Analysis of association of gene variants with obesity traits in New Zealand European children at 6 years of age

Mol Biosyst. 2017 Jul 25;13(8):1524-1533. doi: 10.1039/c7mb00104e.

Abstract

Childhood obesity is a public health problem, which is associated with a long-term increased risk of cardiovascular disease and premature mortality. Several gene variants have previously been identified that have provided novel insights into biological factors that contribute to the development of obesity. As obesity tracks through childhood into adulthood, identification of the genetic factors for obesity in early life is important. The objective of this study was to identify putative associations between genetic variants and obesity traits in children at 6 years of age. We recruited 1208 children of mothers from the New Zealand centre of the international Screening for Pregnancy Endpoints (SCOPE) study. Eighty common genetic variants associated with obesity traits were evaluated by the Sequenom assay. Body mass index standardised scores (BMI z-scores) and percentage body fat (PBF; measured by bio-impedance assay (BIA)) were used as anthropometric measures of obesity. A positive correlation was found between BMI z-scores and PBF (p < 0.001, r = 0.756). Two subsets of gene variants were associated with BMI z-scores (HOXB5-rs9299, SH2B1-rs7498665, NPC1-rs1805081 and MSRA-rs545854) and PBF (TMEM18-rs6548238, NPY-rs17149106, ETV-rs7647305, NPY-rs16139, TIMELESS-rs4630333, FTO-rs9939609, UCP2-rs659366, MAP2K5-rs2241423 and FAIM2-rs7138803) in the genotype models. However, there was an absence of overlapping association between any of the gene variants with BMI z-scores and PBF. A further five variants were associated with BMI z-scores (TMEM18-rs6548238, FTO-rs9939609 and MC4R-rs17782313) and PBF (SH2B1-rs7498665 and FTO-rs1421085) once separated by genetic models (additive, recessive and dominant) of inheritance. This study has identified significant associations between numerous gene variants selected on the basis of prior association with obesity and obesity traits in New Zealand European children.

MeSH terms

  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO / genetics*
  • Body Fat Distribution
  • Body Mass Index
  • Child
  • Female
  • Gene Expression
  • Genetic Predisposition to Disease*
  • Genome-Wide Association Study
  • Humans
  • Inheritance Patterns
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Membrane Proteins / genetics*
  • Models, Genetic
  • New Zealand
  • Obesity / diagnosis
  • Obesity / ethnology
  • Obesity / genetics*
  • Obesity / pathology
  • Polymorphism, Single Nucleotide
  • Prospective Studies
  • Receptor, Melanocortin, Type 4 / genetics*
  • White People

Substances

  • Intracellular Signaling Peptides and Proteins
  • MC4R protein, human
  • Membrane Proteins
  • PTTG1IP protein, human
  • Receptor, Melanocortin, Type 4
  • TMEM18 protein, human
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • FTO protein, human