Combined effects of MC4R and FTO common genetic variants on obesity in European general populations
- 3 March 2009
- journal article
- research article
- Published by Springer Nature in Journal of Molecular Medicine
- Vol. 87 (5), 537-546
- https://doi.org/10.1007/s00109-009-0451-6
Abstract
Genome-wide association scans recently identified common polymorphisms, in intron 1 of FTO and 188 kb downstream MC4R, that modulate body mass index (BMI) and associate with increased risk of obesity. Although their individual contribution to obesity phenotype is modest, their combined effects and their interactions with environmental factors remained to be evaluated in large general populations from birth to adulthood. In the present study, we analyzed independent and combined effects of the FTO rs1421085 and MC4R rs17782313 risk alleles on BMI, fat mass, prevalence and incidence of obesity and subsequent type 2 diabetes (T2D) as well as their interactions with physical activity levels and gender in two European prospective population-based cohorts of 4,762 Finnish adolescents (NFBC 1986) and 3,167 French adults (D.E.S.I.R.). Compared to participants carrying neither FTO nor MC4R risk allele (20–24% of the populations), subjects with three or four risk alleles (7–10% of the populations) had a 3-fold increased susceptibility of developing obesity during childhood. In adults, their combined effects were more modest (~1.8-fold increased risk) and associated with a 1.27% increase in fat mass (P = 0.001). Prospectively, we demonstrated that each FTO and MC4R risk allele increased obesity and T2D incidences by 24% (P = 0.02) and 21% (P = 0.02), respectively. However, the effect on T2D disappeared after adjustment for BMI. The Z-BMI and ponderal index of newborns homozygous for the rs1421085 C allele were 0.1 units (P = 0.02) and 0.27 g/cm3 (P = 0.005) higher, respectively, than in those without FTO risk allele. The MC4R rs17782313 C allele was more associated with obesity and fat mass deposition in males than in females (P = 0.003 and P = 0.03, respectively) and low physical activity accentuated the effect of the FTO polymorphism on BMI increase and obesity prevalence (P = 0.008 and P = 0.01, respectively). In European general populations, the combined effects of common polymorphisms in FTO and MC4R are therefore additive, predictive of obesity and T2D, and may be influenced by interactions with physical activity levels and gender, respectively.This publication has 30 references indexed in Scilit:
- Physical Activity and the Association of Common FTO Gene Variants With Body Mass Index and ObesityArchives of Internal Medicine, 2008
- FTO Gene Associated Fatness in Relation to Body Fat Distribution and Metabolic Traits throughout a Broad Range of FatnessPLOS ONE, 2008
- Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTOvariants confer a significant riskBMC Medical Genetics, 2008
- Major gender difference in association of FTO gene variant among severely obese children with obesity and obesity related phenotypesBiochemical and Biophysical Research Communications, 2008
- Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related TraitsPLoS Genetics, 2007
- Variation in FTO contributes to childhood obesity and severe adult obesityNature Genetics, 2007
- Large quantitative effect of melanocortin-4 receptor gene mutations on body mass indexJournal of Medical Genetics, 2004
- Proposed criteria for the diagnosis of diabetes: evidence from a French epidemiological study (D.E.S.I.R.).1997
- Targeted Disruption of the Melanocortin-4 Receptor Results in Obesity in MiceCell, 1997
- Attributable risk percent in case-control studies.Journal of Epidemiology and Community Health, 1971