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Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and susceptibility to ischemic stroke: A meta-analysis

机译:亚甲基四氢叶酸还原酶(MTHFR)基因多态性与缺血性中风的易感性:荟萃分析

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摘要

Associations between 5,10-methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and ischemic stroke have been reported (Ariyaratnam et al., 2007; Banerjee et al., 2007; Casas et al., 2004), but the results of these studies are inconsistent. To investigate the possible associations between the MTHFR gene polymorphism and ischemic stroke, we performed a meta-analysis. Nineteen case-control studies associated with MTHFR gene C667T involving 2223 cases and 2936 controls were included. Heterogeneity among studies was evaluated with I2 and Egger's test and an inverted funnel plot was used to assess publication bias. Odds ratio (OR) was observed to identify the associations. Statistically significant association with ischemic stroke was identified for allele T polymorphism of MTHFR [fixed-effects OR=1.28, 95% confidence interval (95% CI): 1.17-1.40, P0.00001] and marginally significant association was detected with genotype CT of MTHFR (fixed-effects OR=1.13, 95% CI: 1.01-127, P=0.04) and genotype TT of MTHFR (fixed-effects OR=1.43, 95% CI: 1.20-1.70, P0.001). The results suggested that the MTHFR C667T genetic polymorphism was significantly associated with increased risk of ischemic stroke.
机译:已经报道了5,10-亚甲基四氢叶酸还原酶(MTHFR)基因C677T多态性与缺血性中风之间的关联(Ariyaratnam等,2007; Banerjee等,2007; Casas等,2004),但这些研究的结果是不一致。为了研究MTHFR基因多态性与缺血性卒中之间的可能关联,我们进行了荟萃分析。涉及19个与MTHFR基因C667T相关的病例对照研究,涉及2223例病例和2936例对照。使用I2和Egger检验评估研究之间的异质性,并使用倒漏斗图评估出版偏倚。观察到赔率(OR)可以识别这种关联。 MTHFR的等位基因T多态性与缺血性卒中有统计学意义的相关性[固定效应OR = 1.28,95%的置信区间(95%CI):1.17-1.40,P <0.00001],并且与基因型CT的边际显着相关MTHFR(固定效应OR = 1.13,95%CI:1.01-127,P = 0.04)和MTHFR的基因型TT(固定效应OR = 1.43,95%CI:1.20-1.70,P <0.001)。结果表明,MTHFR C667T基因多态性与缺血性中风的风险增加显着相关。

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