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亚甲基四氢叶酸还原酶 1298A>C 多态性与炎症性肠病风险增加相关:来自荟萃分析的证据。

The methylenetetrahydrofolate reductase 1298 A>C polymorphism is associated with an increased risk of inflammatory bowel disease: evidence from a meta-analysis.

机构信息

Department of Anesthesiology, The First Affiliated Hospital of Chengdu Medical College, Chengdu, P.R. China.

Department of Pathology and Pathophysiology, Chengdu Medical College, Chengdu, P.R. China.

出版信息

Expert Rev Clin Immunol. 2021 Nov;17(11):1221-1229. doi: 10.1080/1744666X.2021.1982384. Epub 2021 Sep 28.

DOI:10.1080/1744666X.2021.1982384
PMID:34528870
Abstract

OBJECTIVE

The association between genetic variants in methylenetetrahydrofolate reductase (MTHFR) and risk for inflammatory bowel disease (IBD) has been widely studied. However, the results are equivocal. In this meta-analysis, we aimed to determine the association between MTHFR polymorphisms and susceptibility to IBD.

METHODS

We retrieved studies from the PubMed, Web of Science, Ovid, and China National Knowledge Infrastructure databases. Data were analyzed using STATA software; odds ratios (OR) and confidence intervals (CI) were calculated using fixed or random effects models.

RESULTS

A marginally significant association of the MTHFR 677 C > T polymorphism and patients' IBD risk was observed in the overall analysis (OR = 1.11, 95% CI, 1.01-1.23), but not in the analysis of high-quality studies. However, for the MTHFR 1298 A > C polymorphism, a significant association was found between the MTHFR 1298 AC/CC genotypes and IBD risk in the overall analysis (OR = 1.26, 95% CI, 1.10-1.44), in the high-quality studies (OR = 1.20, 95% CI, 1.02-1.41), and in patients with ulcerative colitis (OR = 1.28, 95% CI, 1.10-1.48).

CONCLUSIONS

Evidence from this meta-analysis indicates that the MTHFR 1298 A > C polymorphism may be responsible for susceptibility to IBD and ulcerative colitis.

摘要

目的

亚甲基四氢叶酸还原酶(MTHFR)基因变异与炎症性肠病(IBD)风险之间的关联已得到广泛研究。然而,结果存在争议。在这项荟萃分析中,我们旨在确定 MTHFR 多态性与 IBD 易感性之间的关联。

方法

我们从 PubMed、Web of Science、Ovid 和中国国家知识基础设施数据库中检索研究。使用 STATA 软件分析数据;使用固定或随机效应模型计算比值比(OR)和置信区间(CI)。

结果

总体分析显示,MTHFR 677C>T 多态性与患者 IBD 风险存在边缘显著关联(OR=1.11,95%CI,1.01-1.23),但在高质量研究的分析中则不然。然而,对于 MTHFR 1298A>C 多态性,总体分析显示 MTHFR 1298AC/CC 基因型与 IBD 风险之间存在显著关联(OR=1.26,95%CI,1.10-1.44),在高质量研究中(OR=1.20,95%CI,1.02-1.41)和溃疡性结肠炎患者中(OR=1.28,95%CI,1.10-1.48)。

结论

这项荟萃分析的证据表明,MTHFR 1298A>C 多态性可能与 IBD 和溃疡性结肠炎的易感性有关。

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