[反映临床表型的综合凝血检测方法的发展]。

Tomoko Matsumoto, Keiji Nogami
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引用次数: 0

摘要

PT、APTT、凝血因子活性用基于凝血时间的方法测定。当凝血和纤溶增强时,可以检测到TAT和PIC,但很难评估它们的功能低下状态。设计了一种实时、全面、连续地评价凝血和纤溶的新方法。我们通过以下方法阐明了先天性和获得性凝血障碍的临床表型;(1)血块波形分析(CWA)评价纤维蛋白形成;(2)凝血酶生成试验(TGT),监测纤维蛋白形成前的一步。(3)凝血酶/纤溶酶生成测定(T/P-G)与TGT同时评估纤溶。结果表明:(1)CWA能够检测到非常低的FVIII活性水平(FVIII:C 0.2 ~ 1.0 IU/dL),并检测到明显严重的FVIII:C型
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[Development of Comprehensive Coagulation Assays Reflecting the Clinical Phenotype].

PT, APTT, and coagulation factor activity are measured with clotting time-based methods. When coagula- tion and fibrinolysis are enhanced, TAT and PIC are detected, but evaluations of their hypofunctional state are difficult. We devised a new method that can be used to comprehensively and continuously evaluate coagula- tion and fibrinolysis in real time. We elucidated the clinical phenotype of congenital and acquired coagulation disorders using the following methods; (1) Clot waveform analysis (CWA) to evaluate fibrin formation; (2) Thrombin generation test (TGT) to monitor one-step before fibrin formation. (3) Thrombin/Plasmin generation assay (T/P-G) to evaluate fibrinolysis simultaneously with TGT. The results revealed that (1) CWA enabled the measurement of a very low FVIII activity level (FVIII:C 0.2-1.0 IU/dL) and detected a markedly severe type with FVIII:C <0.2 IU/dL. (2) For TGT, acquired hemophilia A showed a much lower value than that of congenital severe hemophilia A, being consistent with its severe bleeding. (3) CWA parameters for acquired factor V inhibitors in patients with bleeding symptoms were more impaired than with non-bleeding. Taken together these comprehensive assays can reflect the clinical phenotype and make it possible to analyze unidentified coagulation/fibrinolysis abnormality.

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[Candida]. [Bleeding time]. [Microparticle]. [Aldolase]. [Telomerase].
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