Copy number variations associated with obesity-related traits in African Americans: a joint analysis between GENOA and HyperGEN.
meta_analysis · Level I
Where this comes from
- Record sourced from PubMed, PMID 22836685.
- Also identified by DOI 10.1038/oby.2012.162 and PMC identifier 3484176.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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.
Medical subject headings
- Black or African American
- DNA Copy Number Variations
- Glycophorins
- Obesity
- Polymorphism, Single Nucleotide
- Ubiquitin-Protein Ligases