Rao A K, Kaplan R, Sheth S
Division of Hematology and Thromboembolic Diseases and the Sol Sherry Thrombosis Research Center, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Semin Thromb Hemost. 1998;24 Suppl 1:3-12.
Thrombophilic states are a group of conditions associated with increased predisposition to thromboembolic events. The well-recognized inherited thrombophilic states include resistance to activated protein C (APC) (Factor V Leiden) and deficiencies of plasma antithrombin, protein C, and protein S. These entities are aberrations in the natural anticoagulant systems that exist in plasma and at the endothelial cell level. Other causes of inherited thrombophilia include hyperhomocysteinemia, abnormalities in the proteins of the fibrinolytic system, dysfibrinogenemias, deficiency of heparin cofactor II, abnormal thrombomodulin, and the recently described variation in the prothrombin gene. Most of the inherited abnormalities recognized to date are associated with venous thromboembolism (VTE) rather than arterial thrombosis. Approximately half of VTE episodes in patients with inherited thrombophilias occur in relation to events that are generally recognized as predisposing states, such as surgery, pregnancy, and immobilization. In this review, the risks of VTE associated with inherited risk factors are discussed, and guidelines for the diagnosis and management are presented.
易栓症是一组与血栓栓塞事件易感性增加相关的病症。公认的遗传性易栓症包括对活化蛋白C(APC)的抵抗(因子V莱顿突变)以及血浆抗凝血酶、蛋白C和蛋白S的缺乏。这些实体是血浆和内皮细胞水平存在的天然抗凝系统的异常。遗传性血栓形成倾向的其他原因包括高同型半胱氨酸血症、纤维蛋白溶解系统蛋白异常、异常纤维蛋白原血症、肝素辅因子II缺乏、血栓调节蛋白异常以及最近描述的凝血酶原基因变异。迄今为止认识到的大多数遗传性异常与静脉血栓栓塞(VTE)而非动脉血栓形成有关。遗传性易栓症患者中约一半的VTE发作与通常被认为是诱发状态的事件有关,如手术、妊娠和制动。在本综述中,讨论了与遗传风险因素相关的VTE风险,并提出了诊断和管理指南。