WO2012074039A1 - 医用画像処理装置 - Google Patents
医用画像処理装置 Download PDFInfo
- Publication number
- WO2012074039A1 WO2012074039A1 PCT/JP2011/077761 JP2011077761W WO2012074039A1 WO 2012074039 A1 WO2012074039 A1 WO 2012074039A1 JP 2011077761 W JP2011077761 W JP 2011077761W WO 2012074039 A1 WO2012074039 A1 WO 2012074039A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- value
- image
- signal value
- brain
- slice
- Prior art date
Links
- 238000012545 processing Methods 0.000 title claims abstract description 124
- 210000004556 brain Anatomy 0.000 claims abstract description 165
- 238000000034 method Methods 0.000 claims abstract description 111
- 230000008569 process Effects 0.000 claims abstract description 81
- 230000001629 suppression Effects 0.000 claims description 60
- 210000003625 skull Anatomy 0.000 claims description 42
- 238000009826 distribution Methods 0.000 claims description 19
- 238000005259 measurement Methods 0.000 claims description 19
- 230000002093 peripheral effect Effects 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 230000008859 change Effects 0.000 claims description 8
- 230000002060 circadian Effects 0.000 claims description 7
- 238000012886 linear function Methods 0.000 claims description 4
- 238000000926 separation method Methods 0.000 abstract description 22
- 210000004884 grey matter Anatomy 0.000 description 56
- 210000004885 white matter Anatomy 0.000 description 55
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 37
- 201000010099 disease Diseases 0.000 description 36
- 238000002595 magnetic resonance imaging Methods 0.000 description 29
- 210000001519 tissue Anatomy 0.000 description 25
- 238000003745 diagnosis Methods 0.000 description 13
- 230000009466 transformation Effects 0.000 description 13
- 238000010586 diagram Methods 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 238000012360 testing method Methods 0.000 description 9
- 238000004458 analytical method Methods 0.000 description 8
- 238000007781 pre-processing Methods 0.000 description 8
- 208000024827 Alzheimer disease Diseases 0.000 description 7
- 238000004422 calculation algorithm Methods 0.000 description 7
- 238000012937 correction Methods 0.000 description 7
- 241000287513 Anhingidae Species 0.000 description 6
- 206010003694 Atrophy Diseases 0.000 description 5
- 230000037444 atrophy Effects 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- 238000009499 grossing Methods 0.000 description 5
- 238000000605 extraction Methods 0.000 description 4
- 238000002600 positron emission tomography Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000003672 processing method Methods 0.000 description 3
- PXFBZOLANLWPMH-UHFFFAOYSA-N 16-Epiaffinine Natural products C1C(C2=CC=CC=C2N2)=C2C(=O)CC2C(=CC)CN(C)C1C2CO PXFBZOLANLWPMH-UHFFFAOYSA-N 0.000 description 2
- 206010012289 Dementia Diseases 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 230000017531 blood circulation Effects 0.000 description 2
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 238000013507 mapping Methods 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 208000024806 Brain atrophy Diseases 0.000 description 1
- 208000014644 Brain disease Diseases 0.000 description 1
- 238000012952 Resampling Methods 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 206010072731 White matter lesion Diseases 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000019771 cognition Effects 0.000 description 1
- 238000002591 computed tomography Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000012812 general test Methods 0.000 description 1
- 238000003706 image smoothing Methods 0.000 description 1
- 238000012905 input function Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000013425 morphometry Methods 0.000 description 1
- 210000004126 nerve fiber Anatomy 0.000 description 1
- 210000002569 neuron Anatomy 0.000 description 1
- 238000009206 nuclear medicine Methods 0.000 description 1
- 238000011158 quantitative evaluation Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000012353 t test Methods 0.000 description 1
- 238000003325 tomography Methods 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06T—IMAGE DATA PROCESSING OR GENERATION, IN GENERAL
- G06T7/00—Image analysis
- G06T7/0002—Inspection of images, e.g. flaw detection
- G06T7/0012—Biomedical image inspection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/05—Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves
- A61B5/055—Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves involving electronic [EMR] or nuclear [NMR] magnetic resonance, e.g. magnetic resonance imaging
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06T—IMAGE DATA PROCESSING OR GENERATION, IN GENERAL
- G06T5/00—Image enhancement or restoration
- G06T5/90—Dynamic range modification of images or parts thereof
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06T—IMAGE DATA PROCESSING OR GENERATION, IN GENERAL
- G06T7/00—Image analysis
- G06T7/30—Determination of transform parameters for the alignment of images, i.e. image registration
- G06T7/33—Determination of transform parameters for the alignment of images, i.e. image registration using feature-based methods
- G06T7/337—Determination of transform parameters for the alignment of images, i.e. image registration using feature-based methods involving reference images or patches
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06T—IMAGE DATA PROCESSING OR GENERATION, IN GENERAL
- G06T7/00—Image analysis
- G06T7/60—Analysis of geometric attributes
- G06T7/62—Analysis of geometric attributes of area, perimeter, diameter or volume
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06T—IMAGE DATA PROCESSING OR GENERATION, IN GENERAL
- G06T2207/00—Indexing scheme for image analysis or image enhancement
- G06T2207/20—Special algorithmic details
- G06T2207/20112—Image segmentation details
- G06T2207/20128—Atlas-based segmentation
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06T—IMAGE DATA PROCESSING OR GENERATION, IN GENERAL
- G06T2207/00—Indexing scheme for image analysis or image enhancement
- G06T2207/30—Subject of image; Context of image processing
- G06T2207/30004—Biomedical image processing
- G06T2207/30016—Brain
Definitions
- the present invention relates to a technique for performing diagnosis support for a brain disease by performing image processing on a brain image obtained by MRI (Magnetic Resonance Imaging), and in particular, a brain image obtained by MRI or the like in a state suitable for diagnosis support. It relates to processing technology.
- MRI Magnetic Resonance Imaging
- SPECT Single Photon Emission
- Information on the state of the brain can be acquired by nuclear medicine examination such as computed tomography (PET) and PET (positron emission tomography), CT (computerized tomography) and MRI.
- a decrease in blood flow or metabolism in a local region of the brain can be tested by comparing with SPECT or PET images.
- the volume of a specific part can be obtained from an MRI image, and the relative size can be compared to determine the presence or absence of an abnormality.
- a brain image obtained by imaging the head of a subject is subjected to image processing in units of voxels that are three-dimensional pixels. Based Morphometry) is known (for example, see Patent Document 1).
- This VBM method is an effective evaluation method for identifying Alzheimer's disease, and it has been reported that there was 87.8% diagnostic ability in distinguishing between healthy subjects and Alzheimer's disease (see Non-Patent Document 1). .
- an object of the present invention is to provide a medical image processing apparatus that can determine the state of an acquired brain image and adjust it to a brain image suitable for tissue separation processing.
- target slice selection means for selecting a slice image to be processed as a target slice from a brain image composed of a plurality of slice images, and brain parenchyma pixels
- Brain parenchyma measurement means for performing measurement processing of the brain parenchymal effective maximum value which is the effective maximum value of the signal value
- brain image measurement means for performing measurement processing of the effective maximum value of the signal value of the pixel of the entire brain image, and the skull peripheral region
- the cranial measurement means that measures and processes the average of the signal values of the pixels that become the peak as the peak average value of the circadian revolution, the effective maximum value of the measured brain parenchyma, the effective maximum value of the entire brain image, the peak average value of the circadian circumference
- a suppression processing determination unit that determines whether a high signal value suppression process is necessary or not, and executes a high signal value suppression process on the brain image when the suppression process determination unit determines that the high signal value suppression process is necessary.
- the target slice of the brain image is selected, and for the selected slice, the effective maximum value of the signal value of the pixel of the brain parenchyma, the effective maximum value of the signal value of the pixel of the entire brain image, Measure the peak average value of the circadian circumference, which is the average of the signal values of the pixels that become the peak of the region around the skull, and if necessary, perform high signal value suppression processing on the brain image
- the state of the acquired brain image can be determined and adjusted to a brain image suitable for tissue separation processing.
- the suppression processing determination means determines whether or not the peak average value of the circadian circumference is higher than the brain parenchyma effective maximum value by a certain percentage. Performing a skull region determination, which is a determination, and an entire image determination, which is a determination as to whether a signal value of the entire image is higher than the brain parenchyma effective maximum value by a certain percentage, and either the skull region determination or the entire image determination When one of the conditions is satisfied, it is determined that high signal value suppression processing is necessary.
- the second aspect of the present invention it is determined whether or not the peak average value in the region around the skull and the signal value of the entire image are higher than the brain parenchyma effective maximum value by a certain percentage, the peak average value in the region around the skull, the entire image
- the high signal value suppression processing is necessary, so if the signal value in the region around the skull is significantly higher than the brain parenchyma, In any case where the signal value in the region other than the brain parenchyma is significantly higher than the brain parenchyma, it is possible to accurately determine that the high signal value suppression processing is necessary.
- the target slice selecting means sets a predetermined line segment in the image for each slice image, Among the pixels located on the line segment and having a signal value equal to or greater than a predetermined value, the length between the farthest pixels is obtained, and the length between the pixels is a predetermined value compared to the longest of all slice images.
- a slice image having a ratio or higher is selected as a target slice.
- a slice image in which pixels having a signal value equal to or greater than a predetermined value are equal to or greater than a predetermined ratio in all slice images is selected as a target slice.
- the brain parenchyma measuring means determines the center of the brain for each selected target slice. Set a predetermined number of line segments to pass through, divide the signal value distribution of the pixels on the line segment into a predetermined number of areas for each line segment, and set the central predetermined number of areas as the brain parenchymal area, the signal value in the brain parenchymal area The maximum value of the signal obtained by removing the upper predetermined pixels is obtained as the effective maximum value of the brain parenchyma.
- the signal value distribution for each of a plurality of line segments passing through the central part of the brain is divided into a predetermined number of regions, and the central predetermined number of regions are divided into the brain. Since the histogram of the signal value in the brain parenchyma area is obtained as the real area, and the maximum value of the signal obtained by removing the upper predetermined pixels is obtained as the effective maximum value of the brain parenchyma, the brain that is a value representative of the brain parenchyma It is possible to accurately determine the actual effective maximum value.
- the brain image measurement means obtains a histogram of signal values of pixels of the entire target slice, The maximum value of the signal from which the predetermined pixels are removed is obtained as the effective maximum value of the entire image.
- the histogram of the signal values of the pixels of the entire target slice is obtained, and the maximum value of the signal from which the upper predetermined pixels are removed is obtained as the effective maximum value of the entire image. It is possible to accurately obtain the effective maximum value of the entire image, which is a value representing the entire image.
- the skull measurement means passes through the center of the brain for each selected target slice.
- Set a predetermined number of line segments divide the signal value distribution of the pixels on the line segment into a predetermined number of areas for each line segment, and use the predetermined number of areas at both ends as the skull peripheral area, and the maximum signal value in the skull peripheral area
- the average value of all the line segments of all the target slices is obtained as the peak average value of the circadian gyrus.
- the signal value distribution for each of a plurality of line segments passing through the center of the brain is divided into a predetermined number of regions, and the predetermined number of regions at both ends are used as the skull peripheral region. Since the average value of all signal segments of all target slices of the maximum signal value in the skull peripheral region is obtained as the peak average value of the skull periphery, the peak of the skull periphery that is a value representative of the skull peripheral region The average value can be obtained accurately.
- the high signal value suppression processing means For a pixel having a signal value equal to or greater than the predetermined value without changing the signal value, relatively high signal value suppression processing is realized by executing processing for setting the signal value to a predetermined value.
- the signal value is not changed, and for a pixel whose signal value is equal to or greater than a predetermined value, a process of setting the signal value to a predetermined value is executed. As a result, the high signal value of the input image can be suppressed.
- the high signal value suppression processing means For a pixel whose signal value is not less than the predetermined value without changing the signal value, a process for converting the signal value to be smaller than the original value is executed, thereby realizing a relatively high signal value suppression process. It is characterized by being.
- the signal value is not changed for a pixel whose signal value is less than the predetermined value, and the signal value is smaller than the original value for a pixel whose signal value is the predetermined value or more. Since the conversion process is executed as described above, the high signal value of the input image can be suppressed.
- the high signal value suppression processing means does not change a signal value of a pixel having a signal value less than a predetermined value.
- relatively high signal value suppression processing is realized by executing processing for converting the signal value by a linear function having a slope of zero or more and smaller than 1. It is characterized by being.
- the signal value is not changed for a pixel whose signal value is less than a predetermined value, and the signal value of the pixel whose signal value is greater than or equal to the predetermined value is 1 or more with a slope of zero or more. Since the process of converting with a small linear function is executed, the high signal value of the input image can be suppressed. Further, the result of the tissue separation process becomes a natural image.
- the present invention it is possible to determine the state of the acquired brain image and adjust it to a brain image suitable for tissue separation processing.
- FIG. 1 is a block diagram showing an outline of a medical image processing apparatus according to an embodiment of the present invention.
- the flowchart which shows the basic process sequence of the medical image processing method by this embodiment
- the flowchart which shows the pre-processing procedure of the medical image processing method by this embodiment
- Conceptual diagram showing brain slice images and voxel characteristics
- Flow chart showing details of preparation process
- the figure which shows the mode of selection processing of the object slice Diagram showing the distribution of signal values in the brain parenchyma and the area around the skull
- Conceptual image showing gray matter, white matter age template
- Conceptual image showing gray matter, white matter gender template
- Conceptual diagram schematically showing the features of spatial standardization
- Conceptual diagram showing the characteristics of nonlinear transformation
- Conceptual diagram showing the results of spatial standardization and smoothing
- Conceptual diagram showing the characteristics of the comparison test for each voxe
- FIG. 1 is a block diagram showing a medical image processing apparatus according to an embodiment of the present invention.
- the medical image processing apparatus according to the present embodiment illustrated in FIG. 1 includes a user interface 10, an image / statistic processing unit 20, and a database unit 30.
- the user interface 10 includes an image input function 12 for inputting an MRI image as an input image, and a result display function 14 for displaying a result processed by the image / statistic processing unit 20.
- An image processing function 22 for processing an MRI image input from the user interface 10, a statistical processing function 24 for performing various statistical calculations, and a high signal value for determining whether or not high signal value suppression is necessary or unnecessary for the input image.
- a suppression necessity / unnecessity determination function 26 is provided.
- the database unit 30 stores a white matter brain image template 32, a gray matter brain image template 34, a healthy subject image database 36, a disease-specific ROI 38, and the like used for processing to be described later by the image / statistical processing unit 20.
- FIG. 2 is a flowchart showing an outline of processing of the medical image processing apparatus according to this embodiment
- FIG. 3 is a flowchart showing a pre-processing procedure of the medical image processing method according to this embodiment.
- FIG. 2 first, when an MRI brain image of a subject is input, predetermined processing is performed on the brain image to determine whether high signal value suppression processing should be performed, and according to the determination result. High signal value suppression processing is performed (S1). In S1, depending on the determination result, the high signal value suppression process may not be performed.
- S1 is a feature of the present invention. Details of the processing in S1 will be described later.
- the brain image after the high signal value suppression process (or the input MRI brain image when the high signal value suppression process is not performed) is aligned to correct spatial deviation (S2). Subsequently, a gray matter image in which the gray matter is extracted together with the white matter image in which the white matter has been extracted by the tissue separation process is created from the brain image after the alignment (S3).
- each of the processes of S1 to S7 can be implemented by a program in the image / statistical processing unit 20 formed of a computer, and white matter and gray-white by the processes of S11 to S14 described below. Quality templates can be created by the program as well.
- pre-processing for creating a template used for spatial standardization of S4 is performed in S11 to S14 of FIG.
- T1-weighted MRI brain images are input from as many healthy subjects as possible.
- Pre-processing is performed for MRI brain images acquired from each subject. Specifically, as shown in FIG. 4, an image of a slice image obtained by cutting out the entire brain and a part of the brain, for example, 100 to 200 images taken in a slice of a predetermined thickness so as to include the entire brain of the subject.
- the T1-weighted MRI image is input.
- the resampling of the slice image is performed so that the length of each side of the voxel in each slice image becomes equal in advance.
- a voxel is a coordinate unit of an image having “thickness” and corresponds to a pixel in a two-dimensional image.
- a preparation process is performed (S11).
- the preparation process determines whether the high signal value suppression process should be performed on the input image so that the tissue separation process is accurately performed. High signal value suppression processing is performed.
- FIG. 5 is a flowchart showing details of the preparation process.
- a process of selecting a slice image used as a determination target from the input image as a target slice is performed (S21).
- FIG. 6 shows how the target slice is selected.
- As the target slice it is desirable to select a portion that does not include a high signal value other than the region around the skull and the brain parenchyma.
- a predetermined line segment is set in the image, and the length between the farthest pixels among the pixels located on the line segment and having a signal value equal to or greater than a predetermined value is set.
- a line segment to be set in the image a line segment passing through most of the imaged region around the skull and the brain parenchyma is set.
- a diagonal line of the image may be used as the line segment.
- the predetermined value to be compared with the signal value can be appropriately set. For example, it can be a value obtained by multiplying the average of the signal values of the entire image by a predetermined constant.
- Pixels with a signal value greater than or equal to a predetermined value indicate the region around the cranium, and among pixels with a signal value equal to or greater than a predetermined value, the distance between the farthest pixels indicates the length of overlap between the line segment and the head. ing.
- the target slice it is desirable to select a slice image that does not include a high signal value other than the peripheral region of the skull and the brain parenchyma, but that portion is 80 to 95% of the maximum portion of the head. It exists in the position that becomes the length. Therefore, in the present embodiment, a slice image in which the length between the pixels is maximized is specified, and a slice image in which the length between the pixels is 80 to 95% of the specified slice image is targeted. Select as a slice.
- the measurement process of the effective maximum value of the brain parenchyma is performed (S22).
- the signal value distribution of the brain parenchyma is acquired.
- the signal value distribution of the region around the skull is also acquired at the same time.
- FIG. 7 shows the signal value distribution in the brain parenchyma and the region around the skull.
- the signal value of the pixel on a line segment is plotted about each line segment. Further, the signal value distribution is divided into a predetermined number of regions according to the line segment, and the central predetermined number of regions is defined as the brain parenchymal region, and the predetermined number of regions at both ends are defined as the skull peripheral region. In this embodiment, as shown in the signal value distribution on the right side of FIG. 7A, the area is divided into 10 areas, the central 4 areas are the brain parenchyma area, and each area on both ends (2 areas in total) is the skull. The surrounding area. A and B in the signal value distribution correspond to A and B on the brain image shown on the left side of FIG.
- FIG. 8A shows the state of measurement processing of the effective maximum value of the brain parenchyma. As shown in the histogram at the bottom of FIG. 8A, the value of the portion indicated by the arrow excluding the upper 3% shaded pixels is the brain parenchyma effective maximum value Bmax.
- measurement processing of the effective maximum value of the entire image is performed (S23). Specifically, a histogram of the signal values of the pixels of the entire rectangular target slice is obtained, and the maximum value when a portion affected by the high signal artifact is excluded is obtained as the effective maximum value Imax of the entire image.
- FIG. 8B shows the state of the measurement process of the peak average value of the cranial orbit.
- the average of the signal values of the number of target slices ⁇ 20 is calculated as the peak average value Pave of the cranial circle.
- S25 it is determined whether or not high signal value suppression is necessary (S25). Specifically, when two types of determinations, the skull region determination and the entire image determination, are performed, and if any of these determination conditions is satisfied, it is determined that high signal value suppression is necessary, and neither of the determination conditions is satisfied In addition, it is determined that high signal value suppression is unnecessary.
- the skull region determination is performed to determine whether or not the signal value in the region around the skull is higher than the brain parenchymal region by a certain percentage. Specifically, processing according to the following [Formula 1] is executed.
- the whole image determination is to determine whether or not the signal value of the entire image is higher than the brain parenchyma by a certain percentage. Specifically, processing according to the following [Formula 2] is executed.
- the process proceeds to the high signal value suppression process (S26).
- the high signal value suppression process is not performed and the preparation is performed. The process ends. This is because the high signal values other than the brain parenchyma are not so high as to hinder the tissue separation process when neither the conditions of the skull region determination or the entire image determination are satisfied, and there is no need for high signal value suppression.
- either the skull region determination or the entire image determination may be performed first. If the determination is satisfied first, the high signal value suppression process is performed without determining the other determination condition. Proceed to (S26).
- the high signal value suppression process is a process of suppressing the value of a pixel having a high signal value from pixels of the input image so as not to be relatively high. For this reason, various methods can be used as long as the processing is performed to suppress the value of a pixel having a high signal value so as not to be relatively high as compared to other pixels.
- the signal value is fixed, and for a pixel that is less than a certain fixed value, processing that does not change the signal value is performed. Relatively high signal value suppression processing is realized.
- the signal value s (x, y) at each pixel (x, y) of the input image is converted into the signal value s ′ (x, y). To correct.
- the signal value is converted by a linear function having a slope a larger than zero and smaller than 1, and for a pixel less than a certain fixed value. May execute relatively high signal value suppression processing by executing processing that does not change the signal value. As a result, the rate of change of the signal value above a certain fixed value becomes smaller than the rate of change of the signal value below a certain fixed value, and the value of the pixel having a high signal value can be suppressed so as not to become relatively high. .
- the second method since the signal value above a certain value is gently increased, the result of the tissue separation process becomes a more natural image.
- a signal value s (x, y) at each pixel (x, y) of the input image is obtained as a signal value s by executing processing according to the following [Equation 4]. Correct to '(x, y).
- the high signal value suppression process is realized by the process according to the above [Equation 3] or [Equation 4].
- the signal value is changed to the original value. Any processing that converts the value to be smaller than the value may be used, and it may be realized by using another known method such as gamma correction.
- the process returns to the flowchart of FIG. 3 and the subsequent processes are executed.
- subsequent steps S12 to S14 the image for which high signal value suppression is performed is processed for the corrected image, and the image for which high signal value suppression is not performed is processed for the input image.
- a spatial alignment process is performed (S12). This is equivalent to correcting the spatial position and angle by linear transformation (affine transformation) in order to increase the accuracy when comparing the brain image to be examined with a standard brain image.
- linear transformation affine transformation
- a tissue separation process is performed (S13), and a white matter image and a gray matter image from which white matter and gray matter are extracted are created.
- the input T1-weighted MRI brain image includes three types of tissues: white matter that exhibits a high signal value corresponding to nerve fibers, gray matter that exhibits an intermediate signal value corresponding to nerve cells, and cerebrospinal fluid that exhibits a low signal value. Therefore, processing for extracting white matter and gray matter is performed by paying attention to the difference.
- This process is described in Patent Document 1.
- the integrated tissue separation process is performed with higher extraction accuracy than the method performed in Patent Document 1.
- the integrated tissue separation process is a tissue separation technique in which standardization, tissue separation, and signal non-uniformity correction are incorporated into one model. Details are described in Non-Patent Document 3.
- the integrated tissue separation process is characterized in that, in addition to the white matter image and the gray matter image, a conversion field indicating the correspondence between the coordinates of the MRI image and the coordinates of the standard brain is created. The conversion field is used for standardization described later.
- MRI brain images of many (multiple) healthy subjects are separated from each other, white matter images extracted from the white matter are created as samples, and white matter templates are created by spatial standardization among all the created samples.
- white matter images extracted from the white matter are created as samples
- white matter templates are created by spatial standardization among all the created samples.
- MRI brain images of a large number of healthy subjects are tissue-separated to create a gray matter image from which gray matter has been extracted as a sample, and a gray matter template is created by spatial standardization among all the created samples. .
- the DARTEL algorithm is applied to the spatial standardization performed here.
- DARTEL is superior in spatial standardization accuracy compared with the conventional VBM method, and is expected as a technique for improving diagnostic ability by image statistical analysis of Alzheimer's disease. Further, since DARTEL spatial standardization is performed more precisely than conventional methods, not only gray matter that has been evaluated until now but also white matter can be evaluated.
- a stratified template corresponding to the subject's attributes such as age and sex is created, and the white matter brain image template 32, gray matter brain image are stored in the database unit 30. Save as template 34.
- the white matter template and gray matter template are prepared according to age as shown in FIG.
- Gray matter (A) and white matter (C) were prepared based on images of healthy individuals aged 54 to 69 years, gray matter (B) and white matter (D) were 70 to 84 years old.
- the templates differ depending on the age. Particularly in the case of white matter, the size of the ventricle indicated by the arrow in the sixth template from the left is greatly different between (C) and (D). I understand that.
- the white matter template and the gray matter template are prepared for each gender as shown in FIG.
- the shape of the ventricles shows differences depending on gender.
- the diagnostic support information creation processing according to S1 to S7 is performed.
- the white and gray matter templates will be referred to as Darter templates.
- a T1-weighted MRI image captured in a slice shape having a predetermined thickness is input as a subject image, and the slice image is resampled so that the lengths of the sides of the voxel in each slice image are equal in advance. .
- the tissue separation process of S3 is performed.
- This tissue separation is the same as in S13, and white matter and gray matter are extracted to create a white matter image and a gray matter image of the subject.
- the spatial standardization process of S4 is performed on the white matter image and gray matter brain image of the subject created as described above.
- the Dartel algorithm is applied as in the case of S14.
- This spatial standardization process is a global correction for the entire brain size and a local correction for the partial size to absorb anatomical differences in brain images that exist between individuals. Is to do.
- the explanation will focus on gray matter, but substantially the same processing is also performed for white matter.
- the spatial standardization process at S4 Darter consists of the following three steps. (S4-1) Initial position determination process (S4-2) Conversion process to Darter template (S4-3) Conversion process to standard brain template
- the initial position is determined for the gray matter image and the white matter image using the conversion field to the standard brain obtained by the integrated tissue separation process described above.
- rigid body rigid ⁇ body
- the image subjected to the process in S4-1 is matched with the Darter template using the Darter algorithm.
- a process of matching the image combined with the Darter template obtained in S4-2 with the standard brain template is performed.
- a conversion field from the Dartel template to the standard brain template is obtained in advance, and conversion to the standard brain coordinate system is performed using the conversion field.
- the volume information is retained by performing the standardization while retaining the sum of the signal values of each voxel, the volume can be measured after the standardization.
- Step 3-2 will be described as an example.
- the average gray matter prepared in S14 read from the database unit 30 using linear transformation and nonlinear transformation as conceptually shown in FIG.
- Image processing is performed so that the sum of squares of errors with the brain image template 34 is minimized.
- a global correction of the position, size, and angle by linear transformation is performed, and then a shape such as local unevenness is corrected by nonlinear transformation.
- the linear transformation performed here is the same affine transformation as the alignment in S2.
- the non-linear transformation estimates a deformation field representing a local displacement in each of the x direction and the y direction, and converts the original image using this deformation field.
- the process of S4-2 is a process of matching the processing target image using the template created in S14 as a model, and the template to be used is created with high accuracy by applying the Dartel algorithm. Its shape is sharp.
- spatial standardization allows individual objects to be matched to a close shape without individual differences, so that the shape between individuals is almost the same, but atrophy is reflected in local density. As a result, the accuracy of spatial standardization can be improved.
- the image smoothing process of S5 is performed on the white matter image and the gray matter brain image (hereinafter also referred to as the standardized brain image) subjected to spatial standardization as described above.
- the FWHM (half width) of the filter used for smoothing is about 8 mm.
- Patent Document 1 a three-dimensional brain image and a three-dimensional convolution of a three-dimensional Gaussian function are performed. This is possible by sequentially performing one-dimensional convolution in the x, y, and z directions. By performing smoothing in this way, individual differences that do not completely match in the spatial standardization process can be reduced.
- FIG. 13 shows an image obtained as a result of the spatial standardization process in S4 and the smoothing process in S5 for the white matter image and the gray matter image separated in S3.
- the statistical comparison of S6 is performed.
- the MRI brain image of the gray matter (white matter) of the subject that has been standardized through each of the processes of S1 to S5 described above, and the healthy subject that has been collected and stored in the database unit 30 as the healthy subject image database 36
- a comparison test with the same MRI brain image group is performed. It is desirable that the healthy person image group to be used is composed of a subject close to the age of the subject.
- N is the total number of healthy subject images
- the Z score is a value obtained by scaling the difference between the voxel value of the subject image and the average voxel value of the corresponding voxel of the healthy subject image group by the standard deviation, and this is the gray matter (white matter) volume. It indicates the degree of relative decline.
- an appropriate critical value Z ′ is determined, and the Z score is Z ′ ⁇ Z (2)
- the voxels that satisfy the above are obtained, and the voxels exhibiting a statistically significant difference are obtained.
- Z ′ 2 that can be estimated to be abnormal with a probability of about 95% or more is used.
- the following formula is also used as a method for designating a critical value including all sites whose volume is lower than that of a healthy person. 0 ⁇ Z '(3)
- the healthy person image database 36 used in S6 has the spatial alignment of S2 to S5 for each of the healthy person image groups separately collected in advance ⁇ gray matter (white matter) tissue separation process ⁇ spatial
- Each process such as standardization ⁇ smoothing is sequentially performed and similarly created and stored.
- these collected healthy person images are classified by age, for example, every 5 years or every 10 years, and the average value and standard deviation calculated for each group are stored in a storage device. By storing it, it is possible to perform a test based on the Z score.
- the age of the subject is 76 years old, 74 to 78 years old (with a width of 5 years old). )) May be collected and compared.
- the analysis by the ROI in S7 is performed.
- This is a method of setting a region of interest (ROI) of a predetermined size on an image when determining the presence or absence of an abnormality using a brain image (see, for example, Non-Patent Document 5)
- ROI region of interest
- a ROI having a predetermined size is set at a specific part that is attracting attention as related to a specific disease, and comparison is performed.
- an ROI corresponding to a disease is obtained for a voxel at a coordinate position where a significant difference is found from a healthy person by the statistical processing and its Z score (evaluation value).
- Z score evaluation value
- ROI 38 as standardized image data corresponding to each disease such as Alzheimer is prepared, and for each disease considered from the symptoms of the subject, each ROI is included in the subject's brain image data. Is applied (set), and the most significant one is used as the diagnosis result based on the Z score in the ROI.
- P 1 sum of Z scores of voxels satisfying equation (3) in the ROI portion / number of voxels satisfying equation (3) in the ROI portion
- P 2 number of voxels satisfying equation (2) in the entire brain / total number of brains
- P 3 number of voxels satisfying formula (2) in the ROI portion / number of voxels in the ROI portion
- P 4 P 3 / P 2
- P 5 maximum Z score among all voxels in the ROI part
- characteristics in the patient group having the disease A are obtained in advance, and when the parameter value of the subject matches it, the subject is determined to be the disease A.
- a threshold value pathological condition identification value
- the subject is disease A when the parameter value obtained from the subject image exceeds the threshold value. That is, if the thresholds for identifying the pathological conditions of P 1 to P 4 are thP 1 to thP 5, respectively, P 1> thP 1, P 2> thP 2, P 3> thP 3, P 4> thP 4, P When at least one of 5> thP 5 is satisfied, the subject is determined as disease A. Specifically, for example, a case where determination is made by paying attention to only one parameter, such as P1, or a case where determination is made with reference to a part or all of P 1 to P 5 as necessary. it can.
- values limited to the right hemisphere side and the left hemisphere side may be obtained and added as parameters.
- the right / left ratio obtained by the equation (4) or the right / left difference obtained by the equation (5) may be added to the parameters with respect to the values on the right hemisphere side and the left hemisphere side.
- Right / left ratio (R ⁇ L) / (R + L) * 200 (4)
- Left-right difference RL (5)
- the value on the right hemisphere side is R
- the value on the left hemisphere side is L.
- ROI is determined based on statistical processing as follows. For example, in order to determine the ROI of a specific disease A, as shown in FIG. 16, an MRI image group (disease image group) of a patient with disease A and an image group (non- It is obtained by performing a two-sample t-test for statistically testing the significant difference between the two groups in units of voxels. Voxels that are significantly different by this test are regarded as characteristic voxels in the disease, and the set of coordinates is set as the ROI corresponding to the disease.
- the determination of the disease state identification value is performed by a general ROC (Receiver-Operating Characteristic) analysis for the disease.
- the ROC analysis is a general technique for quantitatively analyzing the ability to detect a disease for a certain test method.
- a method for obtaining the threshold thP1 in the case where the presence or absence of a disease is identified by the parameter P ⁇ ⁇ ⁇ ⁇ ⁇ 1 and the threshold thP 1 will be described below.
- One set of (TPF, FPF) is obtained for a certain thP1, and a plot of (TPF, FPF) obtained by varying this threshold value is the ROC curve illustrated in FIG. is there.
- the TPF is high and the FPF is low, but in the ROC curve, the upper left point corresponds to it.
- the threshold corresponding to the point D should be adopted.
- ⁇ T1-weighted images of the brains of subjects and healthy subjects are taken with the MRI apparatus, and each image is held in the DICOM format.
- the DICOM format is an image format generally used for medical images including a header portion and an image data portion in one file, and can store parameters and diagnostic information at the time of image capturing.
- one DICOM image file has information of one slice image, and a three-dimensional brain image is expressed by a plurality of DICOM images. DICOM images are stored on the DICOM server and can be retrieved as needed.
- the DICOM image file expresses the three-dimensional information of the entire brain by a plurality of sheets, but converts it to the Analyze format, which is a format in which only the header part of the DICOM file and only the image data part are connected.
- the entire brain for one person can be composed of two files, a header part file and an image data part file.
- SPM Statistical Parametric Mapping
- each of the processes of S1 to S7 in FIG. 2 was performed on the MRI brain image input from the subject.
- the template used for extraction of white matter and gray matter was the one created by ICBM (International Consortium® for Brain Mapping). This template is obtained by calculating the prior occurrence (existence) probabilities of white matter, gray matter, and cerebrospinal fluid from the brain images of a large number of healthy subjects, and has a voxel size of 2 mm square.
- pre-processing S11 to S14 and diagnostic support information creation processing S1 to S5 were performed.
- spatial standardization which has not been realized in the past, can be realized with high accuracy for white matter images, and by evaluating both gray matter lesions and white matter lesions, for example, Alzheimer-type dementia and vascular cognition. This is thought to improve the ability to distinguish symptom.
- an MRI brain image of a subject is input, a white matter image in which the white matter is extracted by separating the input MRI brain image is created.
- a standardized white matter image is created by spatial standardization based on a white matter template stored in advance, and the white matter of the subject is statistically compared with the white matter of a healthy subject based on the created standardized white matter image. Since the template was created by applying the Dartel algorithm to spatial standardization between white matter images of many healthy subjects, it was possible to create a highly accurate template for white matter, which has not been realized in the past As for white matter, it has become possible to provide objective diagnosis support for specific diseases.
- the input MRI brain image is tissue-separated to create a gray matter image from which the gray matter has been extracted, and the created gray matter image is spatially standardized based on a pre-stored gray matter template.
- the standard gray matter image was created using the standard gray matter image, and the subject gray matter was compared with the gray matter of the healthy subject based on the created standard gray matter image.
- the template can be created in the same way, and it is possible to provide more accurate diagnosis support for gray matter.
- white and gray matter templates are created and stored for each age and sex, so that spatial standardization is performed using a more appropriate template according to the age and sex of the subject. This makes it possible to achieve more accurate diagnosis support.
- the Dartel algorithm by using the Dartel algorithm, it has become possible to improve the accuracy of spatial standardization, which is conventionally limited to gray matter only, for white matter.
- the database unit 30 by creating a template according to age and gender in the database unit 30 and holding it, and selecting and applying a template suitable for the input image, it is possible to consider the influence of the subject's aging and gender. became.
- test method using a Z score as an evaluation value has been shown, the present invention is not limited to this, and a t score or the like used in other general tests may be used.
- the preparation processing in the present invention is not limited to the above embodiment, and can be applied to all brain images to be subjected to tissue separation.
- it can also be used as a pretreatment for gray matter tissue extraction accompanying tissue separation as shown in Patent Document 1.
- the preparation process (S11, S1) is executed before the spatial alignment (S12, S2) in both the preliminary preparation process and the basic process.
- the preparation process (S11, S1) may be executed after (S12, S2).
- the complicated slice image selection as described above is performed. No processing is required, and the upper brain part that is considered not to include high signal values other than the region around the skull and the brain parenchyma is specified. Specifically, what number slice image from the top is to be specified as the target slice.
- the preparation process shown in S1 and the diagnosis support information creation process shown in S2 to S7 are continuously executed in one medical image processing apparatus, and the preparation process shown in S11 and S12 are executed.
- the pre-processing shown in S14 is continuously executed in one medical image processing apparatus, but only the preparatory processing shown in S1 and S11 is executed in the medical image processing apparatus, and the result is obtained.
- the pre-processing and the diagnostic support information creation processing may be executed on the image after the high signal value suppression processing by another device. In this case, when the spatial alignment (S12, S2) is processed first, only the preparatory processes shown in S2, S1, S12, and S11 are executed in the medical image processing apparatus, and the result is obtained. Preprocessing and diagnosis support information creation processing are executed by another device on the image after the high signal value suppression processing.
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Theoretical Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Computer Vision & Pattern Recognition (AREA)
- General Health & Medical Sciences (AREA)
- Medical Informatics (AREA)
- Radiology & Medical Imaging (AREA)
- Quality & Reliability (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Pathology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- High Energy & Nuclear Physics (AREA)
- Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Geometry (AREA)
- Magnetic Resonance Imaging Apparatus (AREA)
- Image Processing (AREA)
Abstract
Description
Computed Tomography)やPET(Positron Emission Tomography)等の核医学検査や、CT(Computerized Tomography)やMRIによって脳の状態に関する情報が取得可能になってきている。
th1×(脳実質有効最大値Bmax)<(ピーク平均値Pave)
th2×(脳実質有効最大値Bmax)<(画像全体の有効最大値Imax)
s’(x,y)=th3
ただし、s(x,y)≧th3の場合に限る
s’(x,y)=th3+a(s(x、y)-th3)
ただし、s(x,y)≧th3の場合に限る
(S4-1) 初期位置決定処理
(S4-2) ダーテルテンプレートへの変換処理
(S4-3) 標準脳テンプレートへの変換処理
Z’<Z …(2)
となるようなボクセルを求め、統計的に有意な差が見られるボクセルとする。臨界値には、約95%以上の確率で異常と推定できるZ’=2を用いる。また、健常者よりも容積が低下している部位全てを含む臨界値の指定方法として、下記の式も用いる。
0<Z’ …(3)
P 1=ROI部分において式(3)を満たすボクセルのZスコアの合計/ROI部分において式(3)を満たすボクセルの数
P 2=脳全体において式(2)を満たすボクセルの数/脳全体のボクセル数
P 3=ROI部分において式(2)を満たすボクセルの数/ROI部分のボクセル数
P 4=P 3/P 2
P 5=ROI部分における全てのボクセルの中で最大のZスコア
左右比=(R-L)/(R+L)*200 …(4)
左右差= R-L …(5)
ただし、右半球側の値をR、左半球側の値をLとする。
TPF=TP/(TP+FN)
FPF=FP/(FP+TN)
20・・・画像・統計処理部
30・・・データベース部
32・・・白質脳画像テンプレート
34・・・灰白質脳画像テンプレート
36・・・健常者画像データベース
38・・・疾患特異的ROI
Claims (10)
- 複数のスライス画像で構成される脳画像から、処理対象とするスライス画像を対象スライスとして選択する対象スライス選択手段と、
脳実質の画素の信号値の有効最大値である脳実質有効最大値の計測処理を行う脳実質計測手段と、
脳画像全体の画素の信号値の有効最大値の計測処理を行う脳画像計測手段と、
頭蓋周辺領域のピークとなる画素の信号値の平均を頭蓋周回のピーク平均値として計測処理する頭蓋計測手段と、
計測された脳実質の有効最大値、脳画像全体の有効最大値、頭蓋周回のピーク平均値に基づいて、高信号値抑制処理が必要か不要かを判定する抑制処理判定手段と、
前記抑制処理判定手段により必要と判定された場合に、前記脳画像に対して高信号値抑制処理を実行する高信号値抑制処理手段と、
を有することを特徴とする医用画像処理装置。 - 前記抑制処理判定手段は、
前記脳実質有効最大値より頭蓋周回のピーク平均値が一定割合高いかどうかの判定である頭蓋領域判定と、
前記脳実質有効最大値より画像全体の信号値が一定割合高いかどうかの判定である画像全体判定と、を実行し、
前記頭蓋領域判定、画像全体判定のいずれか一方が条件を満たす場合に、高信号値抑制処理が必要と判定するものであることを特徴とする請求項1に記載の医用画像処理装置。 - 前記対象スライス選択手段は、各スライス画像について、画像内に所定の線分を設定し、この線分上に位置し、信号値が所定値以上となる画素のうち、最も離れた画素間の長さを求め、当該画素間の長さが全スライス画像中最長のものと比較して所定の比率以上となるスライス画像を対象スライスとして選択するものであることを特徴とする請求項1または請求項2に記載の医用画像処理装置。
- 前記脳実質計測手段は、選択された前記各対象スライスについて、脳の中心部を通る線分を所定数設定し、各線分ごとに線分上の画素の信号値分布を所定数の領域に分割し、中央の所定数の領域を脳実質領域として、当該脳実質領域における信号値のヒストグラムを求め、上位の所定の画素を除去した信号の最大値を脳実質の有効最大値として求めるものであることを特徴とする請求項1から請求項3のいずれか一項に記載の医用画像処理装置。
- 前記脳画像計測手段は、対象スライス全体の画素の信号値のヒストグラムを求め、上位の所定の画素を除去した信号の最大値を画像全体の有効最大値として求めるものであることを特徴とする請求項1から請求項4のいずれか一項に記載の医用画像処理装置。
- 前記頭蓋計測手段は、選択された前記各対象スライスについて、脳の中心部を通る線分を所定数設定し、各線分ごとに線分上の画素の信号値分布を所定数の領域に分割し、両端の所定数の領域を頭蓋周辺領域として、当該頭蓋周辺領域における信号最大値の、全ての対象スライスの全ての線分における平均値を頭蓋周回のピーク平均値として求めるものであることを特徴とする請求項1から請求項5のいずれか一項に記載の医用画像処理装置。
- 前記高信号値抑制処理手段は、信号値が所定値未満の画素については、その信号値を変更せず、信号値が前記所定値以上の画素については、信号値を所定値にする処理を実行することにより、相対的に高信号値抑制処理を実現するものであることを特徴とする請求項1から請求項6のいずれか一項に記載の医用画像処理装置。
- 前記高信号値抑制処理手段は、信号値が所定値未満の画素については、その信号値を変更せず、信号値が前記所定値以上の画素については、信号値を元の値より小さくなるように変換する処理を実行することにより、相対的に高信号値抑制処理を実現するものであることを特徴とする請求項1から請求項6のいずれか一項に記載の医用画像処理装置。
- 前記高信号値抑制処理手段は、信号値が所定値未満の画素については、その信号値を変更せず、信号値が前記所定値以上の画素については、信号値を傾きが零以上で1より小さい1次関数によって変換する処理を実行することにより、相対的に高信号値抑制処理を実現するものであることを特徴とする請求項8に記載の医用画像処理装置。
- 請求項1から請求項9のいずれか一項に記載の医用画像処理装置として、コンピュータを機能させるためのプログラム。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/991,012 US9042616B2 (en) | 2010-12-02 | 2011-12-01 | Medical image processing device |
JP2012546926A JP5601378B2 (ja) | 2010-12-02 | 2011-12-01 | 医用画像処理装置 |
EP11844823.2A EP2647335B1 (en) | 2010-12-02 | 2011-12-01 | Medical image processing device |
CN201180058114.6A CN103249358B (zh) | 2010-12-02 | 2011-12-01 | 医用图像处理装置 |
HK13114416.2A HK1186947A1 (en) | 2010-12-02 | 2013-12-31 | Medical image processing device |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010269073 | 2010-12-02 | ||
JP2010-269073 | 2010-12-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012074039A1 true WO2012074039A1 (ja) | 2012-06-07 |
Family
ID=46171964
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2011/077761 WO2012074039A1 (ja) | 2010-12-02 | 2011-12-01 | 医用画像処理装置 |
Country Status (6)
Country | Link |
---|---|
US (1) | US9042616B2 (ja) |
EP (1) | EP2647335B1 (ja) |
JP (1) | JP5601378B2 (ja) |
CN (1) | CN103249358B (ja) |
HK (1) | HK1186947A1 (ja) |
WO (1) | WO2012074039A1 (ja) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013066632A (ja) * | 2011-09-26 | 2013-04-18 | Dainippon Printing Co Ltd | 医用画像処理装置、医用画像処理方法、プログラム |
JP2016540602A (ja) * | 2013-12-19 | 2016-12-28 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | Dixonタイプ水/脂肪分離する磁気共鳴イメージング |
JP2017527788A (ja) * | 2014-07-15 | 2017-09-21 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | 個別化テンプレート画像による定位正則化を含むイメージングデータ統計的検定 |
JP2019005553A (ja) * | 2017-06-23 | 2019-01-17 | パナソニックIpマネジメント株式会社 | 情報処理方法、情報処理装置、および情報処理システム |
JP2020527258A (ja) * | 2017-07-22 | 2020-09-03 | インテリジェント ヴァイルス イメージング インコーポレイテッド | 電子顕微鏡写真における構造的外観の自動非監視下存在論的調査方法 |
WO2022065062A1 (ja) * | 2020-09-28 | 2022-03-31 | 富士フイルム株式会社 | 診断支援装置、診断支援装置の作動方法、診断支援装置の作動プログラム |
JP2023002822A (ja) * | 2017-06-23 | 2023-01-10 | パナソニックIpマネジメント株式会社 | 情報処理方法、情報処理装置、および情報処理システム |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012157201A1 (ja) * | 2011-05-18 | 2012-11-22 | 日本電気株式会社 | 情報処理システム、情報処理方法、情報処理装置およびその制御方法と制御プログラム |
US9332954B2 (en) * | 2013-03-15 | 2016-05-10 | Jacqueline K. Vestevich | Systems and methods for evaluating a brain scan |
CN105074778B (zh) * | 2013-03-28 | 2018-10-12 | 皇家飞利浦有限公司 | 交互式随访可视化 |
CN104143079B (zh) * | 2013-05-10 | 2016-08-17 | 腾讯科技(深圳)有限公司 | 人脸属性识别的方法和系统 |
ES2518690B1 (es) * | 2013-12-23 | 2015-09-29 | Centro De Investigación Biomédica En Red De Salud Mental (Cibersam) | Método para la detección de áreas anómalas en el cerebro a partir de imágenes de resonancia magnética |
JP2016064004A (ja) * | 2014-09-25 | 2016-04-28 | 大日本印刷株式会社 | 医用画像表示処理方法、医用画像表示処理装置およびプログラム |
EP3677191B1 (en) * | 2017-08-29 | 2023-09-20 | FUJIFILM Corporation | Information outputting device, method, and program |
JP7113447B2 (ja) * | 2018-03-12 | 2022-08-05 | 東芝エネルギーシステムズ株式会社 | 医用画像処理装置、治療システム、および医用画像処理プログラム |
JP7325310B2 (ja) | 2019-11-28 | 2023-08-14 | 富士フイルムヘルスケア株式会社 | 医用画像処理装置、医用画像解析装置、及び、標準画像作成プログラム |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07320028A (ja) * | 1994-05-24 | 1995-12-08 | Ge Yokogawa Medical Syst Ltd | 投影画像処理方法及び投影画像処理装置 |
JPH11507565A (ja) * | 1995-06-13 | 1999-07-06 | ブリティッシュ・テクノロジー・グループ・リミテッド | 画像改善装置及び方法 |
WO2007023522A1 (ja) * | 2005-08-22 | 2007-03-01 | National Center Of Neurology And Psychiatry | 脳疾患の診断支援方法及び装置 |
JP2007068852A (ja) * | 2005-09-08 | 2007-03-22 | Hitachi Medical Corp | 医用画像表示方法及び医用画像診断装置 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5845639A (en) * | 1990-08-10 | 1998-12-08 | Board Of Regents Of The University Of Washington | Optical imaging methods |
JP4025823B2 (ja) | 2004-02-24 | 2007-12-26 | 国立精神・神経センター総長 | 脳疾患の診断支援方法及び装置 |
EP1773194A1 (en) * | 2004-06-01 | 2007-04-18 | VAN ZIJL, Peter C.M. | Quantifying blood volume using magnetization transfer magnetic resonance imaging |
US20060177115A1 (en) * | 2005-02-04 | 2006-08-10 | Gifu University | Medical image processing apparatus and program |
US8112144B2 (en) * | 2006-03-30 | 2012-02-07 | National University Corporation Shizuoka University | Apparatus for determining brain atrophy, method of determining brain atrophy and program for determining brain atrophy |
WO2008000973A2 (fr) * | 2006-06-29 | 2008-01-03 | Centre National De La Recherche Scientifique - Cnrs | Méthode d'estimation du potentiel de croissance des infarctus cérébraux |
US20080187194A1 (en) * | 2007-02-05 | 2008-08-07 | Zhang Daoxian H | Cad image normalization |
US8185186B2 (en) * | 2007-04-13 | 2012-05-22 | The Regents Of The University Of Michigan | Systems and methods for tissue imaging |
US9804245B2 (en) * | 2007-06-29 | 2017-10-31 | Toshiba Medical Systems Corporation | Magnetic resonance imaging apparatus and magnetic resonance imaging method |
JP5229175B2 (ja) * | 2009-09-25 | 2013-07-03 | 大日本印刷株式会社 | 医用画像表示処理方法、装置およびプログラム |
-
2011
- 2011-12-01 WO PCT/JP2011/077761 patent/WO2012074039A1/ja active Application Filing
- 2011-12-01 US US13/991,012 patent/US9042616B2/en active Active
- 2011-12-01 JP JP2012546926A patent/JP5601378B2/ja active Active
- 2011-12-01 CN CN201180058114.6A patent/CN103249358B/zh active Active
- 2011-12-01 EP EP11844823.2A patent/EP2647335B1/en active Active
-
2013
- 2013-12-31 HK HK13114416.2A patent/HK1186947A1/xx not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07320028A (ja) * | 1994-05-24 | 1995-12-08 | Ge Yokogawa Medical Syst Ltd | 投影画像処理方法及び投影画像処理装置 |
JPH11507565A (ja) * | 1995-06-13 | 1999-07-06 | ブリティッシュ・テクノロジー・グループ・リミテッド | 画像改善装置及び方法 |
WO2007023522A1 (ja) * | 2005-08-22 | 2007-03-01 | National Center Of Neurology And Psychiatry | 脳疾患の診断支援方法及び装置 |
JP2007068852A (ja) * | 2005-09-08 | 2007-03-22 | Hitachi Medical Corp | 医用画像表示方法及び医用画像診断装置 |
Non-Patent Citations (6)
Title |
---|
ASHBUMER J, A: "fast diffeomorphic image registration algorithm", NEUROIMAGE, vol. 38, no. 1, 15 October 2007 (2007-10-15), pages 95 - 113 |
BOOKSTEIN FL: "Voxel-based morphometry", NEUROIMAGE, vol. 14, no. 6, 2001, pages 1454 - 62 |
HIROSHI MATSUDA: "Image Diagnosis of Alzheimer's Dementia", 2001, MEDICAL VIEW CO., LTD., article "Statistical Analysis of SPECT", pages: 76 - 86 |
J.ASHBUMER; K.J.FRISTON: "Unified segmentation", NEUROIMAGE, vol. 26, 2005, pages 839 - 851 |
See also references of EP2647335A4 |
YOKO HIRATA; HIROSHI MATSUDA; KIYOTAKA NEMOTO; TAKASHI OHNISHI; KENTARO HIRAO; FUMIO YAMASHITA; TAKASHI ASADA; SATOSHI IWABUCHI; H: "Voxel-based morphometry to discriminate early Alzheimer's disease from controls", NEUROSCI LETT, vol. 382, 2005, pages 269 - 274 |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013066632A (ja) * | 2011-09-26 | 2013-04-18 | Dainippon Printing Co Ltd | 医用画像処理装置、医用画像処理方法、プログラム |
JP2016540602A (ja) * | 2013-12-19 | 2016-12-28 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | Dixonタイプ水/脂肪分離する磁気共鳴イメージング |
JP2017527788A (ja) * | 2014-07-15 | 2017-09-21 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | 個別化テンプレート画像による定位正則化を含むイメージングデータ統計的検定 |
JP2019005553A (ja) * | 2017-06-23 | 2019-01-17 | パナソニックIpマネジメント株式会社 | 情報処理方法、情報処理装置、および情報処理システム |
US11445920B2 (en) | 2017-06-23 | 2022-09-20 | Panasonic Intellectual Property Management Co., Ltd. | Information processing method, information processing device, and information processing system |
JP7178614B2 (ja) | 2017-06-23 | 2022-11-28 | パナソニックIpマネジメント株式会社 | 情報処理方法、情報処理装置、および情報処理システム |
JP2023002822A (ja) * | 2017-06-23 | 2023-01-10 | パナソニックIpマネジメント株式会社 | 情報処理方法、情報処理装置、および情報処理システム |
JP7312977B2 (ja) | 2017-06-23 | 2023-07-24 | パナソニックIpマネジメント株式会社 | 情報処理方法、情報処理装置、および情報処理システム |
US12029530B2 (en) | 2017-06-23 | 2024-07-09 | Panasonic Intellectual Property Management Co., Ltd. | Information processing method, information processing device, and information processing system |
JP2020527258A (ja) * | 2017-07-22 | 2020-09-03 | インテリジェント ヴァイルス イメージング インコーポレイテッド | 電子顕微鏡写真における構造的外観の自動非監視下存在論的調査方法 |
WO2022065062A1 (ja) * | 2020-09-28 | 2022-03-31 | 富士フイルム株式会社 | 診断支援装置、診断支援装置の作動方法、診断支援装置の作動プログラム |
Also Published As
Publication number | Publication date |
---|---|
EP2647335A1 (en) | 2013-10-09 |
JP5601378B2 (ja) | 2014-10-08 |
JPWO2012074039A1 (ja) | 2014-05-19 |
CN103249358A (zh) | 2013-08-14 |
US9042616B2 (en) | 2015-05-26 |
EP2647335B1 (en) | 2020-06-03 |
US20130251231A1 (en) | 2013-09-26 |
CN103249358B (zh) | 2015-09-09 |
EP2647335A4 (en) | 2017-11-08 |
HK1186947A1 (en) | 2014-03-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5601378B2 (ja) | 医用画像処理装置 | |
JP5699936B2 (ja) | 医用画像処理装置の作動方法、装置およびプログラム | |
JP4025823B2 (ja) | 脳疾患の診断支援方法及び装置 | |
JP6036009B2 (ja) | 医用画像処理装置、およびプログラム | |
JP5695648B2 (ja) | 医用画像処理方法および装置 | |
EP2790575B1 (en) | Method and apparatus for the assessment of medical images | |
JP5098393B2 (ja) | 関心領域決定装置 | |
WO2016047683A1 (ja) | 医用画像表示処理方法、医用画像表示処理装置およびプログラム | |
CN100561518C (zh) | 基于感兴趣区域的自适应医学序列图像插值方法 | |
WO2007023522A1 (ja) | 脳疾患の診断支援方法及び装置 | |
KR20130136519A (ko) | 파노라마 엑스선 사진을 이용한 진단 지원 시스템, 및 파노라마 엑스선 사진을 이용한 진단 지원 프로그램 | |
US20130303900A1 (en) | Method and apparatus for processing of stroke ct scans | |
JP4022587B2 (ja) | 脳疾患の診断支援方法及び装置 | |
JP6705528B2 (ja) | 医用画像表示処理方法、医用画像表示処理装置およびプログラム | |
CN114847922A (zh) | 一种基于纤维束自动识别的脑年龄预测方法 | |
Somasundaram et al. | Brain extraction method for T1-weighted magnetic resonance scans | |
JP4721693B2 (ja) | 頭蓋内容積および局所脳構造物解析プログラム、記録媒体および頭蓋内容積および局所脳構造物解析方法 | |
Paniagua et al. | 3D of brain shape and volume after cranial vault remodeling surgery for craniosynostosis correction in infants | |
US11324413B1 (en) | Traumatic brain injury diffusion tensor and susceptibility weighted imaging | |
CN114862799B (zh) | 一种用于flair-mri序列的全自动脑体积分割方法 | |
EP3624058A1 (en) | Method and system of analyzing symmetry from image data | |
KR102349360B1 (ko) | 영상 진단기기를 이용한 특발성 정상압 수두증의 진단 방법 및 시스템 | |
KR101455198B1 (ko) | Ct 영상 분석을 이용한 흉곽 변형성 정량적 평가 지표값 계산 방법, 시스템 및 기록 매체 | |
JP2023552547A (ja) | 拡散強調磁気共鳴画像から胎児の脳室容積を判定するためのコンピュータ実装方法及びシステム、並びに関連するnmr脳室容積評価方法 | |
CN117838089A (zh) | 基于磁共振成像的大脑海马体分析方法、系统及电子设备 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11844823 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2012546926 Country of ref document: JP Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13991012 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011844823 Country of ref document: EP |