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亚甲基四氢叶酸还原酶(MTHFR)C677T基因多态性会增加患阿尔茨海默病的风险:基于40项病例对照研究的证据。

The MTHFR C677T polymorphism contributes to increased risk of Alzheimer's disease: evidence based on 40 case-control studies.

作者信息

Peng Qiliu, Lao Xianjun, Huang Xiuli, Qin Xue, Li Shan, Zeng Zhiyu

机构信息

Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

Department of Geriatrics, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

出版信息

Neurosci Lett. 2015 Jan 23;586:36-42. doi: 10.1016/j.neulet.2014.11.049. Epub 2014 Dec 5.

Abstract

The association between methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and Alzheimer's Disease (AD) risk has been widely reported with inconsistent results. We performed an updated meta-analysis of all available studies to clarify this situation. We conducted a comprehensive literature search in PubMed Alzgene, Embase, and Chinese Biomedical Literature database (CBM) for the period up to June 2014. Finally, a total of 40 case-control studies with 4503 AD cases and 5767 controls were included. Overall, significant increased AD risk was found, when all studies were pooled into the meta-analysis. In subgroup analyses stratified by ethnicity, age of onset, and APOE ϵ4 status, significant increased AD risk was found in Asians, late-onset AD, and APOE ϵ4 carriers, but not in Caucasians, early-onset AD, and non-APOE ϵ4 carriers. The present meta-analysis suggested that the MTHFR is a candidate gene for AD susceptibility. The MTHFR C677T polymorphism may be a risk factor for AD in Asians, APOE ϵ4 carriers, and late-onset AD. Further, investigations taking the potential gene-gene and gene-environmental interactions into consideration for the MTHFR C677T polymorphism should be conducted.

摘要

亚甲基四氢叶酸还原酶(MTHFR)基因C677T多态性与阿尔茨海默病(AD)风险之间的关联已有广泛报道,但结果并不一致。我们进行了一项更新的荟萃分析,纳入所有可得研究以阐明这一情况。我们在PubMed、Alzgene、Embase和中国生物医学文献数据库(CBM)中进行了全面的文献检索,检索时间截至2014年6月。最终,共纳入40项病例对照研究,其中AD病例4503例,对照5767例。总体而言,当将所有研究纳入荟萃分析时,发现AD风险显著增加。在按种族、发病年龄和APOE ε4状态分层的亚组分析中,发现亚洲人、晚发型AD和APOE ε4携带者的AD风险显著增加,但在高加索人、早发型AD和非APOE ε4携带者中未发现。本荟萃分析表明,MTHFR是AD易感性的一个候选基因。MTHFR C677T多态性可能是亚洲人、APOE ε4携带者和晚发型AD患AD的一个风险因素。此外,应开展进一步研究,考虑MTHFR C677T多态性潜在的基因-基因和基因-环境相互作用。

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