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阵发性夜间血红蛋白尿中的活化血小板。

Activated platelets in paroxysmal nocturnal haemoglobinuria.

作者信息

Gralnick H R, Vail M, McKeown L P, Merryman P, Wilson O, Chu I, Kimball J

机构信息

Hematology Service, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Br J Haematol. 1995 Nov;91(3):697-702. doi: 10.1111/j.1365-2141.1995.tb05371.x.

Abstract

One of the major causes of morbidity and mortality in paroxysmal nocturnal haemoglobinuria (PNH) is venous thrombosis. We have studied fibrinolysis, coagulation and platelets in 11 patients with PNH in an attempt to identify the possible mechanism(s) of thrombosis in PNH. In this study we did not identify any fibrinolytic defects, evidence of coagulation activation, nor reduction in coagulation inhibitors. In contrast, in this cohort of 11 PNH patients we have identified varying degrees of platelet activation as defined by the surface expression of activation-dependent proteins and the binding of adhesive proteins to the platelet surface. The thrombotic events in PNH usually occur in the venous system. Our studies and previous experimental studies suggest that anti-platelet therapy may be efficacious in reducing the incidence and severity of venous thrombosis in PNH.

摘要

阵发性夜间血红蛋白尿(PNH)发病和死亡的主要原因之一是静脉血栓形成。我们研究了11例PNH患者的纤溶、凝血和血小板情况,试图确定PNH血栓形成的可能机制。在本研究中,我们未发现任何纤溶缺陷、凝血激活证据或凝血抑制剂减少。相反,在这11例PNH患者队列中,我们发现了不同程度的血小板激活,这是由激活依赖性蛋白的表面表达以及黏附蛋白与血小板表面的结合所定义的。PNH中的血栓事件通常发生在静脉系统。我们的研究及之前的实验研究表明,抗血小板治疗可能有效降低PNH患者静脉血栓形成的发生率和严重程度。

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