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缺血性卒中中基因多态性、环境因素及其相互作用的关联研究。

Association studies of genetic polymorphism, environmental factors and their interaction in ischemic stroke.

作者信息

Gao XuGuang, Yang Huo, ZhiPing Teng

机构信息

Department of Neurology, Peking University People's Hospital, 11 Xizhimen South St, Beijing, 100044, China.

出版信息

Neurosci Lett. 2006 May 8;398(3):172-7. doi: 10.1016/j.neulet.2005.12.078. Epub 2006 Jan 27.

Abstract

Genetic background plays an important role in susceptibility to ischemic stroke. Our aim was to investigate the association of genetic polymorphisms and ischemic stroke and to evaluate their interaction with environmental risk factors in the Chinese population. Angiotensin-converting enzyme (ACE) gene I/D polymorphism, apolipoprotein E (ApoE) gene polymorphism, methylenetetrahydrofolate reductase (MTHFR) gene 677C/T polymorphism, and beta fibrinogen (Fgbeta) gene 148C/T polymorphism were analyzed in 100 patients and 100 matched controls. The subjects were genotyped by polymerase chain reaction (PCR) amplification and denaturing high-performance liquid chromatography (DHPLC) analysis. Persons with the Fgbeta CT/TT, MTHFR CT/TT, and ACE ID/DD genotypes had an elevated incidence of ischemic stroke (OR 3.907, 95% CI, 1.160-13.162, P=0.028). Smokers with the Fgbeta CT/TT or APOEepsilon4epsilon3 genotype, as well as individuals with the Fgbeta CT/TT genotype who consumed alcohol were more likely to develop a stroke. The data indicate that certain unfavorable genotypic combinations act synergistically in the development of ischemic stroke in the Chinese population. Synergism was also observed between genotype and environmental risk factors. This study may facilitate the development of a strategy to effectively prevent ischemic strokes.

摘要

遗传背景在缺血性中风易感性中起重要作用。我们的目的是研究基因多态性与缺血性中风的关联,并评估它们与中国人群环境危险因素的相互作用。对100例患者和100例匹配对照进行血管紧张素转换酶(ACE)基因I/D多态性、载脂蛋白E(ApoE)基因多态性、亚甲基四氢叶酸还原酶(MTHFR)基因677C/T多态性和β纤维蛋白原(Fgbeta)基因148C/T多态性分析。通过聚合酶链反应(PCR)扩增和变性高效液相色谱(DHPLC)分析对受试者进行基因分型。Fgbeta CT/TT、MTHFR CT/TT和ACE ID/DD基因型的人缺血性中风发病率升高(OR 3.907,95%CI,1.160 - 13.162,P = 0.028)。具有Fgbeta CT/TT或APOEepsilon4epsilon3基因型的吸烟者,以及具有Fgbeta CT/TT基因型且饮酒的个体更易发生中风。数据表明,某些不利的基因型组合在中国人群缺血性中风发生中起协同作用。在基因型与环境危险因素之间也观察到协同作用。本研究可能有助于制定有效预防缺血性中风的策略。

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