rs12255372 Variant of TCF7L2 Gene Is Protective for Obesity in Mexican Children

Background and Aims Variants in the transcription factor 7-like 2 ( TCF7L2 ) gene are consistently associated with type 2 diabetes in adults, but the association of TCF7L2 with weight-related traits and body fat in humans is unclear. The aim of this study was to determine the relationship between th...

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Veröffentlicht in:Archives of medical research 2011-08, Vol.42 (6), p.495-501
Hauptverfasser: Klünder-Klünder, Miguel, Mejía-Benitez, María Aurora, Flores-Huerta, Samuel, Burguete-García, Ana I, García-Mena, Jaime, Cruz, Miguel
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Sprache:eng
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Zusammenfassung:Background and Aims Variants in the transcription factor 7-like 2 ( TCF7L2 ) gene are consistently associated with type 2 diabetes in adults, but the association of TCF7L2 with weight-related traits and body fat in humans is unclear. The aim of this study was to determine the relationship between the TCF7L2 gene ( rs12255372) and obese phenotype in Mexican school-age children. Methods The study was performed in schools in Mexico City; 186 obese and 194 control children were studied. Fasting insulin and glucose, total cholesterol, LDL-C, HDL-C and triglycerides concentration were determined. The variant rs12255372 of the TCF7L2 gene was genotyped. We used age- and sex-adjusted linear models to test for association with metabolic measurements with this variant. Results Genotype of the TCF7L2 rs12255372 gene was associated with lower fasting plasma glucose ( p  = 0.001) and lower homeostasis model assessment of insulin resistance (HOMA-R; p  = 0.001) in nonobese children. Heterozygous carriers for this variant were more prevalent in lean children (32.5%) than in the obese group (23.7%), which resulted in a strong protective effect for the normal weight condition (OR = 0.56, 0.32–0.97). Conclusions TCF7L2 rs12255372 polymorphism protects Mexican children from obesity. Further research in other large, population-based studies is needed to replicate these findings.
ISSN:0188-4409
1873-5487
DOI:10.1016/j.arcmed.2011.05.006