...
首页> 外文期刊>Molecular biology reports >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
【24h】

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

机译:内皮一氧化氮(eNOS)基因G894T和VNTR多态性与亚洲人缺血性中风发展的风险密切相关:流行病学研究的荟萃分析

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

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.
机译:尽管已经广泛研究了内皮型一氧化氮合酶(eNOS)基因多态性(包括G894T,VNTR和T786C)与缺血性中风(IS)的关系,但有争议的结果已有报道。这项研究的目的是通过荟萃分析来评估它们之间的关系。通过以下数据库检索文献:Medline,Embase和Wangfang(更新至2013年1月1日)。使用固定或随机效应模型来计算合并的优势比和95%的置信区间(OR和95%CI)。该荟萃分析最终纳入了总共31个病例对照研究,包括8,547例患者和9,117个对照。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发生风险增加显着相关(TT与GT + GG相比,OR和95%CI 1.25(1.09-1.42),P <0.001)。根据种族进行亚组分析时,亚洲人而非白种人的T等位基因与IS风险显着相关。对于eNOS VNTR多态性,与4bb基因型相比,4aa基因型与IS发生风险显着相关(aa与bb的OR(95%CI)2.22(1.66-2.97)比较,P <0.001)。同样,在进行亚组分析时,亚洲人而非白种人的4aa与IS风险增加密切相关。对于eNOS T786C多态性,它与IS发生风险无关。总之,这项研究表明,eNOS 894T和VNTR 4a等位基因与亚洲人IS发生风险显着相关。但是,eNOS T786C多态性不是IS发生的可能危险因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号