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内皮型一氧化氮合酶(eNOS)基因G894T和可变数目串联重复序列(VNTR)多态性与亚洲人发生缺血性中风的风险密切相关:流行病学研究的荟萃分析

Endothelial nitric oxide (eNOS) gene G894T and VNTR polymorphisms are closely associated with the risk of ischemic stroke development for Asians: meta-analysis of epidemiological studies.

作者信息

Guo Xiaolong

机构信息

Department of Neurosurgery, The First Affiliated Hospital of Henan University of Science and Technology, Jinghua Road No. 24, Jianxi, Luoyang, Henan, People's Republic of China,

出版信息

Mol Biol Rep. 2014;41(4):2571-83. doi: 10.1007/s11033-014-3115-8. Epub 2014 Feb 27.

Abstract

Although the relationships between endothelial nitric oxide synthase (eNOS) gene polymorphisms (including G894T, VNTR and T786C) and risk of ischemic stroke (IS) have been extensively studied, controversial results have been reported. The aim of this study was to assess the relationships between them by using a meta-analysis. Literatures were retrieved through the following databases: Medline, Embase and Wangfang (updated to January 1st, 2013). Fixed- or random-effects model was used to calculate pooled odds ratio and 95 % confidence interval (OR and 95 % CI). A total of 31 case-control studies including 8,547 patients and 9,117 controls were included in this meta-analysis eventually. For eNOS G894T polymorphism, the results indicated that TT genotype was significantly associated with increased risk of IS incidence compared to G allele (OR and 95 % CI 1.25 (1.09-1.42) for TT vs. GT+GG, P < 0.001). When subgroup analysis was conducted according to ethnicities, T allele was significantly associated with risk of IS for Asians rather than for Caucasians. For eNOS VNTR polymorphism, 4aa genotype was significantly associated with risk of IS incidence compared to 4bb genotype (OR (95 % CI) 2.22 (1.66-2.97) for aa vs. bb, P < 0.001). Similarly, when subgroup analyses were conducted, 4aa was closely associated with increased risk of IS for Asians rather than for Caucasians. For eNOS T786C polymorphism, it was not associated with risk of IS incidence. In conclusion, this study indicated that eNOS 894T and VNTR 4a allele was significantly associated with risk of IS incidence for Asians. However, eNOS T786C polymorphism was not a likely risk factor for IS incidence.

摘要

尽管内皮型一氧化氮合酶(eNOS)基因多态性(包括G894T、可变数目串联重复序列(VNTR)和T786C)与缺血性脑卒中(IS)风险之间的关系已得到广泛研究,但仍有相互矛盾的结果报道。本研究的目的是通过荟萃分析评估它们之间的关系。通过以下数据库检索文献:医学文献数据库(Medline)、荷兰医学文摘数据库(Embase)和万方数据库(更新至2013年1月1日)。采用固定效应或随机效应模型计算合并比值比和95%置信区间(OR和95%CI)。最终,本荟萃分析纳入了31项病例对照研究,包括8547例患者和9117例对照。对于eNOS G894T多态性,结果表明,与G等位基因相比,TT基因型与IS发病风险增加显著相关(TT与GT+GG相比,OR和95%CI为1.25(1.09 - 1.42),P < 0.001)。按种族进行亚组分析时,T等位基因与亚洲人的IS风险显著相关,而与高加索人无关。对于eNOS VNTR多态性,与4bb基因型相比,4aa基因型与IS发病风险显著相关(aa与bb相比,OR(95%CI)为2.22(1.66 - 2.97),P < 0.001)。同样,进行亚组分析时,4aa与亚洲人的IS风险增加密切相关,而与高加索人无关。对于eNOS T786C多态性,它与IS发病风险无关。总之,本研究表明,eNOS 894T和VNTR 4a等位基因与亚洲人的IS发病风险显著相关。然而,eNOS T786C多态性不太可能是IS发病的危险因素。

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