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亚甲基四氢叶酸还原酶基因C677T多态性与晚发性阿尔茨海默病易感性

The C677T Polymorphism of the Methylenetetrahydrofolate Reductase Gene and Susceptibility to Late-onset Alzheimer's Disease.

作者信息

Yi Jian, Xiao Lan, Zhou Sheng-Qiang, Zhang Wen-Jiang, Liu Bai-Yan

机构信息

Key Laboratory of Internal Medicine, The Frist Hospital Hunan University of Traditional Chinese Medicine, Changsha 410007, Hunan Province, P.R. China.

Hunan University of Traditional Chinese Medicine, Changsha 410208, Hunan Province, P.R. China.

出版信息

Open Med (Wars). 2019 Jan 4;14:32-40. doi: 10.1515/med-2019-0006. eCollection 2019.

Abstract

Folate metabolism makes a crucial contribution towards late-onset Alzheimer's disease (LOAD). Moreover, methylenetetrahydrofolate reductase (MTHFR) constitutes the primary enzyme of the folate pathway. We hypothesize that there is an association of C677T polymorphism in the MTHFR gene with the susceptibility to LOAD. Previous published research has investigated the link between the MTHFR C677T polymorphisms and LOAD susceptibility; nevertheless, the findings have continued to be not only controversial, but also indecisive. Accordingly, we carried out the present meta-analysis for the assessment of the potential link that exists between the MTHFR C677T polymorphism and the susceptibility to LOAD. Furthermore, we carried out a literature search of the PubMed, EMBASE, Cochrane Library, and WanFang database up to August 10, 2018. The odds ratios (ORs) with the respective 95% confidence interval (95%CI) were put to use for the evaluation of the robustness of the link of the MTHFR C677T polymorphism with the vulnerability to LOAD. All statistical analyses were carried out using STATA 15.0. An aggregate of 14 case-control research works was retrieved, involving 2,467 LOAD patients as well as 2,877 controls. We found that a substantial link exists between C677T polymorphism and LOAD risk in a codominant framework (TC vs. CC: OR=1.22, 95%CI=1.00-1.49, P=0.049). In addition to the stratified analysis based on ethnicity, which suggested that C677T polymorphism was likely linked only to an augmented threat of LOAD in Asians, it did not exist among Caucasians. Furthermore, in the subgroup analysis carried out using APOE ɛ4 status, a substantial increase in the susceptibility to LOAD was detected in APOE ɛ4 carriers as well as non-APOE ɛ4 carriers. In sum, the current meta-analysis revealed that MTHFR C677T polymorphism was associated with susceptibility to LOAD. Further extensive case-control studies are required.

摘要

叶酸代谢对晚发型阿尔茨海默病(LOAD)起着至关重要的作用。此外,亚甲基四氢叶酸还原酶(MTHFR)是叶酸代谢途径的主要酶。我们假设MTHFR基因中的C677T多态性与LOAD易感性之间存在关联。先前发表的研究已经探讨了MTHFR C677T多态性与LOAD易感性之间的联系;然而,研究结果不仅一直存在争议,而且尚无定论。因此,我们进行了本荟萃分析,以评估MTHFR C677T多态性与LOAD易感性之间存在的潜在联系。此外,我们对截至2018年8月10日的PubMed、EMBASE、Cochrane图书馆和万方数据库进行了文献检索。使用优势比(OR)及其各自的95%置信区间(95%CI)来评估MTHFR C677T多态性与LOAD易感性之间联系的稳健性。所有统计分析均使用STATA 15.0进行。共检索到14项病例对照研究,涉及2467例LOAD患者和2877例对照。我们发现,在共显性模型中,C677T多态性与LOAD风险之间存在显著联系(TC与CC相比:OR = 1.22,95%CI = 1.00 - 1.49,P = 0.049)。除了基于种族的分层分析表明C677T多态性可能仅与亚洲人LOAD风险增加有关,而在白种人中不存在这种关联外。此外,在使用APOEɛ4状态进行的亚组分析中,在APOEɛ4携带者和非APOEɛ4携带者中均检测到LOAD易感性显著增加。总之,当前的荟萃分析表明MTHFR C677T多态性与LOAD易感性有关。需要进一步进行广泛的病例对照研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ee/6325648/c4e24bcd49c5/med-14-032-g001.jpg

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