Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/17138
Title: Common variants near MC4R are associated with fat mass, weight and risk of obesity.
Authors: Loos, RJ
Lindgren, CM
Li, S
Wheeler, E
Zhao, JH
Prokopenko, I
Inouye, M
Freathy, RM
Attwood, AP
Beckmann, JS
Berndt, SI
Prostate
Lung
Colorectal
and Ovarian (PLCO) Cancer Screening Trial
Jacobs, KB
Chanock, SJ
Hayes, RB
Bergmann, S
Bennett, AJ
Bingham, SA
Bochud, M
Brown, M
Cauchi, S
Connell, JM
Cooper, C
Smith, GD
Day, I
Dina, C
De, S
Dermitzakis, ET
Doney, AS
Elliott, KS
Elliott, P
Evans, DM
Sadaf Farooqi I
Froguel, P
Ghori, J
Groves, CJ
Gwilliam, R
Hadley, D
Hall, AS
Hattersley, AT
Hebebrand, J
Heid, IM
KORA
Lamina, C
Gieger, C
Illig, T
Meitinger, T
Wichmann, HE
Herrera, B
Hinney, A
Hunt, SE
Jarvelin, MR
Johnson, T
Jolley, JD
Karpe, F
Keniry, A
Khaw, KT
Luben, RN
Mangino, M
Marchini, J
McArdle, WL
McGinnis, R
Meyre, D
Munroe, PB
Morris, AD
Ness, AR
Neville, MJ
Nica, AC
Ong, KK
O'Rahilly, S
Owen, KR
Palmer, CN
Papadakis, K
Potter, S
Pouta, A
Qi, L
Nurses' Health Study
Randall, JC
Rayner, NW
Ring, SM
Sandhu, MS
Scherag, A
Sims, MA
Song, K
Soranzo, N
Speliotes, EK
Diabetes Genetics Initiative
Syddall, HE
Teichmann, SA
Timpson, NJ
Tobias, JH
Uda, M
SardiNIA, Study
Vogel, CI
Wallace, C
Waterworth, DM
Weedon, MN
Wellcome Trust Case Control Consortium
Willer, CJ
FUSION
Wraight
Yuan, X
Zeggini, E
Hirschhorn, JN
Strachan, DP
Ouwehand, WH
Caulfield, MJ
Samani, NJ
Frayling, TM
Vollenweider, P
Waeber, G
Mooser, V
Deloukas, P
McCarthy, MI
Wareham, NJ
Barroso, I
Jacobs, KB
Chanock, SJ
Hayes, RB
Lamina, C
Gieger, C
Illig, T
Meitinger, T
Wichmann, HE
Kraft, P
Hankinson, SE
Hunter, DJ
Hu, FB
Lyon, HN
Voight, BF
Ridderstrale, M
Groop, L
Scheet, P
Sanna, S
Abecasis, GR
Albai, G
Nagaraja, R
Schlessinger, D
Jackson, AU
Tuomilehto, J
Collins, FS
Boehnke, M
Mohlke, KL
First Published: Jun-2008
Citation: NAT GENET, 2008, 40 (6), pp. 768-775
Abstract: To identify common variants influencing body mass index (BMI), we analyzed genome-wide association data from 16,876 individuals of European descent. After previously reported variants in FTO, the strongest association signal (rs17782313, P = 2.9 x 10(-6)) mapped 188 kb downstream of MC4R (melanocortin-4 receptor), mutations of which are the leading cause of monogenic severe childhood-onset obesity. We confirmed the BMI association in 60,352 adults (per-allele effect = 0.05 Z-score units; P = 2.8 x 10(-15)) and 5,988 children aged 7-11 (0.13 Z-score units; P = 1.5 x 10(-8)). In case-control analyses (n = 10,583), the odds for severe childhood obesity reached 1.30 (P = 8.0 x 10(-11)). Furthermore, we observed overtransmission of the risk allele to obese offspring in 660 families (P (pedigree disequilibrium test average; PDT-avg) = 2.4 x 10(-4)). The SNP location and patterns of phenotypic associations are consistent with effects mediated through altered MC4R function. Our findings establish that common variants near MC4R influence fat mass, weight and obesity risk at the population level and reinforce the need for large-scale data integration to identify variants influencing continuous biomedical traits.
DOI Link: 10.1038/ng.140
eISSN: 1546-1718
Links: http://hdl.handle.net/2381/17138
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

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