Contribution of Type 2 Diabetes Susceptible Gene GCKR Polymorphisms Rs780094 and Rs1260326 to Gestational Diabetes Mellitus: A Meta-Analysis.

Yuke Zhang, Kuangyi Wang, Chenxi Ji, Yansi Lin, Zitong Liu, Jing Chen, Feifei Zheng, Xiaoqin Yang, Yi Sun
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Abstract

Background: There is still no conclusive understanding of whether the glucokinase regulator (GCKR) gene rs780094 and rs1260326 polymorphisms predispose to gestational diabetes mellitus (GDM).

Objective: This systematic review and meta-analysis aimed to determine the effect of the GCKR polymorphisms on GDM susceptibility.

Methods: Seven literature databases were searched (from inception to February 17, 2024) to locate relevant studies included in further meta-analysis. Odds ratio (OR) and 95% confidence intervals (CI) in the pooled population were estimated to assess the effects of the variant allele on GDM risk.

Results: For the rs780094 polymorphism, 13 datasets with 3443 GDM cases and 5930 nondiabetic controls were included. The pooled estimates in the allele model (OR: 1.19, 95% CI: 1.07~1.32), homozygote model (OR: 1.27, 95% CI: 1.10~1.47), dominant model (OR: 1.16, 95% CI: 1.03~1.31), and recessive model (OR: 1.31, 95% CI: 1.09~1.57) suggested that the C allele carriers were prone to GDM. For the rs1260326 polymorphism, five datasets with 1495 cases and 2678 controls were integrated. The statistically significant effect of the C allele was evident in the allele model (OR: 1.12, 95% CI: 1.01~1.24) and the homozygote model (OR: 1.26, 95% CI: 1.03~1.54).

Conclusion: This meta-analysis suggested that the C allele of the rs780094 and rs1260326 polymorphisms in the GCKR gene are significantly associated with increased risk of GDM.

2型糖尿病易感基因GCKR多态性Rs780094和Rs1260326对妊娠期糖尿病的贡献:一项荟萃分析
背景:葡萄糖激酶调节因子(GCKR)基因rs780094和rs1260326多态性是否易患妊娠期糖尿病(GDM)尚无定论。目的:本系统综述和荟萃分析旨在确定GCKR多态性对GDM易感性的影响。方法:检索7个文献数据库(从建库到2024年2月17日),找到相关研究纳入进一步的meta分析。估计合并人群的优势比(OR)和95%置信区间(CI),以评估变异等位基因对GDM风险的影响。结果:rs780094多态性共纳入13个数据集,共3443例GDM病例和5930例非糖尿病对照。等位基因模型(OR: 1.19, 95% CI: 1.07~1.32)、纯合子模型(OR: 1.27, 95% CI: 1.10~1.47)、显性模型(OR: 1.16, 95% CI: 1.03~1.31)和隐性模型(OR: 1.31, 95% CI: 1.09~1.57)的汇总估计表明,C等位基因携带者易患GDM。对于rs1260326多态性,我们整合了1495例病例和2678例对照的5个数据集。在等位基因模型(OR: 1.12, 95% CI: 1.01~1.24)和纯合子模型(OR: 1.26, 95% CI: 1.03~1.54)中,C等位基因的影响具有统计学意义。结论:本荟萃分析提示GCKR基因rs780094和rs1260326多态性的C等位基因与GDM风险增加显著相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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