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Genetic Polymorphisms Involved in Folate Metabolism and Maternal Risk for Down Syndrome: A Meta-Analysis

机译:遗传多态性涉及叶酸代谢和妊娠综合征的母体风险:荟萃分析

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Inconclusive results of the association between genetic polymorphisms involved in folate metabolism and maternal risk for Down syndrome (DS) have been reported. Therefore, this meta-analysis was conducted. We searched electronic databases through May, 2014, for eligible studies. Pooled odds ratios with 95% confidence intervals were used to assess the strength of the association, which was estimated by fixed or random effects models. Heterogeneity among studies was evaluated using Q-test and I 2 statistic. Subgroup and sensitivity analyses were also conducted. Publication bias was estimated using Begg's and Egger's tests. A total of 17 case-controls studies were included. There was evidence for an association between the MTRR c.66AG (rs1801394) polymorphism and maternal risk for DS. In the subgroup analysis, increased maternal risk for DS was found in Caucasians. Additionally, the polymorphic heterozygote MTHFD1 1958GA genotype was associated significantly with maternal risk for DS, when we limit the analysis by studies conformed to Hardy-Weinberg equilibrium. Finally, considering MTR c.2756AG (rs1805087), TC2 c.776CG (rs1801198), and CBS c.844ins68, no significant associations have been found, neither in the overall analyses nor in the stratified analyses by ethnicity. In conclusion, our meta-analysis suggested that the MTRR c.66AG(rs1801394) polymorphismand MTHFD1 c.1958GA (rs2236225) were associated with increased maternal risk for DS.
机译:据报道,叶酸代谢遗传多态性与衰减综合征(DS)中涉及的遗传多态性相关性的不确定结果。因此,进行了该荟萃分析。我们于2014年5月搜索了电子数据库,以便合格研究。汇集了95%置信区间的差异比率来评估关联的强度,由固定或随机效应模型估算。使用Q-Test和I 2统计来评估研究中的异质性。还进行了亚组和敏感性分析。使用BEGG和EGGER的测试估计出版物偏见。共有17项病例对照研究。 MTRR C.66A> G(RS1801394)多态性和DS的母体风险之间存在证据。在亚组分析中,在高加索人中发现了DS的母体风险增加。另外,当我们通过研究符合Hardy-Weinberg均衡的研究来限制分析时,多晶族杂合子MTHFD1 1958GA基因型与DS的母体风险显着相关。最后,考虑到MTR C.2756A> G(RS1805087),TC2 C.776C> G(RS1801198)和CBS C.844INS68,没有发现重大关联,既不在整体分析中也没有通过种族分析分析。总之,我们的Meta分析表明,MTRR C.66A> G(RS1801394)多态性和MTHFD1 C.1958G> a(rs2236225)与DS的母体风险增加有关。

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