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过氧化物酶体增殖物激活受体-γ2(PPARG2)Pro12Ala 基因变异与 2 型糖尿病的关联:一项 HuGE 综述和荟萃分析。

The association between the peroxisome proliferator-activated receptor-gamma2 (PPARG2) Pro12Ala gene variant and type 2 diabetes mellitus: a HuGE review and meta-analysis.

机构信息

Department of Public Health and Primary Care, University ofCambridge, Cambridge CB2 0SR, UK.

出版信息

Am J Epidemiol. 2010 Mar 15;171(6):645-55. doi: 10.1093/aje/kwp450. Epub 2010 Feb 23.

DOI:10.1093/aje/kwp450
PMID:20179158
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2834889/
Abstract

The peroxisome proliferator-activated receptor-gamma gene (PPARG) has been implicated in the etiology of type 2 diabetes mellitus and has been investigated in numerous epidemiologic studies. In this Human Genome Epidemiology review, the authors assessed this relation in an updated meta-analysis of 60 association studies. Electronic literature searches were conducted on September 14, 2009. Population-based cohort, case-control, cross-sectional, or genome-wide association studies reporting associations between the PPARG Pro12Ala gene variant (rs1801282) and type 2 diabetes were included. An updated literature-based meta-analysis involving 32,849 type 2 diabetes cases and 47,456 controls in relation to the PPARG Pro12Ala variant was conducted. The combined overall odds ratio, calculated by per-allele genetic model random-effects meta-analysis for type 2 diabetes and the Pro12Ala polymorphism, was 0.86 (95% confidence interval: 0.81, 0.90). The analysis indicated a moderate level of heterogeneity attributable to genuine variation in gene effect size (I(2) = 37%). This may reflect the variation observed between ethnic populations and/or differences in body mass index. Work on PPARG Pro12Ala should now focus on the observed heterogeneity in the magnitude of the association between populations. Further investigations into gene-gene and gene-environment interactions may prove enlightening.

摘要

过氧化物酶体增殖物激活受体-γ 基因(PPARG)与 2 型糖尿病的病因学有关,并在许多流行病学研究中进行了研究。在本次人类基因组流行病学综述中,作者通过对 60 项关联研究的更新荟萃分析来评估这种关系。电子文献检索于 2009 年 9 月 14 日进行。纳入了报告 PPARG Pro12Ala 基因变异(rs1801282)与 2 型糖尿病之间关联的基于人群的队列研究、病例对照研究、横断面研究或全基因组关联研究。对与 PPARG Pro12Ala 变异相关的 32849 例 2 型糖尿病病例和 47456 例对照进行了基于文献的更新荟萃分析。通过每等位基因遗传模型随机效应荟萃分析计算出的 2 型糖尿病和 Pro12Ala 多态性的综合总体比值比为 0.86(95%置信区间:0.81,0.90)。分析表明,由于基因效应大小的真实变异引起的异质性处于中等水平(I(2)=37%)。这可能反映了在不同种族人群中观察到的变异,或者反映了体重指数的差异。目前对 PPARG Pro12Ala 的研究应重点关注人群之间关联幅度的观察到的异质性。进一步研究基因-基因和基因-环境相互作用可能会有启发性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a514/2834889/149d8af998eb/amjepidkwp450f01_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a514/2834889/149d8af998eb/amjepidkwp450f01_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a514/2834889/149d8af998eb/amjepidkwp450f01_ht.jpg

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