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Association between SNP12 in estrogen receptor α gene and hypospadias: a systematic review and meta-analysis

机译:雌激素受体α基因中SNP12与尿道下裂的关联:系统评价和Meta分析

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摘要

To investigate the association between single nucleotide polymorphism 12 in estrogen receptor α gene and hypospadias, four databases (PubMed, Web of Science, Embase and Cochrane Library) were electronically searched by 2nd November 2015. Finally, four studies were included for our meta-analysis, involving 1379 cases and 1648 controls. A quality assessment was performed using the Newcastle–Ottawa Scale of case–control study. Meta-analysis and publication bias measuring were all done by Stata 12.0. No significant publication bias (PBegg = 0.296, PEgger = 0.161) was found. Overall, there was statistically significant association for recessive genetic model (AA vs. GA + GG: OR 3.45, 95 % CI [1.89, 6.30], P = 0.038). Moreover, the positive result was confirmed using trial sequential analysis even only three original studies. For allele model, there was also statistically significant association (allele A vs. G: OR 1.43, 95 % CI [1.23, 1.67], P = 0.034). Meanwhile, A allele as a risk factor turned out to be true positive by trial sequential analysis. In a word, this meta-analysis suggested that the single nucleotide polymorphism 12 definitely increase the risk of hypospadias.
机译:为了研究雌激素受体α基因中的单核苷酸多态性12与尿道下裂之间的关联,在2015年11月2日之前以电子方式搜索了四个数据库(PubMed,Web of Science,Embase和Cochrane Library)。最后,我们纳入了四项研究作为荟萃分析,涉及1379例病例和1648例对照。使用病例对照研究的纽卡斯尔-渥太华量表进行了质量评估。荟萃分析和出版偏倚测量均由Stata 12.0完成。未发现明显的出版偏倚(PBegg = 0.296,PEgger = 0.161)。总体而言,隐性遗传模型具有统计学上的显着关联(AA vs.GA + GG:OR 3.45,95%CI [1.89,6.30],P = 0.038)。此外,即使仅进行了三项原始研究,仍通过试验性顺序分析证实了阳性结果。对于等位基因模型,也存在统计学上的显着相关性(等位基因A与G:OR 1.43,95%CI [1.23,1.67],P = 0.034)。同时,通过试验序贯分析,等位基因作为危险因素被证明是真实阳性。总之,这项荟萃分析表明单核苷酸多态性12无疑会增加尿道下裂的风险。

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