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凝血酶生成试验的标准化及临床应用

Standardization and clinical utility of thrombin-generation assays.

作者信息

Berntorp Erik, Salvagno Gian Luca

机构信息

Malmö Centre for Thrombosis and Haemostasis, Malmö University Hospital, Malmö, Sweden.

出版信息

Semin Thromb Hemost. 2008 Oct;34(7):670-82. doi: 10.1055/s-0028-1104546. Epub 2008 Dec 15.

Abstract

Thrombin generation is a key process that determines the extent of a hemostatic plug or a thrombotic process. The ensuing thrombin burst is crucial for the formation of a stable fibrin clot. During its active life, thrombin exerts a multitude of highly regulated actions on the blood and the vessel wall, including the clotting of fibrinogen. The inappropriate generation of thrombin may lead to pathologic processes, foremost of which are hemorrhagic or thrombotic diseases. The coagulation system is usually investigated by means of two in vitro classic clotting tests, the activated partial thromboplastin time (APTT) and prothrombin time (PT), which assess only time to initiation of clot formation and do not entirely reflect global hemostatic balance. The APTT and PT permit identification of connectivity between the component activities identified as required for plasma coagulation and define the concept of intrinsic and extrinsic coagulation pathways, which converge at the point of formation of the prothrombinase complex. However, the mechanisms established by in vitro tests are not always mirrored in the human pathologies associated with bleeding or thrombosis. The recent development of newer tests based on the continuous registration of thrombin generation under in vitro conditions that mimic more closely what occurs in vivo prompt a reinvestigation of the balance between procoagulants and anticoagulants in patients with various hemostatic disorders. Thrombin-generation assays not only provide an overall assessment of hemostasis but also target potential extrahemostatic effects of the generated thrombin, a potent agonist of a multitude of cellular activation pathways. Moreover, estimation of an individual's thrombin-generation potential may correlate more closely with a hypercoagulable or hypocoagulable phenotype when compared with traditional coagulation tests. In this review, we discuss to what extent thrombin generation can be expected to reflect the clotting function of blood, the development and use of different thrombin-generation assay systems suitable for detecting changes in the kinetics of thrombin generation, and the clinical utility of thrombin generation.

摘要

凝血酶生成是决定止血栓形成程度或血栓形成过程的关键过程。随之而来的凝血酶爆发对于稳定纤维蛋白凝块的形成至关重要。在其活跃期,凝血酶对血液和血管壁发挥多种高度调节的作用,包括纤维蛋白原的凝血作用。凝血酶的不适当生成可能导致病理过程,其中最主要的是出血性或血栓性疾病。凝血系统通常通过两种体外经典凝血试验进行研究,即活化部分凝血活酶时间(APTT)和凝血酶原时间(PT),这两种试验仅评估凝血形成开始的时间,并不完全反映整体止血平衡。APTT和PT能够确定血浆凝血所需的各组分活性之间的关联性,并定义内源性和外源性凝血途径的概念,这两条途径在凝血酶原酶复合物形成点汇合。然而,体外试验所确立的机制并不总是反映在与出血或血栓形成相关的人类病理情况中。基于在更接近体内发生情况的体外条件下连续记录凝血酶生成的新型试验的最新进展,促使人们重新研究各种止血障碍患者体内促凝血剂和抗凝剂之间的平衡。凝血酶生成测定不仅能全面评估止血情况,还能针对所生成凝血酶的潜在非止血作用,凝血酶是多种细胞激活途径的强效激动剂。此外,与传统凝血试验相比,估计个体的凝血酶生成潜力可能与高凝或低凝表型更密切相关。在本综述中,我们讨论了凝血酶生成在多大程度上有望反映血液的凝血功能、适用于检测凝血酶生成动力学变化的不同凝血酶生成测定系统的开发和应用,以及凝血酶生成的临床实用性。

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