Low physical activity accentuates the effect of the FTO rs9939609 polymorphism on body fat accumulation
- Camilla H. Andreasen, MSc (cila{at}novonordisk.com)1,
- Kirstine L. Stender-Petersen, MSc1,
- Mette S. Mogensen, BSc1,
- Signe S. Torekov, MSc1,
- Lise Wegner, MSc1,
- Gitte Andersen, PhD1,
- Arne L. Nielsen, MSc1,
- Anders Albrechtsen, MSc2,
- Knut Borch-Johnsen, DMSc1,,3,,4,
- Signe S. Rasmussen, MD1,
- Jesper O. Clausen, DMSc1,
- Annelli Sandbæk, PhD5,
- Torsten Lauritzen, DMSc5,
- Lars Hansen, DMSc6,
- Torben Jørgensen, DMSc3,
- Oluf Pedersen, DMSc1,,4 and
- Torben Hansen, PhD1
- 1Steno Diabetes Center, Gentofte, Denmark;
- 2Department of biostatistics, University of Copenhagen, Denmark;
- 3Research Centre for Prevention and Health, Glostrup University Hospital, Glostrup, Denmark;
- 4Faculty of Health Science, University of Aarhus, Aarhus, Denmark;
- 5Department of General Practice, University of Aarhus, Aarhus, Denmark.
- 6 Science and Medicine, Novo Nordisk A/S, Bagsværd, Denmark
Abstract
Objective: Recently three independent studies have shown that variation in the fat mass and obesity associated gene (FTO) associates with BMI and obesity. In the present study, the effect of FTO variation on metabolic traits including obesity, type 2 diabetes and related quantitative phenotypes was examined.
Research Design and Methods: The FTO rs9939609 polymorphism was genotyped in a total of 17,508 Danes, comprising five different study groups.
Results: In studies of 3,856 type 2 diabetic cases and 4,861 normal glucose tolerant control subjects the minor A-allele of rs9939609 associated with type 2 diabetes (p=9·10-5, OR 1.13 [1.06-1.20]). This association was abolished when adjusting for BMI (p=0.2, OR 1.06 [0.97-1.16]). Among 17,162 middle-aged Danes, the A-allele associated with overweight (p=1·10-12, OR 1.19 [1.13-1.24]) and obesity (p=2·10-16, OR 1.27 [1.20-1.34]). Furthermore, obesity-related quantitative traits such as body weight, waist circumference, fat mass, and fasting serum leptin levels were significantly elevated in A-allele carriers. An interaction between the FTO rs9939609 genotype and physical activity (p=0.007) was found, where physically inactive homozygous risk A-allele carriers had an increase in BMI level by 1.95±0.3 kg/m2 compared with homozygous T-allele carriers.
Conclusions: We validate that variation in FTO is associated with type 2 diabetes when not adjusted for BMI and with an overall increase in body fat mass. Furthermore, low physical activity seems to accentuate the effect of FTO rs9939609 on body fat accumulation.
Footnotes
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- Received July 4, 2007.
- Accepted October 10, 2007.
- Copyright © American Diabetes Association











