Allaart C F, Aronson D C, Ruys T, Rosendaal F R, van Bockel J H, Bertina R M, Briët E
Haemostasis and Thrombosis Research Unit, University Hospital Leiden, The Netherlands.
Thromb Haemost. 1990 Oct 22;64(2):206-10.
Protein S is the vitamin K dependent cofactor of activated protein C. It has an important role in the regulation of blood coagulation and fibrinolysis. Hereditary protein S deficiency is associated with familial venous thrombophilia. Since a few patients with arterial occlusions have been reported to be protein S deficient, it is speculated that hereditary protein S deficiency may be also a risk factor for the development of arterial thrombosis. In a group of 37 consecutive patients with arterial occlusive disease presenting before the age of 45, three patients were found heterozygous for hereditary protein S deficiency. None of the patients had a protein C deficiency or an antithrombin III deficiency. Family investigations showed a clear association between the hereditary deficiency and venous thrombosis, but a relation between the deficiency and arterial thrombosis was less obvious. A review of previous literature on patients with arterial thrombosis and protein S deficiency revealed that more extensive studies are needed to demonstrate whether or not hereditary protein S deficiency is a risk factor for the development of arterial thrombosis.
蛋白S是活化蛋白C的维生素K依赖性辅助因子。它在血液凝固和纤维蛋白溶解的调节中起重要作用。遗传性蛋白S缺乏与家族性静脉血栓形成倾向有关。由于有报道称少数动脉闭塞患者存在蛋白S缺乏,因此推测遗传性蛋白S缺乏可能也是动脉血栓形成的危险因素。在一组连续37例45岁以前出现动脉闭塞性疾病的患者中,发现3例患者为遗传性蛋白S缺乏杂合子。所有患者均无蛋白C缺乏或抗凝血酶III缺乏。家族调查显示遗传性缺乏与静脉血栓形成之间存在明显关联,但缺乏与动脉血栓形成之间的关系不太明显。对先前有关动脉血栓形成和蛋白S缺乏患者的文献进行回顾发现,需要更广泛的研究来证明遗传性蛋白S缺乏是否是动脉血栓形成的危险因素。