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多民族人群中rs1801133基因型患2型糖尿病的风险评估:一项全球荟萃流行病学研究

Determining the Risk of Type 2 Diabetes for rs1801133 Genotypes in Multiethnic Populations: A Global Meta-Epidemiological Study.

作者信息

Nurkolis Fahrul, Amalia Nurlinah, Tandi Yosi Yohanes Putra, Athallah Ariq Fadhil, Aditya Muhammad Reva, Nojaid Ammar, Humardani Farizky Martriano, Prapriatna Achmad Fabiansyah, Taslim Nurpudji Astuti, Harbuwono Dante Saksono, Tjandrawinata Raymond Rubianto

机构信息

Faculty of Medicine, Universitas Airlangga, Surabaya 60132, Indonesia.

Medical Research Center of Indonesia, Surabaya 60281, Indonesia.

出版信息

Int J Mol Sci. 2025 Apr 23;26(9):3987. doi: 10.3390/ijms26093987.

Abstract

The rs1801133 (C677T) polymorphism of the methylenetetrahydrofolate reductase (MTHFR) gene has been linked to type 2 diabetes (T2D) risk. This study aimed to assess the association between rs1801133 genotypes (CC, CT, TT) and T2D across multiethnic populations and to identify genotype- and region-specific risks. A global meta-epidemiological analysis was conducted using data from 19 studies comprising 6479 participants from Asia, Africa, Europe, and America. Odds ratios (OR) and 95% confidence intervals (CIs) were calculated using random-effects models. Subgroup analyses by region were also performed. The results of the CC vs. CT dominant genetic model were OR 95% CI = 0.63 (0.46-0.87); = 0.005; the CC vs. TT genetic recessive model yielded OR 95% CI = 0.59 (0.38-0.91); = 0.02; and the CT vs. TT codominance genetic model yielded OR 95% CI = 0.95 (0.65-1.37); = 0.78. Based on the subgroup analysis, the CC genotype is predominantly associated with an increased risk of T2D in both Africa and Europe. From this study, the CC genotype was proven to be highly contributory to T2D risk compared to the CT and TT genotypes. These findings highlight the need for ethnicity-informed genetic screening and targeted prevention strategies in global diabetes management.

摘要

亚甲基四氢叶酸还原酶(MTHFR)基因的rs1801133(C677T)多态性与2型糖尿病(T2D)风险相关。本研究旨在评估多民族人群中rs1801133基因型(CC、CT、TT)与T2D之间的关联,并确定基因型和区域特异性风险。使用来自19项研究的数据进行了全球荟萃流行病学分析,这些研究包括来自亚洲、非洲、欧洲和美洲的6479名参与者。使用随机效应模型计算比值比(OR)和95%置信区间(CI)。还进行了按区域的亚组分析。CC与CT显性遗传模型的结果为OR 95%CI = 0.63(0.46 - 0.87);P = 0.005;CC与TT遗传隐性模型产生的OR 95%CI = 0.59(0.38 - 0.91);P = 0.02;CT与TT共显性遗传模型产生的OR 95%CI = 0.95(0.65 - 1.37);P = 0.78。基于亚组分析,CC基因型在非洲和欧洲均主要与T2D风险增加相关。从本研究可知,与CT和TT基因型相比,CC基因型被证明对T2D风险有高度贡献。这些发现凸显了在全球糖尿病管理中进行种族知情基因筛查和针对性预防策略的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d2f/12071517/4c32a6e9001b/ijms-26-03987-g001.jpg

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