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A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

Lookup NU author(s): Professor Mark Walker

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Abstract

Obesity is a serious international health problem that increases the risk of several common diseases. The genetic factors predisposing to obesity are poorly understood. A genome-wide search for type 2 diabetes-susceptibility genes identified a common variant in the FTO (fat mass and obesity associated) gene that predisposes to diabetes through an effect on body mass index (SMI). An additive association of the variant with Ml was replicated in 13 cohorts with 38,759 participants. The 16% of adults who are homozygous for the risk allele weighed about 3 kilograms more and had 1.67-fold increased odds of obesity when compared with those not inheriting a risk allele. This association was observed from age 7 years upward and reflects a specific increase in fat mass.


Publication metadata

Author(s): Frayling TM, Timpson NJ, Weedon MN, Zeggini E, Freathy RM, Lindgren CM, Perry JRB, Elliott KS, Lango H, Rayner NW, Shields B, Harries LW, Barrett JC, Ellard S, Groves CJ, Knight B, Patch A-M, Ness AR, Ebrahim S, Lawlor DA, Ring SM, Ben-Shlomo Y, Jarvelin M-R, Sovio U, Bennett AJ, Melzer D, Ferrucci L, Loos RJF, Barroso I, Wareham NJ, Karpe F, Owen KR, Cardon LR, Walker M, Hitman GA, Palmer CNA, Doney ASF, Morris AD, Smith GD, Hattersley AT, McCarthy MI

Publication type: Article

Publication status: Published

Journal: Science

Year: 2007

Volume: 316

Issue: 5826

Pages: 889-894

ISSN (print): 0036-8075

ISSN (electronic): 1095-9203

Publisher: American Association for the Advancement of Science

URL: http://dx.doi.org/10.1126/science.1141634

DOI: 10.1126/science.1141634

PubMed id: 17434869


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Funding

Funder referenceFunder name
Wellcome Trust
079557Wellcome Trust
090532Wellcome Trust
G0500070Medical Research Council
G0000934Medical Research Council
G0600705Medical Research Council
G9815508Medical Research Council
MC_U106179471Medical Research Council
MC_U106188470Medical Research Council
Z99 AG999999Intramural NIH HHS

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