[HTML][HTML] Prospective Analysis of the Association of a Common Variant of FTO (rs9939609) with Adiposity in Children: Results of the IDEFICS Study

F Lauria, A Siani, K Bammann, R Foraita, I Huybrechts… - PLoS one, 2012 - journals.plos.org
F Lauria, A Siani, K Bammann, R Foraita, I Huybrechts, L Iacoviello, AC Koni, Y Kourides…
PLoS one, 2012journals.plos.org
Objectives We investigated cross-sectionally and longitudinally the relationship between
FTO rs9939609 and obesity-related characteristics in the European children of the IDEFICS
project and the interaction of this variant with a lifestyle intervention. Population and
Methods A cohort of 16224 children (2–9 years) was recruited into a population-based
survey (T0) from eight European countries. A second survey (T1) reassessed the children
two years later. A random sample of 4405 children was extracted for genetic studies. 3168 …
Objectives
We investigated cross-sectionally and longitudinally the relationship between FTO rs9939609 and obesity-related characteristics in the European children of the IDEFICS project and the interaction of this variant with a lifestyle intervention.
Population and Methods
A cohort of 16224 children (2–9 years) was recruited into a population-based survey (T0) from eight European countries. A second survey (T1) reassessed the children two years later. A random sample of 4405 children was extracted for genetic studies. 3168 children were re-examined two years later. Half of them underwent a lifestyle intervention program. The FTO rs9939609 was genotyped. Weight, height, waist circumference, triceps and subscapular skinfolds were measured at T0 and T1.
Results
At T0, the risk A allele of rs9939609 was significantly associated with higher values of body mass index (BMI), waist circumference and skinfolds (age, sex, and country-adjusted p-values: all p<0.001) and with a statistically significant increased risk of overweight/obesity.
Over the two year follow-up, no interaction between genotype and intervention was observed. The A allele was associated to a significantly higher increase in all the anthropometric variables examined at T0 independently from the study group (intervention versus control) (p-values: all p<0.002, adjusted for age, sex, country, intervention/control study group, T0 values, and individual time interval between T0 and T1). Over the two-year follow–up, 210 new cases of overweight/obesity occurred. A statistically significant higher incidence of overweight/obesity was associated to the A allele [ORA = 1.95, 95% CI = (1.29; 2.97)].
Conclusions
We confirmed the association between the FTO rs9939609 and body mass and overweight/obesity risk in European children. The main finding of the study is that the A allele carriers present higher increase of body mass and central adiposity over time and higher risk of developing overweight/obesity during growth, independently from intervention measures.
PLOS