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Genet Mol Res ; 12(3): 3324-34, 2013 Sep 03.
Article in English | MEDLINE | ID: mdl-24065674

ABSTRACT

Uncoupling protein 2 (UCP2) is a mitochondrial transporter protein and can affect the function of ß-cells. We investigated a possible association between functional UCP2 -866G/A and Ala55Val polymorphisms and type 2 diabetes in 715 Hubei Han Chinese. No significant association was found, either for the -866G/A polymorphism (allele, P = 0.254; genotype, P = 0.508) or for the Ala55Val polymorphism (allele, P = 0.250; genotype, P = 0.896). Then, we reviewed the association of UCP2 -866G/A and Ala55Val polymorphisms with type 2 diabetes susceptibility in the Chinese population with a meta-analysis. Our meta-analysis, which included 3643 Chinese, further confirmed a lack of association of -866G/A and Ala55Val with type 2 diabetes (additive model: -866G/A, odds ratio = 1.09, 95% confidence interval = 0.94-1.27, P = 0.25; Ala55Val, odds ratio = 1.21, 95% confidence interval = 0.85-1.72, P = 0.28). Based on our case-control study and meta-analysis, we conclude that UCP2 Ala55Val and -866G/A polymorphisms are not significantly associated with type 2 diabetes risk in the Chinese population.


Subject(s)
Diabetes Mellitus, Type 2/genetics , Genetic Association Studies , Ion Channels/genetics , Mitochondrial Proteins/genetics , Obesity/genetics , Case-Control Studies , China , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/pathology , Genetic Predisposition to Disease , Genetics, Population , Humans , Obesity/complications , Obesity/pathology , Polymorphism, Single Nucleotide , Promoter Regions, Genetic , Risk Factors , Uncoupling Protein 2 , White People
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