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Candidate gene association study conditioning on individual ancestry in patients with type 2 diabetes and metabolic syndrome from Mexico City
Author(s) -
Cruz M.,
ValladaresSalgado A.,
GarciaMena J.,
Ross K.,
Edwards M.,
AngelesMartinez J.,
OrtegaCamarillo C.,
Escobedo de la Peña J.,
BurgueteGarcia A. I.,
WacherRodarte N.,
Ambriz R.,
Rivera R.,
D'artote A. L.,
Peralta J.,
Parra Esteban J.,
Kumate J.
Publication year - 2010
Publication title -
diabetes/metabolism research and reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.307
H-Index - 110
eISSN - 1520-7560
pISSN - 1520-7552
DOI - 10.1002/dmrr.1082
Subject(s) - tcf7l2 , type 2 diabetes , allele , genetics , biology , candidate gene , snp , body mass index , medicine , genetic association , metabolic syndrome , allele frequency , single nucleotide polymorphism , diabetes mellitus , genotype , endocrinology , gene
Abstract Background Type 2 diabetes (T2D) is influenced by diverse environmental and genetic risk factors. Metabolic syndrome (MS) increases the risk of cardiovascular disease and diabetes. We analysed 14 cases of polymorphisms located in 10 candidate loci, in a sample of patients with T2D and controls from Mexico City. Methods We analysed the association of 14 polymorphisms located within 10 genes ( TCF7L2, ENPP1, ADRB3, KCNJ11, LEPR, PPAR γ, FTO, CDKAL1, SIRT1 and HHEX ) with T2D and MS. The analysis included 519 subjects with T2D defined according to the ADA criteria, 389 with MS defined according to the AHA/NHLBI criteria and 547 controls. Association was tested with the program ADMIXMAP including individual ancestry, age, sex, education and in some cases body mass index (BMI), in a logistic regression model. Results The two markers located within the TCF7L2 gene showed strong associations with T2D (rs7903146, T allele, odd ratio (OR) = 1.76, p = 0.001 and rs12255372, T allele, OR = 1.78, p = 0.002), but did not show significant association with MS. The non‐synonymous rs4994 polymorphism of the ADRB3 gene was associated with T2D (Trp allele, OR = 0.62, p = 0.001) and MS (Trp allele, OR = 0.74, p = 0.018). Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS and the HHEX rs5015480 polymorphism. Conclusions Variants located within the gene TCF7L2 are strongly associated with T2D but not with MS, providing support to previous evidence indicating that polymorphisms at the TCF7L2 gene increase T2D risk. In contrast, the non‐synonymous ADRB3 rs4994 polymorphism is associated with T2D and MS. Copyright © 2010 John Wiley & Sons, Ltd.