A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants inGPR158Associated With Reduced Energy Expenditure in American Indians
Author(s) -
Paolo Piaggi,
Ivica Mašindová,
Yunhua L. Muller,
Josep M. Mercader,
Gregory Wiessner,
Peng Chen,
Sayuko Kobes,
WenChi Hsueh,
Milliejoan Mongalo,
William C. Knowler,
Jonathan Krakoff,
Robert L. Hanson,
Clifton Bogardus,
Leslie J. Baier
Publication year - 2017
Publication title -
diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.219
H-Index - 330
eISSN - 1939-327X
pISSN - 0012-1797
DOI - 10.2337/db16-1565
Subject(s) - genotyping , genome wide association study , association (psychology) , energy expenditure , genetics , genetic association , biology , computational biology , evolutionary biology , genotype , single nucleotide polymorphism , psychology , gene , endocrinology , psychotherapist
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/m2), 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 GPR158, which is highly expressed in the brain and interacts with two other genes (RGS7 and CACNA1B) known to affect obesity in knockout mice. Our results suggest that common ethnic-specific variation in GPR158 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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom