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2014 Fiscal Year Final Research Report

Analysis of the pathology and regulation system in pregnancy-associated thrombotic microangiopathy (TMA)

Research Project

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Project/Area Number 23591425
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Hematology
Research InstitutionNara Medical University

Principal Investigator

FUJIMURA Yoshihiro  奈良県立医科大学, 医学部, 名誉教授 (80118033)

Co-Investigator(Kenkyū-buntansha) MATSUMOTO Masanori  奈良県立医科大学, 輸血部, 教授 (60316081)
SADO Toshiyuki  奈良県立科大学, 産婦人科, 講師 (50275335)
HAYAKAWA Masaki  奈良県立医科大学, 輸血部, 医員 (30516729)
Project Period (FY) 2011-04-28 – 2015-03-31
Keywords妊娠関連TMA / HELLP症候群 / ADAMTS13 / VEF / 胎盤由来E-NTPDase
Outline of Final Research Achievements

In this study, we aimed to reveal the pathology of pregnancy-associated thrombotic microangiopathy (TMA). We analyzed von Willebrand factor (VWF), VWF-cleaving specific cleavage protease ADAMTS13 and placenta-derived E-NTPDase by using the plasma samples of normal pregnant women and the patients with pregnancy-induced hypertension (PIH) or HELLP syndrome.
We identified that the patients with HELLP syndrome had the severe deletion of "VWF unbound forms of ADAMTS13 (free ADAMTS13)" in isoelectric focusing. We previously showed that cryosupernatant, which abundantly contains “free ADAMTS13”, inhibited initial phase of platelet aggregation. Thus, we suggested that the development of HELLP syndrome might be associated with the decreased function of inhibiting initial phase of platelet aggregation by “free ADAMTS13”.

Free Research Field

血栓止血学

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Published: 2016-06-03  

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