Division of Angiology and Haemostasis, University Hospital, Geneva, Switzerland.
Semin Thromb Hemost. 2010 Feb;36(1):7-17. doi: 10.1055/s-0030-1248720. Epub 2010 Apr 13.
Fibrinogen contributes to thrombosis risk in different ways. Indeed, various mutations in the fibrinogen genes predispose to thrombosis. At the same time, high levels of fibrinogen are also associated with thrombotic complications. Although the underlying causative mechanisms are not clear, this most likely involves the associated inflammatory and hypercoagulable states. In the last few years, particular attention has focused on the polymorphisms of fibrinogen genes involved in increased fibrinogen levels or fibrinogen qualitative changes. The association between dysfibrinogenemia and risk of thrombosis is well known, and some mechanisms have been clearly identified. Paradoxically, some patients with either hypofibrinogenemia or afibrinogenemia may also suffer from severe thromboembolic complications. The management of these patients is particularly challenging because they are not only at risk of thrombosis but also of bleeding. This review discusses the various quantitative and qualitative defects of fibrinogen associated with thrombosis, the tests that may predict the thrombotic risk, as well as some preventive or therapeutic approaches.
纤维蛋白原通过不同方式导致血栓形成风险。事实上,纤维蛋白原基因的各种突变可导致血栓形成。同时,纤维蛋白原水平升高也与血栓形成并发症相关。尽管潜在的致病机制尚不清楚,但这很可能涉及相关的炎症和高凝状态。在过去几年中,人们特别关注与纤维蛋白原水平升高或纤维蛋白原性质改变相关的纤维蛋白原基因多态性。纤维蛋白原血症与血栓形成风险之间的关联是众所周知的,一些机制已被明确识别。矛盾的是,一些低纤维蛋白原血症或无纤维蛋白原血症患者也可能患有严重的血栓栓塞并发症。这些患者的管理极具挑战性,因为他们不仅有血栓形成的风险,而且有出血的风险。这篇综述讨论了与血栓形成相关的纤维蛋白原的各种定量和定性缺陷、可能预测血栓形成风险的检测方法,以及一些预防或治疗方法。