Inverse effects of the PPARγ2 Pro12Ala polymorphism on measures of adiposity over 15 years in African Americans and whites: The CARDIA study

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Few studies have addressed the association of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor γ2 (PPARγ2) gene with longitudinal measures of adiposity and insulin sensitivity during young adulthood, or reported on its relationship with these outcomes in African Americans. These issues were examined in the biracial Coronary Artery Risk Development in Young Adults (CARDIA) cohort, a population-based sample of 5115 African Americans and whites followed prospectively over 15 years. Frequency of the Ala12 allele was 2.1% in African Americans and 12.8% in whites, consistent with previous reports. A generalized estimating equation method was used to simultaneously examine the cross-sectional and longitudinal relationships between the Pro12Ala polymorphism and the measures of adiposity and insulin sensitivity. The Pro12Ala polymorphism was significantly associated with mean 15-year levels of adiposity, but these associations were in opposite direction in the 2 racial groups. On average, African Americans carrying the Ala12 allele had a 1.1 kg/m2 lower body mass index (BMI) (P =. 02) and whites a 0.6 kg/m2 higher BMI (P =. 01), as compared to Pro12 homozygotes. The Ala12 allele was also significantly associated with a decreased risk of incident insulin resistance syndrome in each race (OR = 0.44, P =. 04 in African Americans; OR = 0.61, P =. 01 in whites) and lower mean 15-year levels of fasting insulin (P =. 02), glucose (P =. 02), and homeostasis model assessment (P =. 01) in African Americans but not in whites. Important roles of BMI and ethnic background in influencing the complex relationships among PPARγ gene variation, adiposity, and insulin resistance are suggested.

Original languageEnglish (US)
Pages (from-to)910-917
Number of pages8
JournalMetabolism: clinical and experimental
Issue number7
StatePublished - Jul 2005

Bibliographical note

Funding Information:
This study is supported by contracts N01-HC-48047, N01-HC-48048, N01-HC-48049, N01-HC-48050, and N01-HC-95095 from the National Heart, Lung, and Blood Institute.

Copyright 2008 Elsevier B.V., All rights reserved.

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