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Diabetes DOI:10.2337/db16-1565

A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in Associated With Reduced Energy Expenditure in American Indians.

Publication TypeJournal Article
Year of Publication2017
AuthorsPiaggi, P, Masindova, I, Muller, YL, Mercader, J, Wiessner, GB, Chen, P, Kobes, S, Hsueh, W-C, Mongalo, M, Knowler, WC, Krakoff, J, Hanson, RL, Bogardus, C, Baier, LJ
Corporate AuthorsConsortium, SIGMATD2
JournalDiabetes
Volume66
Issue8
Pages2284-2295
Date Published2017 08
ISSN1939-327X
KeywordsAdiposity, Adult, Alleles, Arizona, Basal Metabolism, Body Mass Index, Calorimetry, Diabetes Mellitus, Type 2, Energy Metabolism, Female, Genetic Variation, Genome-Wide Association Study, Humans, Indians, North American, Male, Middle Aged, Receptors, G-Protein-Coupled
Abstract

Pima Indians living in Arizona have a high prevalence of obesity, and we have previously shown that a relatively lower energy expenditure (EE) predicts weight and fat mass gain in this population. EE is a familial trait (heritability = 0.52); therefore, in the current study, we aimed to identify genetic variants that affect EE and thereby influence BMI and body fatness in Pima Indians. Genotypic data from 491,265 variants were analyzed for association with resting metabolic rate (RMR) and 24-h EE assessed in a whole-room calorimeter in 507 and 419 Pima Indians, respectively. Variants associated with both measures of EE were analyzed for association with maximum BMI and percent body fat (PFAT) in 5,870 and 912 Pima Indians, respectively. rs11014566 nominally associated with both measures of EE and both measures of adiposity in Pima Indians, where the G allele (frequency: Pima Indians = 0.60, Europeans <0.01) associated with lower 24-h EE (β = -33 kcal/day per copy), lower RMR (β = -31 kcal/day), higher BMI (β = +0.6 kg/m), and higher PFAT (β = +0.9%). However, the association of rs11014566 with BMI did not directionally replicate when assessed in other ethnic groups. rs11014566 tags rs144895904, which affected promoter function in an in vitro luciferase assay. These variants map to , which is highly expressed in the brain and interacts with two other genes ( and ) known to affect obesity in knockout mice. Our results suggest that common ethnic-specific variation in may influence EE; however, its role in weight gain remains controversial, as it either had no association with BMI or associated with BMI but in the opposite direction in other ethnic groups.

DOI10.2337/db16-1565
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/28476931?dopt=Abstract

Alternate JournalDiabetes
PubMed ID28476931
PubMed Central IDPMC5521859