Novel variants in the putative peroxisome proliferator-activated receptor γ promoter and relationships with obesity in men

3Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Yet unidentified variants within the peroxisome proliferator-activated receptor γ (PPARγ) 2 promoter may explain the inconsistent reports on associations between variants in the coding region and obesity or diabetes. Thus, we examined the putative PPARγ2 promoter (-3371 to +43 bp) for variants in 83 subjects with obesity or type 2 diabetes. We identified eight variants, seven of which were novel, including -792A>G, -816C>T, -882T>C, -1505G>A, -1881C>T, -1884T>A, -2604T>C, and -2953A>G. The variants -816C>T, -1505GA, -1881C>T, and - 2604T>C were in total linkage disequilibrium, and there was a high degree of linkage disequilibrium between several of the novel variants and Pro 12Ala. The novel variants were, together with Pro12Ala and 1431C>T, examined for relationships with obesity among 234 men with early-onset obesity with a BMI at age -20 years of 33.2 ±2.5 kg/m2 and 323 nonobese men with a BMI of 21.7 ±2.5 kg/m2, who were also reexamined after -29 years. The prevalence of the identified variants was not significantly different between the two groups, and the variants did not affect changes in BMI over time. In conclusion, the identified novel variants in the PPARγ2 promoter region do not explain the reported discrepancies in the association of previously identified variants with obesity and type 2 diabetes. Copyright © 2005 NAASO.

Cite

CITATION STYLE

APA

Larsen, T. M., Larsen, L. H., Torekov, S. K., Ek, J., Black, E., Toubro, S., … Pedersen, O. (2005). Novel variants in the putative peroxisome proliferator-activated receptor γ promoter and relationships with obesity in men. Obesity Research, 13(6), 953–958. https://doi.org/10.1038/oby.2005.110

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free