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Endothelial nitric oxide synthase gene polymorphisms and risk of preeclampsia

机译:内皮型一氧化氮合酶基因多态性与先兆子痫的风险

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摘要

Polymorphisms in endothelial nitric oxide synthase (eNOS) gene may affect the risk of preeclampsia. This systematic review aimed to provide an updated review of the literature to better understand the association between the eNOS gene polymorphisms and the risk of preeclampsia. We searched electronic databases of the human literature in PubMed, EMBASE, and the Cochrane Library up to July 2012. A meta-analysis was conducted on the association of eNOS G894T, T786C, and intron 4b/a polymorphisms with preeclampsia using (1) allele contrast, (2) recessive, (3) dominant, and (4) additive models. Thirty-three studies comprising 10,671 participants met the inclusion criteria. There was statistically significant association between the G894T variant and increased risk of preeclampsia (TT versus TG + GG: odds ratio 1.43, 95% confidence interval: 1.13 to 1.82). However, no significant risk of preeclampsia was observed either in the T786C or the intron 4b/a polymorphism. Homozygosity TT in eNOS G894T variant is significantly associated with an increased risk of preeclampsia.
机译:内皮型一氧化氮合酶(eNOS)基因的多态性可能会影响先兆子痫的风险。该系统综述旨在提供文献的最新综述,以更好地了解eNOS基因多态性与先兆子痫风险之间的关系。我们检索了截至2012年7月在PubMed,EMBASE和Cochrane图书馆中的人类文献电子数据库。使用(1)等位基因对eNOS G894T,T786C和内含子4b / a多态性与先兆子痫的关联进行了荟萃分析。相反,(2)隐性模型,(3)显性模型和(4)加性模型。共有10,671名参与者的33项研究符合纳入标准。 G894T变体与先兆子痫风险增加之间存在统计学上的显着相关性(TT与TG + GG:优势比1.43,95%置信区间:1.13至1.82)。但是,在T786C或内含子4b / a多态性中均未观察到子痫前期的显着风险。 eNOS G894T变异体的纯合性TT与子痫前期风险增加显着相关。

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