Copy number variations associated with obesity-related traits in African Americans: a joint analysis between GENOA and HyperGEN

Obesity (Silver Spring). 2012 Dec;20(12):2431-7. doi: 10.1038/oby.2012.162. Epub 2012 Jun 22.

Abstract

Obesity is a highly heritable trait and a growing public health problem. African Americans (AAs) are a genetically diverse, yet understudied population with a high prevalence of obesity (BMI >30 kg/m(2)). Recent studies based upon single-nucleotide polymorphisms (SNPs) have identified genetic markers associated with obesity. However, a large proportion of the heritability of obesity remains unexplained. Copy number variation (CNV) has been cited as a possible source of missing heritability in common diseases such as obesity. We conducted a CNV genome-wide association study of BMI in two African-American cohorts from Genetic Epidemiology Network of Arteriopathy (GENOA) and Hypertension Genetic Epidemiology Network (HyperGEN). We performed independent and identical association analyses in each study, then combined the results in a meta-analysis. We identified three CNVs associated with BMI, obesity, and other obesity-related traits after adjusting for multiple testing. These CNVs overlap the PARK2, GYPA, and SGCZ genes. Our results suggest that CNV may play a role in the etiology of obesity in AAs.

Publication types

  • Meta-Analysis
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Black or African American / genetics*
  • Body Mass Index
  • DNA Copy Number Variations*
  • Female
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Glycophorins / genetics*
  • Humans
  • Male
  • Middle Aged
  • Obesity / epidemiology
  • Obesity / genetics*
  • Phenotype
  • Polymorphism, Single Nucleotide*
  • Sarcoglycans / genetics
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • GYPA protein, human
  • Glycophorins
  • Sarcoglycans
  • Ubiquitin-Protein Ligases
  • parkin protein