1. The Association Between the Peroxisome Proliferator-Activated Receptor-γ2 (PPARG2) Pro12Ala Gene Variant and Type 2 Diabetes Mellitus: A HuGE Review and Meta-Analysis
- Author
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Manjinder S. Sandhu, Julian P T Higgins, Gurdeep S. Sagoo, Anne-Helen Harding, Jan Yates, and Hebe N. Gouda
- Subjects
Peroxisome proliferator-activated receptor gamma ,Epidemiology ,Population ,review ,030209 endocrinology & metabolism ,Genome-wide association study ,Type 2 diabetes ,Bioinformatics ,Genetic Heterogeneity ,03 medical and health sciences ,0302 clinical medicine ,Gene Frequency ,Genetic model ,medicine ,Humans ,genetics ,Genetic Predisposition to Disease ,education ,030304 developmental biology ,2. Zero hunger ,0303 health sciences ,education.field_of_study ,Polymorphism, Genetic ,business.industry ,Genetic heterogeneity ,Type 2 Diabetes Mellitus ,Odds ratio ,medicine.disease ,3. Good health ,meta-analysis ,PPAR gamma ,Diabetes Mellitus, Type 2 ,HUMAN GENOME EPIDEMIOLOGY (HuGE) REVIEW ,Regression Analysis ,genome, human ,business - 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.
- Published
- 2010