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Methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and risk of preeclampsia: An updated meta-analysis based on 51 studies

机译:亚甲基四氢叶酸还原酶(MTHFR)基因C677T多态性与先兆子痫的风险:基于51个研究的最新荟萃分析

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Background and Aims: The methylenetetrahydrofolate reductase (. MTHFR) gene C677T polymorphism has been considered to be associated with preeclampsia (PE), but the results from previous studies were conflicting. The present study aimed at investigating the frequency of preeclampsia according to the distribution polymorphism using a meta-analysis on the published studies. Methods: The English and Chinese databases were searched to identify eligible studies published in English before August 2012. Data were extracted using standardized methods. The association was assessed by odds ratio (OR) with 95% confidence intervals (CI). Begg's test was used to measure publication bias. Results: A total of 51 case-control studies containing 6,403 patients and 11,346 controls were involved in this meta-analysis. Significant associations were detected between MTHFR C677T polymorphism and risk of PE in the overall population for TT vs. CC (OR = 1.280, 95% CI: 1.074-1.525), recessive model (OR = 1.264, 95% CI: 1.067-1.303), and dominant genetic model (OR = 1.174, 95% CI: 1.057-1.303); in Caucasian population for dominant model (OR = 1.136, 95% CI: 1.022-1.263), and in East Asia population for TT vs. CC (OR = 2.199, 95% CI: 1.366-3.924) CT vs. CC (OR = 1.453, 95% CI: 1.001-2.109), recessive model (OR = 1.742, 95% CI: 1.202-2.525), and dominant model (OR = 1.783, 95% CI: 1.271-2.501). Conversely, no associations were detected in Latin America, South Asia, and Africa populations. Conclusions: Results of the meta-analysis suggest that the MTHFR C677T polymorphism was associated with risk of PE in overall, Caucasian, and East Asia populations. Nevertheless, the results for Latino, East Asians, South Asians and Africans should be interpreted with caution due to the small sample size.
机译:背景与目的:亚甲基四氢叶酸还原酶(。MTHFR)基因C677T多态性被认为与先兆子痫(PE)相关,但先前的研究结果相互矛盾。本研究旨在通过对已发表研究的荟萃分析,根据子代分布的多态性调查先兆子痫的发生频率。方法:检索英语和中文数据库,以鉴定2012年8月之前以英语发表的合格研究。采用标准化方法提取数据。通过比值比(OR)和95%置信区间(CI)评估关联。贝格检验用于衡量出版偏倚。结果:这项荟萃分析共涉及51个病例对照研究,包括6,403名患者和11,346名对照。在TT与CC(OR = 1.280,95%CI:1.074-1.525),隐性模型(OR = 1.264,95%CI:1.067-1.303)中,MTHFR C677T多态性与总人群PE风险之间存在显着关联。 ,以及优势遗传模型(OR = 1.174,95%CI:1.057-1.303);占主导地位模型的白种人人群(OR = 1.136,95%CI:1.022-1.263),在东亚人口中TT vs. CC(OR = 2.199,95%CI:1.366-3.924)CT vs. CC(OR = 1.453、95%CI:1.001-2.109),隐性模型(OR = 1.742,95%CI:1.22-2.525)和显性模型(OR = 1.783,95%CI:1.27-12-501)。相反,在拉丁美洲,南亚和非洲人口中未发现任何关联。结论:荟萃分析的结果表明,MTHFR C677T多态性与总体,白种人和东亚人群的PE风险有关。尽管如此,由于样本量较小,对拉丁裔,东亚人,南亚人和非洲人的结果应谨慎解释。

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