Department of Pathology and Molecular Medicine, 201 Richardson Laboratory, Queen's University, Kingston, Ontario, K7L 3N6 Canada.
Thromb Haemost. 2013 Jan;109(1):53-60. doi: 10.1160/TH12-05-0316. Epub 2012 Nov 22.
Factor VIII (FVIII), a procoagulant cofactor, plays a crucial role in the intrinsic coagulation cascade. A causal association between elevated FVIII levels and venous thrombosis incidence has been established; no such association has been confirmed with arterial thrombosis. The independent role of elevated FVIII levels in arteriolar thrombosis was evaluated in a mouse model to determine the thrombogenic potential of elevated levels of FVIII. The in vitro thrombogenic effect of elevated FVIII levels was examined using thrombin-antithrombin (TAT) complex generation and thromboelastography (TEG) assays. The thrombogenic potential of acute and extended elevation of circulating FVIII levels was assessed using ferric chloride induced injury of the cremaster arterioles. The rate of TAT complex formation, and the final concentration of TAT complexes, significantly increased as FVIII levels were elevated from 100% to 400% FVIII activity. TEG analysis of fibrin and clot formation showed that as FVIII levels were elevated, the time to initial fibrin formation decreased and the rate of fibrin formation increased. The acute elevation of circulating FVIII to 400% FVIII activity resulted in significantly decreased times to vessel occlusion. Prolonged elevation of FVIII activity did not significantly affect time to vessel occlusion. In conclusion, acute elevations in FVIII levels result in a non-linear thrombogenic effect, with non-significant increases in thrombogenic risk within the physiological range (FVIII levels up to 200%). Prolonged elevation of plasma FVIII did not further increase the thrombogenic potential of elevated FVIII levels.
VIII 因子(FVIII)是一种促凝辅助因子,在内在凝血级联反应中起着至关重要的作用。已经证实升高的 FVIII 水平与静脉血栓形成的发生率之间存在因果关系;而与动脉血栓形成则没有得到证实。在小鼠模型中评估了升高的 FVIII 水平在小动脉血栓形成中的独立作用,以确定升高的 FVIII 水平的血栓形成潜力。使用凝血酶-抗凝血酶(TAT)复合物生成和血栓弹性描记图(TEG)测定来检查升高的 FVIII 水平的体外血栓形成作用。使用氯化铁诱导的提睾肌小动脉损伤来评估循环 FVIII 水平的急性和延长升高的血栓形成潜力。TAT 复合物形成的速率以及 TAT 复合物的最终浓度随着 FVIII 水平从 100%升高到 400%的 FVIII 活性而显著增加。TEG 分析纤维蛋白和血凝块形成表明,随着 FVIII 水平的升高,初始纤维蛋白形成的时间减少,纤维蛋白形成的速度增加。循环 FVIII 急性升高至 400%FVIII 活性导致血管闭塞时间显著缩短。FVIII 活性的延长升高并未显著影响血管闭塞时间。总之,急性升高的 FVIII 水平导致非线性血栓形成作用,在生理范围内(FVIII 水平高达 200%),血栓形成风险的增加并不显著。血浆 FVIII 的延长升高并未进一步增加升高的 FVIII 水平的血栓形成潜力。