefore, it is possible to estimate whether or not the subject 50 is in a sleep state based on whether or not the vibration width of the acceleration value falls within the predetermined amplitude range.
 その他にも、加速度情報に基づいて被検体50の歩いている、走っている等の運動状態や、首を動かす、腕を動かす、足を動かすなどの局所的な動き状態を判定することも可能となる。このような活動状態および時間の経過等の複数の情報を組み合わせて判断することにより、被検体50が、電車、エレベータ、車両等の移動デバイスを用いて移動している最中か、歩行中、走行中、デスクワーク中、就寝中か、などの判定が可能となる。 In addition, based on the acceleration information, it is possible to determine the movement state of the subject 50 such as walking and running, and the local movement state such as moving the neck, moving the arm, moving the foot, etc. It becomes. By determining by combining a plurality of information such as the activity state and the passage of time, the subject 50 is moving while using a moving device such as a train, an elevator, or a vehicle, or walking, It is possible to determine whether the vehicle is running, desk work, or sleeping.
 本実施形態の疾患分析装置230における疾患リスク分析の制御は、第1の実施形態と比較して、血圧データの変化情報を求める際に用いられる血圧データの取得処理が異なっている。 The control of the disease risk analysis in the disease analyzer 230 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
 つまり本実施形態では、血圧データを取得する際に、紐付けされた活動状態情報も参照される。例えば、睡眠状態などのように同じ活動状態情報に紐付けられた複数の血圧データの中から、変化情報の算出に用いられる血圧データを取得する処理が行われる。 That is, in the present embodiment, the associated activity state information is also referred to when acquiring blood pressure data. For example, a process of acquiring blood pressure data used for calculation of change information from a plurality of blood pressure data associated with the same activity state information such as a sleep state is performed.
 上記の構成の疾患リスク分析システム201および疾患分析装置230によれば、上述の第1の実施形態、第2の実施形態と比較して、被検体50の活動状態をより細かく判定することができるため、疾患の分析精度向上を更に図り易くなる。
〔第4の実施形態〕
 次に、本開示の第4の実施形態について図7を参照して説明する。本実施形態の疾患リスク分析システムの基本構成は、第1の実施形態と同様であるが、第1の実施形態とは、疾患分析装置の構成が異なっている。よって、本実施形態においては、図7を用いて疾患分析装置の周辺のみを説明し、その他の構成要素等の説明を繰り返さない。
According to the disease risk analysis system 201 and the disease analysis device 230 configured as described above, the activity state of the subject 50 can be determined more finely than in the first embodiment and the second embodiment described above. Therefore, it becomes easier to improve the analysis accuracy of the disease.
[Fourth Embodiment]
Next, a fourth embodiment of the present disclosure will be described with reference to FIG. The basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in this embodiment, only the periphery of the disease analyzer will be described with reference to FIG. 7, and description of other components and the like will not be repeated.
 本実施形態の疾患リスク分析システム301には、図7に示すように、血管モニタ10と、疾患情報管理装置20と、疾患分析装置330と、が主に設けられている。
 疾患分析装置330は、CPU、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置330が、持ち運び可能な被検体50が所有する携帯型情報端末装置である例に適用して説明する。
As shown in FIG. 7, the disease risk analysis system 301 of the present embodiment is mainly provided with a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 330.
The disease analyzer 330 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 330 is a portable information terminal device owned by a portable subject 50.
 携帯型情報端末装置の場合、フラッシュメモリなどの不揮発性メモリに記憶されている制御プログラムは、CPUを血圧変化情報演算部31、血圧データ演算部36、疾患分析部32および身体情報入力部335として少なくとも機能させるものであり、入出力インタフェース等を分析側入出力部34として機能させるものであり、不揮発性メモリ等を血管脈波データ記憶部37および血圧データ記憶部33として機能させるものである。 In the case of a portable information terminal device, a control program stored in a non-volatile memory such as a flash memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a physical information input unit 335. At least it is made to function, and an input / output interface or the like is made to function as the analysis side input / output unit 34, and a nonvolatile memory or the like is made to function as the blood vessel pulse wave data storage unit 37 and the blood pressure data storage unit 33.
 身体情報入力部335は、被検体50の性別や、身長や、体重や体脂肪率などの身体情報の入力に用いられるものである。入力された身体情報は、例えば、疾患分析装置330のハードディスクに記憶され、疾患分析部32における疾患リスク分析の際に読み出されて分析に用いられる。 The body information input unit 335 is used to input body information such as the gender, height, weight, and body fat percentage of the subject 50. The input physical information is stored in, for example, the hard disk of the disease analysis device 330, and is read out and used for analysis in the disease risk analysis in the disease analysis unit 32.
 上記の構成の疾患リスク分析システム301および疾患分析装置330によれば、上述の第1の実施形態等と比較して、被検体50の身体情報を考慮した疾患リスク分析が行えるため、疾患の分析精度向上を更に図り易くなる。
〔第5の実施形態〕
 次に、本開示の第5の実施形態について図8を参照して説明する。本実施形態の疾患リスク分析システムの基本構成は、第1の実施形態と同様であるが、第1の実施形態とは、疾患分析装置の構成が異なっている。よって、本実施形態においては、図8を用いて疾患分析装置の周辺のみを説明し、その他の構成要素等の説明を繰り返さない。
According to the disease risk analysis system 301 and the disease analysis device 330 having the above-described configuration, the disease risk analysis can be performed in consideration of the body information of the subject 50 as compared with the first embodiment described above, and thus the disease analysis It becomes easier to improve accuracy.
[Fifth Embodiment]
Next, a fifth embodiment of the present disclosure will be described with reference to FIG. The basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in this embodiment, only the periphery of the disease analyzer will be described using FIG. 8, and description of other components and the like will not be repeated.
 本実施形態の疾患リスク分析システム401には、図8に示すように、血管モニタ10と、疾患情報管理装置20と、疾患分析装置430と、が主に設けられている。
 疾患分析装置430は、CPU、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置430が、持ち運び可能な被検体50が所有する携帯型情報端末装置である例に適用して説明する。
In the disease risk analysis system 401 of this embodiment, as shown in FIG. 8, a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 430 are mainly provided.
The disease analyzer 430 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, description will be made by applying to an example in which the disease analyzer 430 is a portable information terminal device owned by a portable subject 50.
 携帯型情報端末装置の場合、フラッシュメモリなどの不揮発性メモリに記憶されている制御プログラムは、CPUを血圧変化情報演算部31、血圧データ演算部36、疾患分析部32および生活情報入力部435として少なくとも機能させるものであり、入出力インタフェース等を分析側入出力部34として機能させるものであり、不揮発性メモリ等を血管脈波データ記憶部37および血圧データ記憶部33として機能させるものである。 In the case of a portable information terminal device, a control program stored in a non-volatile memory such as a flash memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a life information input unit 435. At least it is made to function, and an input / output interface or the like is made to function as the analysis side input / output unit 34, and a nonvolatile memory or the like is made to function as the blood vessel pulse wave data storage unit 37 and the blood pressure data storage unit 33.
 生活情報入力部435は、被検体50の食生活や、睡眠時間や、喫煙習慣などの生活情報の入力に用いられるものである。入力された生活情報は、例えば、疾患分析装置430のハードディスクに記憶され、疾患分析部32における疾患リスク分析の際に読み出されて分析に用いられる。 The life information input unit 435 is used to input life information such as the eating habits of the subject 50, sleeping hours, and smoking habits. The input life information is stored in, for example, the hard disk of the disease analysis device 430, and is read out and used for analysis in the disease risk analysis in the disease analysis unit 32.
 上記の構成の疾患リスク分析システム401および疾患分析装置430によれば、上述の第1の実施形態等と比較して、被検体50の生活情報を考慮した疾患リスク分析が行えるため、疾患の分析精度向上を更に図り易くなる。
〔第6の実施形態〕
 次に、本開示の第6の実施形態について図9を参照して説明する。本実施形態の疾患リスク分析システムの基本構成は、第1の実施形態と同様であるが、第1の実施形態とは、疾患分析装置の構成が異なっている。よって、本実施形態においては、図9を用いて疾患分析装置の周辺のみを説明し、その他の構成要素等の説明を繰り返さない。
According to the disease risk analysis system 401 and the disease analysis device 430 having the above-described configuration, the disease risk analysis can be performed in consideration of the life information of the subject 50 as compared with the first embodiment and the like. It becomes easier to improve accuracy.
[Sixth Embodiment]
Next, a sixth embodiment of the present disclosure will be described with reference to FIG. The basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in the present embodiment, only the periphery of the disease analyzer will be described using FIG. 9, and description of other components and the like will not be repeated.
 本実施形態の疾患リスク分析システム501には、図9に示すように、血管モニタ10と、疾患情報管理装置20と、疾患分析装置530と、が主に設けられている。
 疾患分析装置530は、CPU、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置530が、持ち運び可能な被検体50が所有する携帯型情報端末装置である例に適用して説明する。
As shown in FIG. 9, the disease risk analysis system 501 of the present embodiment mainly includes a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 530.
The disease analyzer 530 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In the present embodiment, the disease analysis apparatus 530 will be described as applied to an example of a portable information terminal apparatus owned by a portable subject 50.
 携帯型情報端末装置の場合、フラッシュメモリなどの不揮発性メモリに記憶されている制御プログラムは、CPUを血圧変化情報演算部31、血圧データ演算部36、疾患分析部32および脈拍データ演算部535として少なくとも機能させるものであり、入出力インタフェース等を分析側入出力部34として機能させるものであり、不揮発性メモリ等を血管脈波データ記憶部37および血圧データ記憶部33として機能させるものである。 In the case of a portable information terminal device, a control program stored in a non-volatile memory such as a flash memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a pulse data calculation unit 535. At least it is made to function, and an input / output interface or the like is made to function as the analysis side input / output unit 34, and a nonvolatile memory or the like is made to function as the blood vessel pulse wave data storage unit 37 and the blood pressure data storage unit 33.
 脈拍データ演算部535は、血管脈波データに基づき被検体50の脈拍データを算出するものである。具体的には、血管脈波データ記憶部37に記憶された血管脈波データを呼び出し、呼び出した血管脈波データに基づいて脈拍データを算出する。なお、血管脈波データに基づいて脈拍データを算出する方法としては、公知の方法を用いることができ、特に限定するものではない。算出された脈拍データは、同じ血管脈波データから算出された血圧データと紐付けされて血圧データ記憶部33に記憶される。 The pulse data calculation unit 535 calculates pulse data of the subject 50 based on the blood vessel pulse wave data. Specifically, the vascular pulse wave data stored in the vascular pulse wave data storage unit 37 is called, and the pulse data is calculated based on the called vascular pulse wave data. In addition, as a method for calculating the pulse data based on the blood vessel pulse wave data, a known method can be used and is not particularly limited. The calculated pulse data is associated with blood pressure data calculated from the same vascular pulse wave data and stored in the blood pressure data storage unit 33.
 本実施形態の疾患分析装置530における疾患リスク分析の制御は、第1の実施形態と比較して、血圧データの変化情報を求める際に用いられる血圧データの取得処理が異なっている。 The control of the disease risk analysis in the disease analyzer 530 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
 つまり本実施形態では、血圧データを取得する際に、紐付けされた脈拍データも参照される。例えば、安静時と考えられる範囲に属する脈拍データなどのように同じ範囲に属する脈拍データに紐付けられた複数の血圧データの中から、変化情報の算出に用いられる血圧データを取得する処理が行われる。 That is, in this embodiment, when acquiring blood pressure data, linked pulse data is also referred to. For example, processing for obtaining blood pressure data used for calculating change information from a plurality of blood pressure data linked to pulse data belonging to the same range, such as pulse data belonging to a range considered to be resting, is performed. Is called.
 上記の構成の疾患リスク分析システム501および疾患分析装置330によれば、上述の第1の実施形態等と比較して、被検体50の脈拍データを考慮した疾患リスク分析が行えるため、疾患の分析精度向上を更に図り易くなる。
〔第7の実施形態〕
 次に、本開示の第7の実施形態について図10を参照して説明する。本実施形態の疾患リスク分析システムの基本構成は、第1の実施形態と同様であるが、第1の実施形態とは、疾患分析装置の構成が異なっている。よって、本実施形態においては、図10を用いて疾患分析装置の周辺のみを説明し、その他の構成要素等の説明を繰り返さない。
According to the disease risk analysis system 501 and the disease analysis device 330 configured as described above, disease risk analysis can be performed in consideration of the pulse data of the subject 50 as compared with the first embodiment described above. It becomes easier to improve accuracy.
[Seventh Embodiment]
Next, a seventh embodiment of the present disclosure will be described with reference to FIG. The basic configuration of the disease risk analysis system of this embodiment is the same as that of the first embodiment, but the configuration of the disease analysis device is different from that of the first embodiment. Therefore, in this embodiment, only the periphery of the disease analyzer will be described with reference to FIG. 10, and description of other components will not be repeated.
 本実施形態の疾患リスク分析システム601には、血管モニタ10と、疾患情報管理装置20と、疾患分析装置630と、が主に設けられている。
 疾患分析装置630は、CPU、ROM、RAM、ハードディスク、入出力インタフェース等を有するコンピュータシステムである。本実施形態では、疾患分析装置630が、持ち運び可能な被検体50が所有する携帯型情報端末装置である例に適用して説明する。
The disease risk analysis system 601 of the present embodiment is mainly provided with a blood vessel monitor 10, a disease information management device 20, and a disease analysis device 630.
The disease analyzer 630 is a computer system having a CPU, ROM, RAM, hard disk, input / output interface, and the like. In this embodiment, the disease analysis apparatus 630 will be described as applied to an example in which the portable information terminal apparatus owned by the portable subject 50 is used.
 携帯型情報端末装置の場合、フラッシュメモリなどの不揮発性メモリに記憶されている制御プログラムは、CPUを血圧変化情報演算部31、血圧データ演算部36、疾患分析部32および血流データ演算部635として少なくとも機能させるものであり、入出力インタフェース等を分析側入出力部34として機能させるものであり、不揮発性メモリ等を血管脈波データ記憶部37および血圧データ記憶部33として機能させるものである。 In the case of a portable information terminal device, a control program stored in a non-volatile memory such as a flash memory uses a CPU as a blood pressure change information calculation unit 31, a blood pressure data calculation unit 36, a disease analysis unit 32, and a blood flow data calculation unit 635. At least functions as an input / output interface as an analysis input / output unit 34, and functions as a non-volatile memory as a vascular pulse wave data storage unit 37 and a blood pressure data storage unit 33. .
 血流データ演算部635は、血管脈波データに基づき被検体50の血流データを算出するものである。具体的には、血管脈波データ記憶部37に記憶された血管脈波データを呼び出し、呼び出した血管脈波データに基づいて血流データを算出する。なお、血管脈波データに基づいて血流データを算出する方法としては、公知の方法を用いることができ、特に限定するものではない。算出された血流データは、同じ血管脈波データから算出された血圧データと紐付けされて血圧データ記憶部33に記憶される。 The blood flow data calculation unit 635 calculates blood flow data of the subject 50 based on the blood vessel pulse wave data. Specifically, blood vessel pulse wave data stored in the blood vessel pulse wave data storage unit 37 is called, and blood flow data is calculated based on the called blood vessel pulse wave data. In addition, as a method of calculating blood flow data based on the blood vessel pulse wave data, a known method can be used and is not particularly limited. The calculated blood flow data is associated with blood pressure data calculated from the same vascular pulse wave data and stored in the blood pressure data storage unit 33.
 本実施形態の疾患分析装置630における疾患リスク分析の制御は、第1の実施形態と比較して、血圧データの変化情報を求める際に用いられる血圧データの取得処理が異なっている。 The control of the disease risk analysis in the disease analyzer 630 of the present embodiment is different from the first embodiment in the blood pressure data acquisition process used when obtaining change information of the blood pressure data.
 つまり本実施形態では、血圧データを取得する際に、紐付けされた血流データも参照される。例えば、安静時と考えられる範囲に属する血流データなどのように同じ範囲に属する血流データに紐付けられた複数の血圧データの中から、変化情報の算出に用いられる血圧データを取得する処理が行われる。 That is, in the present embodiment, when blood pressure data is acquired, linked blood flow data is also referred to. For example, processing for obtaining blood pressure data used for calculating change information from a plurality of blood pressure data linked to blood flow data belonging to the same range, such as blood flow data belonging to a range considered to be resting Is done.
 上記の構成の疾患リスク分析システム601および疾患分析装置330によれば、上述の第1の実施形態等と比較して、被検体50の血流データを考慮した疾患リスク分析が行えるため、疾患の分析精度向上を更に図り易くなる。
図11に、上述した第1~7実施形態における疾患情報管理装置20及び疾患分析装置30,130,230,330,430,530及び630に共通する電気的構成を示す。コンピュータシステム2は、CPU3と、ROM4と、RAM5と、ハードディスク6と、入力インタフェース7等とを含む。
According to the disease risk analysis system 601 and the disease analysis device 330 configured as described above, the disease risk analysis can be performed in consideration of the blood flow data of the subject 50 as compared with the first embodiment described above. It becomes easier to improve the analysis accuracy.
FIG. 11 shows an electrical configuration common to the disease information management apparatus 20 and the disease analysis apparatuses 30, 130, 230, 330, 430, 530, and 630 in the first to seventh embodiments described above. The computer system 2 includes a CPU 3, a ROM 4, a RAM 5, a hard disk 6, an input interface 7, and the like.
 上記第1~7の実施形態の説明では、制御プログラムがフラッシュメモリに格納されている場合について説明したが、プログラムを格納する非一時的なコンピュータ可読媒体は、これに限らない。非一時的なコンピュータ可読媒体は、例えば、フレキシブルディスク、磁気テープ、ハードディスクなどの磁気記録媒体、光磁気ディスクなどの光磁気記録媒体、CD-ROM(Compact Disc Read Only Memory)などの光学記録媒体、ROM(Read Only Memory),フラッシュメモリ及びRAM(Random Access Memory)などの半導体メモリを含むが、これに限らない。 In the above description of the first to seventh embodiments, the case where the control program is stored in the flash memory has been described, but the non-transitory computer-readable medium for storing the program is not limited to this. Non-transitory computer-readable media include, for example, magnetic recording media such as flexible disks, magnetic tapes, and hard disks, magneto-optical recording media such as magneto-optical disks, optical recording media such as CD-ROM (Compact Read Only Memory), Including, but not limited to, semiconductor memories such as ROM (Read Only Memory), flash memory, and RAM (Random Access Memory).
 なお、本開示の技術範囲は上記実施形態に限定されるものではなく、本開示の趣旨を逸脱しない範囲において種々の変更を加えることが可能である。例えば、本開示を上記の実施形態に適用したものに限られることなく、これらの実施形態を適宜組み合わせた実施形態に適用してもよく、特に限定するものではない。  Note that the technical scope of the present disclosure is not limited to the above embodiment, and various modifications can be made without departing from the spirit of the present disclosure. For example, the present disclosure is not limited to those applied to the above-described embodiments, and may be applied to embodiments in which these embodiments are appropriately combined, and is not particularly limited.

Claims (21)

  1.  疾患分析装置であって、
     血管関連データ計測部において連続的に測定された被検体の血管関連データを記憶する血管関連データ記憶部と、
     前記血管関連データに基づき、血圧データを算出する血圧データ演算部と、
     前記血圧データ演算部において算出された前記血圧データを記憶する血圧データ記憶部と、
     少なくとも前記血圧データ記憶部に記憶された血圧データから、任意の少なくとも二つの血圧データを取得し、取得した前記少なくとも二つの血圧データの変化量に関する情報である変化情報を算出する血圧変化情報演算部と、
     前記変化情報と疾患リスク情報とが関連付けされた血圧疾患データベースを参照し、前記血圧変化情報演算部により算出された前記変化情報に関連付けされた前記疾患リスク情報を取得して疾患リスクを分析する疾患分析部と、を備えた、疾患分析装置。
    A disease analyzer,
    A blood vessel related data storage unit for storing blood vessel related data of the subject continuously measured in the blood vessel related data measurement unit;
    A blood pressure data calculation unit for calculating blood pressure data based on the blood vessel related data;
    A blood pressure data storage unit for storing the blood pressure data calculated in the blood pressure data calculation unit;
    A blood pressure change information calculation unit that acquires any at least two blood pressure data from at least the blood pressure data stored in the blood pressure data storage unit, and calculates change information that is information regarding a change amount of the acquired at least two blood pressure data When,
    A disease whose disease risk is analyzed by referring to a blood pressure disease database in which the change information and disease risk information are associated, and acquiring the disease risk information associated with the change information calculated by the blood pressure change information calculation unit A disease analysis apparatus comprising: an analysis unit;
  2.  前記血圧データ記憶部には、時間計測部により測定された時間情報が入力され、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記時間情報とを紐付けして記憶する、請求項1に記載の疾患分析装置。
    The blood pressure data storage unit receives time information measured by a time measurement unit,
    The disease analysis apparatus according to claim 1, wherein the blood pressure data storage unit associates and stores the blood pressure data and the time information when the blood pressure data is measured.
  3.  前記血圧データ記憶部には、温度計測部により測定された前記被検体の温度情報が入力され、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記温度情報とを紐付けして記憶する、請求項1に記載の疾患分析装置。
    The blood pressure data storage unit receives temperature information of the subject measured by a temperature measurement unit,
    The disease analysis apparatus according to claim 1, wherein the blood pressure data storage unit associates and stores the blood pressure data and the temperature information when the blood pressure data is measured.
  4.  前記血圧データ記憶部には、前記温度情報を用いて判定部により判定された前記被検体の活動状態情報が入力され、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記活動状態情報とを紐付けして記憶する、請求項3に記載の疾患分析装置。
    The blood pressure data storage unit receives the activity state information of the subject determined by the determination unit using the temperature information,
    The disease analysis apparatus according to claim 3, wherein the blood pressure data storage unit associates and stores the blood pressure data and the activity state information when the blood pressure data is measured.
  5.  前記血圧データ記憶部には、加速度計測部において測定された被検体の加速度情報が入力され、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記加速度情報とを紐付けして記憶する、請求項1に記載の疾患分析装置。
    The blood pressure data storage unit receives acceleration information of the subject measured by the acceleration measurement unit,
    The disease analysis apparatus according to claim 1, wherein the blood pressure data storage unit associates and stores the blood pressure data and the acceleration information when the blood pressure data is measured.
  6.  前記血圧データ記憶部には、前記加速度情報を用いて判定部により判定された前記被検体の活動状態情報が入力され、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記活動状態情報とを紐付けして記憶する、請求項5に記載の疾患分析装置。
    The blood pressure data storage unit receives the activity state information of the subject determined by the determination unit using the acceleration information,
    The disease analysis apparatus according to claim 5, wherein the blood pressure data storage unit associates and stores the blood pressure data and the activity state information when the blood pressure data is measured.
  7.  前記血圧変化情報演算部は、前記時間情報に基づいて、前記時間情報に紐付けされた前記血圧データを取得することにより、前記少なくとも二つの血圧データを取得する請求項2に記載の疾患分析装置。 The disease analysis apparatus according to claim 2, wherein the blood pressure change information calculation unit acquires the at least two blood pressure data by acquiring the blood pressure data associated with the time information based on the time information. .
  8.  前記血圧変化情報演算部は、前記温度情報に基づいて、前記温度情報に紐付けされた前記血圧データを取得することにより、前記少なくとも二つの血圧データを取得する、請求項3に記載の疾患分析装置。 The disease analysis according to claim 3, wherein the blood pressure change information calculation unit acquires the at least two blood pressure data by acquiring the blood pressure data associated with the temperature information based on the temperature information. apparatus.
  9.  前記血圧変換情報演算部は、前記加速度情報に基づいて、前記加速度情報に紐付けされた前記血圧データを取得することにより、前記少なくとも二つの血圧データを取得する、請求項5に記載の疾患分析装置。 The disease analysis according to claim 5, wherein the blood pressure conversion information calculation unit acquires the at least two blood pressure data by acquiring the blood pressure data associated with the acceleration information based on the acceleration information. apparatus.
  10.  前記血圧変換情報演算部は、前記活動状態情報に基づいて、前記活動状態情報に紐付けされた前記血圧データを取得することにより、前記少なくとも二つの血圧データを取得する、請求項4に記載の疾患分析装置。 5. The blood pressure conversion information calculation unit according to claim 4, wherein the blood pressure conversion information calculation unit obtains the at least two blood pressure data by obtaining the blood pressure data associated with the activity state information based on the activity state information. Disease analyzer.
  11.  前記疾患分析装置は、さらに、前記血管関連データに基づき、脈拍データを算出する脈拍データ演算部を備え、
     前記血圧データ記憶部には、前記脈拍データ演算部により算出された前記脈拍データが入力され、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記脈拍データとを紐付けして記憶する、請求項1に記載の疾患分析装
    置。
    The disease analyzer further includes a pulse data calculation unit that calculates pulse data based on the blood vessel related data,
    The pulse data calculated by the pulse data calculation unit is input to the blood pressure data storage unit,
    The disease analysis apparatus according to claim 1, wherein the blood pressure data storage unit associates and stores the blood pressure data and the pulse data when the blood pressure data is measured.
  12.  前記疾患分析装置は、さらに、前記血管関連データに基づき、血流データを算出する血流データ演算部を備え、
     前記血圧データ記憶部には、前記血流データ演算部により算出された前記血流データが入力され、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記血流データとを紐付けして記憶する、請求項1に記載の疾患分析装置。
    The disease analyzer further includes a blood flow data calculation unit that calculates blood flow data based on the blood vessel related data,
    The blood flow data calculated by the blood flow data calculation unit is input to the blood pressure data storage unit,
    The disease analysis apparatus according to claim 1, wherein the blood pressure data storage unit associates and stores the blood pressure data and the blood flow data when the blood pressure data is measured.
  13.  疾患リスク分析システムであって、
     被検体の血管関連データを計測する血管関連データ計測部を備えた生体情報取得装置と、
     少なくとも二つの血圧データの変化量に関する情報である変化情報と疾患リスク情報とが関連付けされた血圧疾患データベースを備えた疾患情報管理装置と、
     前記血管関連データ計測部において連続的に測定された前記被検体の前記血管関連データを記憶する血管関連データ記憶部と、
     前記血管関連データに基づき、前記血圧データを算出する血圧データ演算部と、
     前記血圧データ演算部において算出された前記血圧データ記憶部と、
     前記血圧データ記憶部に記憶された前記血圧データから任意の少なくとも二つの血圧データを取得し、取得した前記少なくとも二つの血圧データに関する前記変化情報を算出する血圧変化情報演算部と、
     前記血圧疾患データベースを参照し、前記変化情報に関連付けされた前記疾患リスク情報を取得して疾患リスクを分析する疾患分析部と、を備えた、疾患分析装置と、を有する、疾患リスク分析システム。
    A disease risk analysis system,
    A biological information acquisition device including a blood vessel related data measuring unit for measuring blood vessel related data of a subject;
    A disease information management device comprising a blood pressure disease database in which change information that is information related to the amount of change in at least two blood pressure data and disease risk information are associated;
    A blood vessel related data storage unit that stores the blood vessel related data of the subject continuously measured in the blood vessel related data measurement unit;
    A blood pressure data calculation unit for calculating the blood pressure data based on the blood vessel related data;
    The blood pressure data storage unit calculated in the blood pressure data calculation unit;
    A blood pressure change information calculation unit that acquires any at least two blood pressure data from the blood pressure data stored in the blood pressure data storage unit, and calculates the change information related to the acquired at least two blood pressure data;
    A disease risk analysis system comprising: a disease analysis device comprising: a disease analysis unit that refers to the blood pressure disease database and acquires the disease risk information associated with the change information and analyzes the disease risk.
  14.  生体情報取得装置が、前記被検体の温度情報を測定する温度計測部を備え、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記時間情報とを紐付けして記憶する、請求項13に記載の疾患分析システム。
    The biological information acquisition apparatus includes a temperature measurement unit that measures temperature information of the subject,
    The disease analysis system according to claim 13, wherein the blood pressure data storage unit stores the blood pressure data in association with the time information when the blood pressure data is measured.
  15.  生体情報取得装置が、前記被検体の加速度情報を測定する加速度計測部を備え、
     前記血圧データ記憶部は、前記血圧データと、当該血圧データを測定した際の前記加速度情報とを紐付けして記憶する、請求項14に記載の疾患分析システム。
    The biological information acquisition apparatus includes an acceleration measurement unit that measures acceleration information of the subject,
    The disease analysis system according to claim 14, wherein the blood pressure data storage unit associates and stores the blood pressure data and the acceleration information when the blood pressure data is measured.
  16.  前記疾患分析装置が前記被検体の保有する携帯端末装置である、請求項13に記載の疾患リスク分析システム。 The disease risk analysis system according to claim 13, wherein the disease analysis device is a portable terminal device held by the subject.
  17.  前記携帯端末装置が前記被検体の身体情報を入力する身体情報入力部を備える、請求項16記載の疾患リスク分析システム。 The disease risk analysis system according to claim 16, wherein the portable terminal device includes a body information input unit for inputting body information of the subject.
  18.  前記携帯端末装置が前記被検体の生活習慣を入力する生活習慣入力部を備える、請求項16に記載の疾患リスク分析システム。 The disease risk analysis system according to claim 16, wherein the mobile terminal device includes a lifestyle input unit that inputs a lifestyle of the subject.
  19.  疾患情報管理装置が、前記被検体に関する管理ID、パスワード、疾患分析情報に関する属性データを格納する個人情報データベースをさらに備える、請求項13に記載の疾患リスク分析システム。 The disease risk analysis system according to claim 13, wherein the disease information management device further comprises a personal information database that stores a management ID, a password, and attribute data related to disease analysis information related to the subject.
  20.  前記疾患分析装置が、携帯型情報端末装置である、請求項13に記載の疾患リスク分析システム。 The disease risk analysis system according to claim 13, wherein the disease analysis device is a portable information terminal device.
  21.  非一時的コンピュータ可読媒体であって、
     コンピュータに、
     血管関連データ計測部において異なる時間に測定された少なくとも二つの血管関連データに基づく血圧データを取得し、取得した前記少なくとも二つの血圧データの変化量に関する情報である変化情報を算出する血圧変化情報演算機能と、
     前記変化情報と疾患リスク情報とが関連付けされた血圧疾患データベースを参照し、前記変化情報に関連付けされた前記疾患リスク情報を取得して疾患リスクを分析する疾患分析機能と、を実現させる疾患分析プログラムを格納した非一時的コンピュータ可読媒体。
    A non-transitory computer readable medium comprising:
    On the computer,
    Blood pressure change information calculation for obtaining blood pressure data based on at least two blood vessel related data measured at different times in the blood vessel related data measuring unit, and calculating change information that is information regarding a change amount of the acquired at least two blood pressure data Function and
    A disease analysis program that realizes a disease analysis function that refers to a blood pressure disease database in which the change information and disease risk information are associated, acquires the disease risk information associated with the change information, and analyzes the disease risk A non-transitory computer readable medium having stored therein.
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Citations (3)

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Publication number Priority date Publication date Assignee Title
JP2004261452A (en) * 2003-03-03 2004-09-24 ▲苅▼尾 七臣 Hemodynamometer and risk analyzing program for cardiovascular system disease
JP2006204320A (en) * 2005-01-25 2006-08-10 Nippon Telegr & Teleph Corp <Ntt> Blood pressure measuring apparatus
JP2009213767A (en) * 2008-03-12 2009-09-24 Omron Healthcare Co Ltd Blood pressure information measuring apparatus

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004261452A (en) * 2003-03-03 2004-09-24 ▲苅▼尾 七臣 Hemodynamometer and risk analyzing program for cardiovascular system disease
JP2006204320A (en) * 2005-01-25 2006-08-10 Nippon Telegr & Teleph Corp <Ntt> Blood pressure measuring apparatus
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