ES2652495T3 - Método para detectar anticoagulantes lúpicos - Google Patents

Método para detectar anticoagulantes lúpicos Download PDF

Info

Publication number
ES2652495T3
ES2652495T3 ES12800902.4T ES12800902T ES2652495T3 ES 2652495 T3 ES2652495 T3 ES 2652495T3 ES 12800902 T ES12800902 T ES 12800902T ES 2652495 T3 ES2652495 T3 ES 2652495T3
Authority
ES
Spain
Prior art keywords
blood
sample
time
coagulation
blood sample
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
ES12800902.4T
Other languages
English (en)
Inventor
Masahiro IEKO
Chizuru Morikawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SCHOOL JURIDICAL PERSON HIGASHI-NIPPON-GAKUEN
Sekisui Medical Co Ltd
Original Assignee
SCHOOL JURIDICAL PERSON HIGASHI-NIPPON-GAKUEN
Sekisui Medical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SCHOOL JURIDICAL PERSON HIGASHI-NIPPON-GAKUEN, Sekisui Medical Co Ltd filed Critical SCHOOL JURIDICAL PERSON HIGASHI-NIPPON-GAKUEN
Application granted granted Critical
Publication of ES2652495T3 publication Critical patent/ES2652495T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/86Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood coagulating time or factors, or their receptors
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/56Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving blood clotting factors, e.g. involving thrombin, thromboplastin, fibrinogen
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/564Immunoassay; Biospecific binding assay; Materials therefor for pre-existing immune complex or autoimmune disease, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00Detection or diagnosis of diseases
    • G01N2800/10Musculoskeletal or connective tissue disorders
    • G01N2800/101Diffuse connective tissue disease, e.g. Sjögren, Wegener's granulomatosis
    • G01N2800/104Lupus erythematosus [SLE]
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00Detection or diagnosis of diseases
    • G01N2800/24Immunology or allergic disorders

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Urology & Nephrology (AREA)
  • Biochemistry (AREA)
  • Analytical Chemistry (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biotechnology (AREA)
  • Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Food Science & Technology (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Medicinal Chemistry (AREA)
  • Cell Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Rehabilitation Therapy (AREA)
  • Biophysics (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

Un método para detectar anticoagulantes lúpicos, comprendiendo el método las siguientes etapas (A), (B) y (C): (A) añadir una composición solución tampón que contiene factores de coagulación sanguínea a cada una de una muestra de sangre y una muestra diluida de la muestra de sangre antes de la medición o en el momento de la medición del tiempo de coagulación sanguínea; (B) medir los tiempos de coagulación sanguínea para las diversas muestras de la etapa (A); y (C) comparar los tiempos de coagulación sanguínea para las diversas muestras obtenidas en la etapa (B), donde cuando la relación (tiempo de coagulación de la muestra diluida) / (tiempo de coagulación de la muestra de sangre) es menor de un valor de corte calculado a partir de valores medidos de plasmas de personas sanas sin anormalidad de coagulación, la muestra de sangre se considera que es positiva para anticoagulante lúpico.

Description

imagen1
imagen2
imagen3
imagen4
imagen5
imagen6
imagen7
Como se enumera en la Tabla 4, en los plasmas de pacientes deficientes en factor de coagulación (FVIII y FIX) en los que se niega la presencia de AL, los valores resultado fueron mayores de o iguales al valor de corte en el ensayo de cribado de TTPA, de manera que es difícil la discriminación de la positividad de AL. Por otro lado, en el ensayo de TVVRd, el ensayo de mezcla, y los Inventos 1 y 2, los valores resultado eran todos negativos. El método de la presente invención implica un sistema en el que los factores de coagulación se complementan a un plasma de ensayo; sin embargo, puesto que el método incluye un proceso de comparación de los valores obtenidos antes y después de la dilución, los resultados obtenidos en un estado en el que simplemente los factores de coagulación son deficientes, y los resultados en el caso que es positivo a inhibidor no son ambiguos. La discriminación se puede hacer claramente como en el caso del ensayo de TVVRd o el ensayo de mezcla.
imagen8
Como se enumera en la Tabla 5, en el grupo de administrado con heparina/no AL, los valores resultado en siete ejemplos de ocho ejemplos son todos mayores de o iguales al valor de corte en el ensayo de cribado de TTPA, de manera que es difícil la discriminación a partir de la positividad de AL. Además, en el ensayo de TVVRd, dos ejemplos de ocho ejemplos mostraron falsa positividad (en la tabla, indicado como “positivo*”). Por otro lado, los resultados eran todos negativos en las Invenciones 1 y 2.
imagen9
imagen10
imagen11
imagen12
imagen13
imagen14
imagen15

Claims (1)

  1. imagen1
ES12800902.4T 2011-06-17 2012-06-15 Método para detectar anticoagulantes lúpicos Active ES2652495T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2011135173 2011-06-17
JP2011135173 2011-06-17
PCT/JP2012/065433 WO2012173259A1 (ja) 2011-06-17 2012-06-15 ループスアンチコアグラントの検出方法

Publications (1)

Publication Number Publication Date
ES2652495T3 true ES2652495T3 (es) 2018-02-02

Family

ID=47357237

Family Applications (1)

Application Number Title Priority Date Filing Date
ES12800902.4T Active ES2652495T3 (es) 2011-06-17 2012-06-15 Método para detectar anticoagulantes lúpicos

Country Status (7)

Country Link
US (1) US9977038B2 (es)
EP (1) EP2722674B1 (es)
JP (1) JP6028314B2 (es)
KR (1) KR101979865B1 (es)
CA (1) CA2839117C (es)
ES (1) ES2652495T3 (es)
WO (1) WO2012173259A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE540132C2 (sv) 2014-05-22 2018-04-10 Zafena Ab Analysmetod för bestämning av antikoagulanter i blod eller blodplasma
JP6499488B2 (ja) * 2015-03-31 2019-04-10 学校法人東日本学園 凝固時間の測定方法、ループスアンチコアグラントの存否の判定方法及びループスアンチコアグラント検出用試薬キット
JP6837851B2 (ja) * 2017-01-31 2021-03-03 シスメックス株式会社 血液検体の判定方法、並びに血液検体の分析のための装置及びコンピュータプログラム
JP6873833B2 (ja) * 2017-06-09 2021-05-19 シスメックス株式会社 血液検体の判定方法、血液検体分析装置及びコンピュータプログラム

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5543145A (en) * 1984-09-17 1996-08-06 Baxter International, Inc. Pharmaceutical composition and method for the suppression of factor VIII inhibitor production
JPH0650999B2 (ja) 1988-09-12 1994-07-06 日本商事株式会社 血液凝固因子安定化法
US4877741A (en) 1988-10-24 1989-10-31 The United States Of America As Represented By The Secretary Of The Air Force Treatment of human plasma with brown recluse spider toxin to emulate a lupus anticoagulant
EP1562047B1 (en) * 2004-02-06 2008-05-14 Sysmex Corporation Reagent kit for detecting lupus anticoagulant
US7932021B2 (en) * 2005-07-28 2011-04-26 American Diagnostica, Inc. Lupus anticoagulant testing
CN101221189B (zh) 2007-01-12 2012-08-15 上海太阳生物技术有限公司 一种用于测定活化部分凝血活酶时间aptt的体外诊断试剂盒
CN102066947B (zh) 2008-06-18 2015-10-14 积水医疗株式会社 凝血时间延长原因的判定方法

Also Published As

Publication number Publication date
EP2722674A1 (en) 2014-04-23
JPWO2012173259A1 (ja) 2015-02-23
CA2839117A1 (en) 2012-12-20
US20140127725A1 (en) 2014-05-08
JP6028314B2 (ja) 2016-11-16
KR20140034230A (ko) 2014-03-19
EP2722674A4 (en) 2015-02-25
WO2012173259A1 (ja) 2012-12-20
EP2722674B1 (en) 2017-11-29
US9977038B2 (en) 2018-05-22
CN103649758A (zh) 2014-03-19
CA2839117C (en) 2019-09-17
KR101979865B1 (ko) 2019-05-17

Similar Documents

Publication Publication Date Title
Martinuzzo et al. Frequent false‐positive results of lupus anticoagulant tests in plasmas of patients receiving the new oral anticoagulants and enoxaparin
ES2652495T3 (es) Método para detectar anticoagulantes lúpicos
Merriman et al. Rivaroxaban and false positive lupus anticoagulant testing
Mani et al. Ex vivo effects of low-dose rivaroxaban on specific coagulation assays and coagulation factor activities in patients under real life conditions
Antovic et al. Effects of direct oral anticoagulants on lupus anticoagulant assays in a real-life setting
JP4505045B2 (ja) 血液凝固時間の延長原因の判定法
BR112015004878A2 (pt) dispositivo e método para determinar se as condições predeterminadas para medir um primeiro parâmetro fisiológico de um indivíduo são atendidas, e, vestimenta para ser vestida pelo indivíduo
JP2014209134A5 (es)
Chojnowski et al. Effects of rivaroxaban therapy on ROTEM coagulation parameters in patients with venous thromboembolism
Pouplard et al. The Taipan snake venom time can be used to detect lupus anticoagulant in patients treated by rivaroxaban.
Blaine et al. Viscoelastic monitoring to guide the correction of perioperative coagulopathy and massive transfusion in patients with life-threatening hemorrhage
Zalewski et al. Rivaroxaban concentration in patients with deep vein thrombosis who reported thrombus progression or minor hemorrhagic complications: first Polish experience
CA2883260C (en) Composition for use as an abnormal coagulation control plasma in in vitro assays
BR112015032574A2 (pt) captura de erro de sinal transiente para uma medição de analito determinada a partir de um tempo de amostragem especificado derivado de uma característica física detectada da amostra contendo o analito
ES2530357T3 (es) Método para detectar una infección con plasmodio
BR112015032567A2 (pt) supressor de erro de preenchimento para uma medição de analito determinada a partir de um tempo de amostragem especificado derivado de uma característica física detectada da amostra contendo o analito
BR112014027411A2 (pt) detecção de ativação do complemento
Geddings et al. Comment on “Tissue factor expressed by microparticles is associated with mortality but not with thrombosis in cancer patients”
EA201690995A1 (ru) Способы обнаружения и количественного анализа циркулирующих эндотелиальных клеток
Yokuş et al. Evaluation of risk factors for thrombophilia in patients with cerebral venous thrombosis.
Cappellano et al. Circulating Platelet-Derived Extracellular Vesicles Are a Hallmark of Sars-Cov-2 Infection. Cells. 2021; 10: 85
Al-Maktari et al. Thrombotic events in patients with sickle cell anemia: relationship to Protein C, S and total homocysteine levels
Atalay et al. sEPCR Levels in Chronic Myeloproliferative Diseases and Their Association with Thromboembolic Events: A Case-Control Study
Góralczyk et al. False-positive lupus anticoagulant in patients receiving rivaroxaban: 24▊h since the last dose are needed to exclude antiphospholipid syndrome
TH140064A (th) วิธีการสำหรับการตรวจวัดสารต้านการจับก้อนของรอยแผล