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尼日利亚人和欧洲人的血小板功能、凝血因子VIII、纤维蛋白原及纤维蛋白溶解与动脉粥样硬化和血栓形成的关系

Platelet function, factor VIII, fibrinogen, and fibrinolysis in Nigerians and Europeans in relation to atheroma and thrombosis.

作者信息

Dupuy E, Fleming A F, Caen J P

出版信息

J Clin Pathol. 1978 Nov;31(11):1094-101. doi: 10.1136/jcp.31.11.1094.

Abstract

Platelet function, factor VIII, fibrinogen levels, and fibrinolysis were studied in Europeans and in two groups of Nigerians living in Zaria, northern Nigeria, in order to see whether differences could help to explain the low incidence of atheroma and thrombosis in Nigerians. We confirmed the relative thrombocytopenia and observed a rapid disaggregation after ADP-induced platelet aggregation in Nigerians. The most striking difference was a reduced or absent ristocetin-induced platelet aggregation in Nigerian platelet-rich plasma, probably due to a plasma component interacting with the von Willebrand activity (VWF), since factor VIII coagulant activity, factor VIII related antigen, and isolated VWF were normal or high by European standards. Group II (rural population), but not group I (senior university staff in Zaria) of the Nigerians, tended to have high serum fibrinogen concentrations. Spontaneous fibrinolytic activity was enhanced in most Nigerians compared to the Europeans and was normally increased after venostasis in proportion to the initial activity. Fibrinolysis and ristocetin-induced platelet aggregation values for the Nigerians in group I were intermediate between European and Nigerian in the group II values, suggesting that differences were due more to environmental than to genetic factors.Relative thrombocytopenia, disaggregation after ADP-induced aggregation, inhibition of ristocetin-induced platelet aggregation, and active fibrinolysis help to explain the infrequency of thrombotic disease in Africans. Also the low incidence of atheroma may follow from less platelet adherence and less platelet release of mitogenic factors, which cause intimal hyperplasia.

摘要

对欧洲人以及居住在尼日利亚北部扎里亚的两组尼日利亚人进行了血小板功能、凝血因子VIII、纤维蛋白原水平和纤维蛋白溶解的研究,以探讨这些差异是否有助于解释尼日利亚人动脉粥样硬化和血栓形成发病率较低的原因。我们证实了尼日利亚人存在相对血小板减少症,并观察到二磷酸腺苷(ADP)诱导的血小板聚集后迅速解聚。最显著的差异是尼日利亚富含血小板血浆中瑞斯托霉素诱导的血小板聚集减少或缺乏,这可能是由于血浆成分与血管性血友病因子活性(VWF)相互作用所致,因为按照欧洲标准,凝血因子VIII促凝活性、凝血因子VIII相关抗原和分离的VWF均正常或偏高。尼日利亚人第二组(农村人口)而非第一组(扎里亚的大学高级职员)血清纤维蛋白原浓度往往较高。与欧洲人相比,大多数尼日利亚人的自发纤维蛋白溶解活性增强,并且在静脉淤血后通常会根据初始活性成比例增加。第一组尼日利亚人的纤维蛋白溶解和瑞斯托霉素诱导的血小板聚集值介于欧洲人和第二组尼日利亚人之间,这表明差异更多是由环境因素而非遗传因素导致的。相对血小板减少症、ADP诱导聚集后的解聚、瑞斯托霉素诱导血小板聚集的抑制以及活跃的纤维蛋白溶解有助于解释非洲人血栓性疾病发生率较低的原因。此外,动脉粥样硬化发病率较低可能是由于血小板黏附减少以及促有丝分裂因子的血小板释放减少,而促有丝分裂因子会导致内膜增生。

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