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凝血酶原基因20210A等位基因的共同遗传增加了家族性血栓形成倾向患者发生血栓形成的风险。

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia.

作者信息

Makris M, Preston F E, Beauchamp N J, Cooper P C, Daly M E, Hampton K K, Bayliss P, Peake I R, Miller G J

机构信息

University of Sheffield, Royal Hallamshire Hospital, Department of Medicine and Pharmacology, UK.

出版信息

Thromb Haemost. 1997 Dec;78(6):1426-9.

PMID:9423788
Abstract

The presence of the 20210A allele of the prothrombin (PT) gene has recently been shown to be a risk factor for venous thromboembolism. This is probably mediated through increased plasma prothrombin levels. The aim of this study was to compare the prevalence of the prothrombin 20210A allele in control subjects and in subjects with recognised thrombophilia and to establish whether the additional inheritance of the PT 20210A allele is associated with an increased risk of venous thromboembolism. 101 subjects with a history of venous thromboembolism and diagnosed as having either factor V Leiden (R506Q) or heritable deficiencies of protein C, protein S or antithrombin were studied. The prevalence of the PT 20210A allele in this group was compared with the results obtained for 150 control subjects. In addition, the relationships were examined between genetic status and the number of documented thromboembolic episodes, and between plasma prothrombin levels and possession of the PT 20210A allele. 8 (7.9%) of the 101 patients were also heterozygous for the PT 20210A allele. This compares with 0.7% in the control subjects (p = 0.005). After exclusion of patients on warfarin, the mean plasma prothrombin of 113 subjects without 20210A was 1.09 U/ml, as compared with 1.32 U/ml in 8 with the allele (p = 0.0002). Among the 101 patients with either factor V Leiden, protein S deficiency, protein C deficiency or antithrombin deficiency, the age adjusted mean (SD) number of venous thromboembolic episodes at diagnosis was 3.7 (1.5) in those with the PT 20210A allele, as compared with 1.9 (1.1) in those without (p = 0.0001). We have demonstrated that the prevalence of the PT 20210A allele is significantly greater in subjects with venous thrombosis and characterised heritable thrombophilia than in normal control subjects and that the additional inheritance of PT 20210A is associated with an increased risk of venous thromboembolism. We have also confirmed that plasma prothrombin levels are significantly greater in subjects possessing the PT 20210A compared with those who do not.

摘要

凝血酶原(PT)基因20210A等位基因的存在最近已被证明是静脉血栓栓塞的一个危险因素。这可能是通过血浆凝血酶原水平升高介导的。本研究的目的是比较对照组和已确诊有血栓形成倾向的受试者中凝血酶原20210A等位基因的患病率,并确定PT 20210A等位基因的额外遗传是否与静脉血栓栓塞风险增加相关。对101名有静脉血栓栓塞病史且被诊断为患有因子V莱顿突变(R506Q)或遗传性蛋白C、蛋白S或抗凝血酶缺乏症的受试者进行了研究。将该组中PT 20210A等位基因的患病率与150名对照受试者的结果进行了比较。此外,还研究了基因状态与记录的血栓栓塞发作次数之间的关系,以及血浆凝血酶原水平与PT 20210A等位基因携带情况之间的关系。101名患者中有8名(7.9%)也是PT 20210A等位基因的杂合子。而对照受试者中的这一比例为0.7%(p = 0.005)。在排除服用华法林的患者后,113名没有20210A等位基因的受试者的平均血浆凝血酶原为1.09 U/ml,而8名携带该等位基因的受试者的平均血浆凝血酶原为1.32 U/ml(p = 0.0002)。在101名患有因子V莱顿突变、蛋白S缺乏、蛋白C缺乏或抗凝血酶缺乏的患者中,诊断时年龄校正后的静脉血栓栓塞发作平均次数(标准差)在携带PT 20210A等位基因的患者中为3.7(1.5),而在未携带该等位基因的患者中为1.9(1.1)(p = 0.0001)。我们已经证明,静脉血栓形成且具有特征性遗传性血栓形成倾向的受试者中PT 20210A等位基因的患病率显著高于正常对照受试者,并且PT 20210A的额外遗传与静脉血栓栓塞风险增加相关。我们还证实,携带PT 20210A的受试者的血浆凝血酶原水平显著高于未携带该等位基因的受试者。

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