Nutrition
Volume 26, Issue 7 , Pages 760-765, July 2010

Melanocortin-3 receptor gene variants: Association with childhood obesity and eating behavior in Chilean families

  • A.M. Obregón, M.Sc.

      Affiliations

    • Department of de Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile
    • Institute of Nutrition and Food Technology (INTA) University of Chile, Santiago, Chile
  • ,
  • P. Amador, M.D.

      Affiliations

    • Department of de Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile
  • ,
  • M. Valladares, B.Sc.

      Affiliations

    • Department of de Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile
    • Institute of Nutrition and Food Technology (INTA) University of Chile, Santiago, Chile
  • ,
  • G. Weisstaub, M.D., M.Sc.

      Affiliations

    • Institute of Nutrition and Food Technology (INTA) University of Chile, Santiago, Chile
  • ,
  • R. Burrows, M.D.

      Affiliations

    • Institute of Nutrition and Food Technology (INTA) University of Chile, Santiago, Chile
  • ,
  • J.L. Santos, Ph.D.

      Affiliations

    • Department of de Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile
    • Corresponding Author InformationCorresponding author. Tel.: +56-23-543-862; fax: +56-26-338-298.

Received 13 March 2009; accepted 1 July 2009. published online 08 February 2010.

Abstract 

Objective

To evaluate the association between melanocortin-3 receptor common genetic polymorphisms with childhood obesity and eating behavior in Chilean families.

Methods

Two hundred twenty-nine obese children (6–12 y old, body mass index >95th percentile of Centers for Disease Control and Prevention/National Center for Health Statistics, 2000) and 270 parents were selected. Genotypes for MC3R genetic markers −239A>G, 17C>A (Thr6Lys), 241G>A (Val81Ile), +2138InsCAGACC, and microsatellite D20s32e were determined. Eating behavior scores were computed using the Child Eating Behavior Questionnaire and a shorter version of the Three Factor Eating Questionnaire adapted for evaluating eating inclinations in children. Genotype-obesity associations were assessed by the Transmission Disequilibrium Test. Non-parametric tests were used to compare eating behavior scores across study groups.

Results

Allelic frequencies of −239G, 17A, 241A, and +2138InsCAGACC were estimated as 4.5%, 5.9%, 5.6%, and 17.6%, respectively, in obese children. The Transmission Disequilibrium Test in case–parent trios revealed no significant associations between childhood obesity and genetic markers, including the microsatellite D20s32e. In girls, we found significantly higher scores of the emotional eating subscale in carriers of the +2138InsCAGACC compared with non-carriers (P=0.04). In boys, carriers of 17A and 241A showed lower scores for the emotional eating subscale (P=0.01), whereas carriers of +2138InsCAGACC showed significantly lower scores for the enjoyment of food subscale compared with non-carriers (P=0.04).

Conclusions

There is not sufficient evidence to support the contribution for common melanocortin-3 receptor variants in childhood obesity. However, our results are concordant for a role of melanocortin-3 receptor variants in some dimensions of eating behavior such as emotional eating and enjoyment of food.

Keywords: Childhood obesity, Eating behavior, Melanocortin receptor, Genetic

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 This study was supported by grant 1061096 from FONDECYT, Chile.

PII: S0899-9007(09)00301-3

doi:10.1016/j.nut.2009.07.005

Nutrition
Volume 26, Issue 7 , Pages 760-765, July 2010