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携带 MTHFR 基因 C677T 多态性的 T 变体等位基因时,妊娠糖尿病的患病率增加:系统评价和荟萃分析。

Increasing prevalence of gestational diabetes mellitus when carrying the T variant allele of the MTHFR gene C677T polymorphism: a systematic review and meta-analysis.

机构信息

Center for Systems Biology, Department of Bioinformatics, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, 215123, China.

Medical College, Soochow University, Suzhou, 215123, China.

出版信息

Arch Gynecol Obstet. 2022 May;305(5):1193-1202. doi: 10.1007/s00404-021-06303-4. Epub 2021 Oct 25.

DOI:10.1007/s00404-021-06303-4
PMID:34694432
Abstract

PURPOSE

Previous epidemiological data linking the C677T and A1298C MTHFR polymorphisms to gestational diabetes risk have been mixed and controversial. Therefore, we conducted this meta-analysis to derive a more precise estimation of the relationship between MTHFR polymorphisms and this pregnancy disorder.

METHODS

A systematic literature search for original epidemiological studies was performed in the CNKI, WanFang, Cochrane Library, PubMed, and Web of Science databases. R language-based programs were employed for all statistical analyses. Odds ratios and corresponding 95% confidence intervals were calculated to estimate the effects of the variant allele on gestational diabetes risk.

RESULTS

A summary of the estimates for the C677T polymorphism showed that the exposure cohorts were prone to gestational diabetes by a greater magnitude than the control groups. Further subgroup analysis by ethnicity showed that the Asians carrying the variant T allele were more susceptible to this pregnancy disorder. However, the pathogenic effect was not evident in the non-Asian subgroup. For the A1298C polymorphism, no statistical significance could be detected.

CONCLUSION

This meta-analysis suggests that the T allele of the MTHFR gene C677T polymorphism tends to increase gestational diabetes susceptibility, especially for Asians. However, the A1298C polymorphism is not associated with an increased risk of this crippling pregnancy disorder.

摘要

目的

先前将 MTHFR 基因 C677T 和 A1298C 多态性与妊娠糖尿病风险联系起来的流行病学数据存在差异且存在争议。因此,我们进行了这项荟萃分析,以更准确地评估 MTHFR 多态性与这种妊娠疾病之间的关系。

方法

在中国知网、万方、 Cochrane 图书馆、PubMed 和 Web of Science 数据库中进行了原始流行病学研究的系统文献检索。使用基于 R 语言的程序进行所有统计分析。计算比值比和相应的 95%置信区间,以估计变异等位基因对妊娠糖尿病风险的影响。

结果

对 C677T 多态性的估计值的总结表明,暴露组比对照组更容易发生妊娠糖尿病。按种族进一步亚组分析表明,携带变异 T 等位基因的亚洲人更容易患上这种妊娠疾病。然而,在非亚洲亚组中,这种致病作用并不明显。对于 A1298C 多态性,未检测到统计学意义。

结论

这项荟萃分析表明,MTHFR 基因 C677T 多态性的 T 等位基因倾向于增加妊娠糖尿病的易感性,特别是对亚洲人而言。然而,A1298C 多态性与这种致残妊娠疾病的风险增加无关。

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