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血小板糖蛋白Ia C807T基因多态性与冠状动脉疾病之间缺乏关联:一项荟萃分析。

Lack of association between the platelet glycoprotein Ia C807T gene polymorphism and coronary artery disease: a meta-analysis.

作者信息

Tsantes Argirios E, Nikolopoulos Georgios K, Bagos Pantelis G, Vaiopoulos Georgios, Travlou Anthi

机构信息

Laboratory of Hematology and Blood Bank Unit, Attikon General Hospital, School of Medicine, University of Athens, Athens, Greece.

出版信息

Int J Cardiol. 2007 May 31;118(2):189-96. doi: 10.1016/j.ijcard.2006.06.047. Epub 2006 Oct 3.

Abstract

BACKGROUND

The platelet-collagen receptor, glycoprotein (GP) la/lla plays a crucial role in the adhesion of platelets to fibrillar collagen, an event contributing to the pathogenesis of thrombosis. The C807T polymorphism of the GPla gene is considered a genetic marker of the platelet GPla/lla density. The importance of the GPla gene C807T polymorphism as a genetic risk factor for coronary artery disease (CAD) remains controversial. To assess this association, we performed a meta-analysis of published data.

METHODS

A comprehensive meta-analysis of 19 studies, with a total sample of 13835 subjects using random effects models.

RESULTS

The C versus T allele contrast gave an OR of 0.998 with 95% Cl 0.937-1.064. Similarly, comparing the C homozygotes with the T homozygotes, the CC genotype versus the others and the TT genotype versus the rest, no evidence of any gene-disease association was obtained. Furthermore, the meta-regression analysis did not disclose any variable that could modify the role of this polymorphism in the development of CAD.

CONCLUSION

Our findings support the view that C807T polymorphism of the GPla gene is not a significant risk factor for CAD, either alone or in combination with other major cardiovascular risk factors.

摘要

背景

血小板-胶原蛋白受体糖蛋白(GP)la/lla在血小板与纤维状胶原蛋白的黏附中起关键作用,这一过程与血栓形成的发病机制有关。GPla基因的C807T多态性被认为是血小板GPla/lla密度的遗传标志物。GPla基因C807T多态性作为冠状动脉疾病(CAD)遗传危险因素的重要性仍存在争议。为评估这种关联,我们对已发表的数据进行了荟萃分析。

方法

使用随机效应模型对19项研究进行全面荟萃分析,总样本量为13835名受试者。

结果

C等位基因与T等位基因的对比得出比值比(OR)为0.998,95%置信区间(CI)为0.937 - 1.064。同样,比较C纯合子与T纯合子、CC基因型与其他基因型以及TT基因型与其他基因型,未获得任何基因与疾病关联的证据。此外,荟萃回归分析未揭示任何可改变该多态性在CAD发生中作用的变量。

结论

我们的研究结果支持以下观点,即GPla基因的C807T多态性无论是单独还是与其他主要心血管危险因素联合,都不是CAD的显著危险因素。

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