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Folate Pathway Gene Methylenetetrahydrofolate Reductase C677T Polymorphism and Alzheimer Disease Risk in Asian Population

机译:叶酸途径基因亚甲基四氢叶酸还原酶C677T多态性与亚洲人群的阿尔茨海默氏病风险

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摘要

The association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and susceptibility to Alzheimers disease (AD) was controversial in previous studies. The present meta-analysis was designed to investigate the association of MTHFR C677T polymorphism with AD. Nine studies were identified by search of PubMed, Google Scholar, Elsevier, Springer Link databases, up to January 2013. Odds ratios (ORs) with corresponding 95 % confidence interval (CI) were calculated using fixed effects model or random effects model. All statistical analysis was done by Mix version 1.7. MTHFR C677T polymorphism had a significant association with susceptibility to AD in all genetic models (for T vs C: OR 1.29, 95 % CI 1.15–1.44, p < 0.0001; for TT + CT vs CC: OR 1.38, 95 % CI 1.16–1.364, p = 0.0002; for TT vs CC: OR 1.60, 95 % CI 1.25–2.04, p = 0.0001; for CT vs CC: OR 1.28, 95 % CI 1.1–1.53, p < 0.008; for TT vs CT + CC: OR 1.37, 95 % CI 1.12–1.67, p = 0.002). Results from present meta-analysis supported that the MTHFR C677T polymorphism was associated with an increased risk of AD in Asian population.
机译:在以前的研究中,亚甲基四氢叶酸还原酶(MTHFR)C677T多态性与阿尔茨海默氏病(AD)的易感性之间的关联存在争议。本荟萃分析旨在研究MTHFR C677T多态性与AD的关联。截至2013年1月,通过搜索PubMed,Google Scholar,Elsevier,Springer Link数据库确定了9项研究。使用固定效应模型或随机效应模型计算了具有95%置信区间(CI)的赔率(OR)。所有统计分析均由Mix版本1.7完成。在所有遗传模型中,MTHFR C677T多态性均与AD易感性密切相关(对于T vs C:OR 1.29,95%CI 1.15-1.44,p <0.0001;对于TT + CT vs CC:OR 1.38,95%CI 1.16– 1.364,p = 0.0002;对于TT vs CC:或1.60,95%CI 1.25–2.04,p = 0.0001;对于CT vs CC:或1.28,95%CI 1.1-1.53​​,p <0.008;对于TT vs CT + CC :OR 1.37,95%CI 1.12-1.67,p = 0.002)。目前的荟萃分析结果表明,MTHFR C677T多态性与亚洲人群罹患AD的风险增加有关。

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