节点文献
MTHFR基因C677T纯合突变与偏头痛发病风险的meta分析
Association between homozygous C677T mutation in MTHFR gene and migraine:a meta-analysis
【摘要】 目的:探讨MTHFR基因C677T纯合突变与偏头痛的相关性。方法:应用RevMan 5.0软件对20000年1月到2013年12月之间发表的有关MTHFR基因C677T多态性与偏头痛相关性的22项相关研究的文献进行了荟萃分析,共纳入8622例偏头痛患者,28376例对照。结果:随机效应模型分析结果显示,TT基因型能增加先兆型偏头痛发病风险,OR 1.45[95%CI,1.10~1.92];但不能增加无先兆偏头痛发病风险,OR 1.01[95%CI,0.91~1.13]。结论:MTHFR基因C677T纯合突变与先兆型偏头痛相关,与无先兆偏头痛无明确相关。TT基因型能增加先兆型偏头痛发病风险。
【Abstract】 Objective:To investigate the association between the homozygous C677 T mutation in MTHFR gene and migraine.Methods:We performed a meta-analysis of 22 studies comprising 8622 cases and 28376 control subjects investigating the MTHFR C677 T polymorphisms by using the RevMan version 5.0 software.Results:An overall random-effect odds ratio of 1.45(95%confidence interval,1.10 to 1.92) was found for TT genotype in migraine with aura,but not in migraine without aura(odds ratio,1.01,95%confidence interval,0.91 to 1.13).Conclusion:The homozygous C677 T mutation in MTHFR gene is associated with migraine with aura,but not in migraine without aura.There is an increased risk of migraine with aura associated with the TT genotype.
【Key words】 Methylenetetrahydrofolate reductase; C677T; migraine; meta-analysis;
- 【文献出处】 广州医学院学报 ,Academic Journal of Guangzhou Medical College , 编辑部邮箱 ,2014年02期
- 【分类号】R747.2
- 【下载频次】4