Browse by author
Lookup NU author(s): Michelle Baker, Nicole Gaukrodger, Dr Helen Imrie, Hannah Watkins, Dr Peter Avery, Professor Bernard Keavney
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Rare mutations in the proopiomelanocortin (POMC) gene cause severe early-onset childhood obesity. However, it is unknown whether common variants in POMC are responsible for variation in body weight or fat distribution within the commonly observed range in the population. We tested for association between three polymorphisms spanning the POMC gene and obesity phenotypes in 1,428 members of 248 families. There was significant association between genotypes at the C8246T (P < 0.0001) and C1032G (P = 0.003) polymorphisms and waist-to-hip ratio (WHR) corrected for age, sex, smoking, exercise, and alcohol consumption. Each T allele at C8246T (or G allele at C1032G) was associated with a 0.2-SD–higher WHR in a codominant fashion. When WHR was additionally corrected for BMI, thus providing a measure of body fat distribution throughout the range of BMI, there remained significant evidence for association with both markers that was of similar magnitude and statistical significance. There was no association between genotype at any polymorphism and BMI or plasma leptin level. These data show that genetic variants at the POMC locus influence body fat distribution within the normal range, suggesting a novel role for POMC in metabolic regulation.
Author(s): Baker M, Gaukrodger N, Mayosi B, Imrie H, Farrall ML, Watkins H, Connell JMC, Avery PJ, Keavney BD
Publication type: Article
Publication status: Published
Journal: Diabetes
Year: 2005
Volume: 54
Issue: 8
Pages: 2492-2496
ISSN (print): 0012-1797
ISSN (electronic): 1939-327X
Publisher: American Diabetes Association
URL: http://dx.doi.org/10.2337/diabetes.54.8.2492
DOI: 10.2337/diabetes.54.8.2492
Altmetrics provided by Altmetric