%0 Journal Article
%T Genome wide association study identifies KCNMA1 contributing to human obesity
%A Hong Jiao
%A Peter Arner
%A Johan Hoffstedt
%A David Brodin
%A Beatrice Dubern
%A S¨¦bastien Czernichow
%A Ferdinand van't Hooft
%A Tomas Axelsson
%A Oluf Pedersen
%A Torben Hansen
%A Thorkild IA S£¿rensen
%A Johannes Hebebrand
%A Juha Kere
%A Karin Dahlman-Wright
%A Anders Hamsten
%A Karine Clement
%A Ingrid Dahlman
%J BMC Medical Genomics
%D 2011
%I BioMed Central
%R 10.1186/1755-8794-4-51
%X We performed a GWA analysis in 164 morbidly obese subjects (BMI:body mass index > 40 kg/m2) and 163 Swedish subjects (> 45 years) who had always been lean. The 700 SNPs displaying the strongest association with obesity in the GWA were analyzed in a second cohort comprising 460 morbidly obese subjects and 247 consistently lean Swedish adults. 23 SNPs remained significantly associated with obesity (nominal P< 0.05) and were in a step-wise manner followed up in five additional cohorts from Sweden, France, and Germany together comprising 4214 obese and 5417 lean or population-based control individuals. Three samples, n = 4133, were used to investigate the population-based associations with BMI. Gene expression in abdominal subcutaneous adipose tissue in relation to obesity was investigated for14 adults.Potassium channel, calcium activated, large conductance, subfamily M, alpha member (KCNMA1) rs2116830*G and BDNF rs988712*G were associated with obesity in five of six investigated case-control cohorts. In meta-analysis of 4838 obese and 5827 control subjects we obtained genome-wide significant allelic association with obesity for KCNMA1 rs2116830*G with P = 2.82 ¡Á 10-10 and an odds ratio (OR) based on cases vs controls of 1.26 [95% C.I. 1.12-1.41] and for BDNF rs988712*G with P = 5.2 ¡Á 10-17and an OR of 1.36 [95% C.I. 1.20-1.55]. KCNMA1 rs2116830*G was not associated with BMI in the population-based samples. Adipose tissue (P = 0.0001) and fat cell (P = 0.04) expression of KCNMA1 was increased in obesity.We have identified KCNMA1 as a new susceptibility locus for obesity, and confirmed the association of the BDNF locus at the genome-wide significant level.Several susceptibility loci for high BMI and obesity have recently been identified by genome-wide association (GWA) analyses of both large population-based samples and samples including extreme obese phenotypes [1-11]. Analysis of the latter group is based on the assumption that subjects with an extreme phenotype, such
%U http://www.biomedcentral.com/1755-8794/4/51