Abstract

BackgroundGenetic factors are important determinants of overweight. We examined whether there are differential effect sizes depending on children's body composition.MethodsWe analysed data of n = 4,837 children recorded in the Avon Longitudinal Study of Parents and Children (ALSPAC), applying quantile regression with sex- and age-specific standard deviation scores (SDS) of body mass index (BMI) or with body fat mass index and fat-free mass index at 9 years as outcome variables and an “obesity-risk-allele score” based on eight genetic variants known to be associated with childhood BMI as the explanatory variable.ResultsThe quantile regression coefficients increased with increasing child's BMI-SDS and fat mass index percentiles, indicating larger effects of the genetic factors at higher percentiles. While the associations with BMI-SDS were of similar size in medium and high BMI quantiles (40th percentile and above), effect sizes with fat mass index increased over the whole fat mass index distribution. For example, the fat mass index of a normal-weight (50th percentile) child was increased by 0.13 kg/m2 (95% confidence interval (CI): 0.09, 0.16) per additional allele, compared to 0.24 kg/m2 per allele (95% CI: 0.15, 0.32) in children at the 90th percentile. The genetic associations with fat-free mass index were weaker and the quantile regression effects less pronounced than those on fat mass index.ConclusionsGenetic risk factors for childhood overweight appear to have greater effects on fatter children. Interaction of known genetic factors with environmental or unknown genetic factors might provide a potential explanation of these findings.

Highlights

  • Increasing prevalence of childhood overweight has been reported worldwide [1]

  • Genetic factors are important determinants of the overweight risk as has been shown in adoption and twin studies [2,3] and in observational studies pointing to the important role of maternal body mass index (BMI) in the development of overweight in children [4,5]

  • Recent genome-wide association (GWA) studies allowed identifying several genetic factors associated with childhood and adult obesity, such as variants of the FTO and MC4R genes [6,7]

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Summary

Methods

We analysed data of n = 4,837 children recorded in the Avon Longitudinal Study of Parents and Children (ALSPAC), applying quantile regression with sex- and age-specific standard deviation scores (SDS) of body mass index (BMI) or with body fat mass index and fat-free mass index at 9 years as outcome variables and an ‘‘obesity-risk-allele score’’ based on eight genetic variants known to be associated with childhood BMI as the explanatory variable

Results
Introduction
Materials and Methods

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