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与静脉和动脉血栓栓塞易感性相关的基因多态性:健康德国人群中的频率分布

Gene polymorphisms implicated in influencing susceptibility to venous and arterial thromboembolism: frequency distribution in a healthy German population.

作者信息

Hoppe Berthold, Tolou Farzaneh, Dörner Thomas, Kiesewetter Holger, Salama Abdulgabar

机构信息

Institute of Transfusion Medicine, Campus Benjamin Franklin, Charité - Universitätsklinikum Berlin, Berlin, Germany.

出版信息

Thromb Haemost. 2006 Oct;96(4):465-70.

Abstract

Evolvement and progression of cardiovascular diseases affecting the venous and arterial system are influenced by a multitude of environmental and hereditary factors. Many of these hereditary factors consist of defined gene polymorphisms, such as single nucleotide polymorphisms (SNPs) or insertion-deletion polymorphisms, which directly or indirectly affect the hemostatic system. The frequencies of individual hemostatic gene polymorphisms in different normal populations are well defined. However, descriptions of patterns of genetic variability of a larger extent of different factors of hereditary hypercoagulability in single populations are scarce. The aim of this study was i) to give a detailed description of the frequencies of factors of hereditary thrombophilia and their combinations in a German population (n = 282) and ii) to compare their distributions with those reported for other regions. Variants of coagulation factors [factor V 1691G>A (factor V Leiden), factor V 4070A>G (factor V HR2 haplotype), factor VII Arg353Gln, factor XIII Val34Leu, beta-fibrinogen -455G>A, prothrombin 20210G>A], coagulation inhibitors [tissue factor pathway inhibitor 536C>T, thrombomodulin 127G>A], fibrinolytic factors [angiotensin converting enzyme intron 16 insertion/deletion, factor VII-activating protease 1601G>A (FSAP Marburg I), plasminogen activator inhibitor 1-675 insertion/deletion (5G/4G), tissue plasminogen activator intron h deletion/insertion], and other factors implicated in influencing susceptibility to thromboembolic diseases [apolipoprotein E2/E3/E4, glycoprotein Ia 807C>T, methylenetetrahydrofolate reductase 677C>T] were included. The distribution of glycoprotein Ia 807C>T deviated significantly from the Hardy-Weinberg equilibrium, and a comparison with previously published data indicates marked region and ethnicity dependent differences in the genotype distributions of some other factors.

摘要

影响静脉和动脉系统的心血管疾病的演变和进展受到多种环境和遗传因素的影响。其中许多遗传因素由特定的基因多态性组成,如单核苷酸多态性(SNP)或插入缺失多态性,它们直接或间接影响止血系统。不同正常人群中个体止血基因多态性的频率已得到明确界定。然而,关于单个人群中更大范围的遗传性高凝因素不同因素的遗传变异模式的描述却很少。本研究的目的是:i)详细描述德国人群(n = 282)中遗传性血栓形成因素及其组合的频率;ii)将它们的分布与其他地区报告的分布进行比较。纳入了凝血因子[因子V 1691G>A(因子V莱顿)、因子V 4070A>G(因子V HR2单倍型)、因子VII Arg353Gln、因子XIII Val34Leu、β-纤维蛋白原 -455G>A、凝血酶原20210G>A]、凝血抑制剂[组织因子途径抑制剂536C>T、血栓调节蛋白127G>A]、纤维蛋白溶解因子[血管紧张素转换酶内含子16插入/缺失、因子VII激活蛋白酶1601G>A(FSAP马尔堡I)、纤溶酶原激活物抑制剂1 - 675插入/缺失(5G/4G)、组织纤溶酶原激活物内含子h缺失/插入]以及其他与血栓栓塞性疾病易感性相关的因素[载脂蛋白E2/E3/E4、糖蛋白Ia 807C>T、亚甲基四氢叶酸还原酶677C>T]。糖蛋白Ia 807C>T的分布显著偏离哈迪-温伯格平衡,与先前发表的数据比较表明,其他一些因素的基因型分布存在明显的地区和种族依赖性差异。

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