Multi-variant study of obesity risk genes in African Americans: The Jackson Heart Study

Gene. 2016 Nov 30;593(2):315-21. doi: 10.1016/j.gene.2016.08.041. Epub 2016 Aug 26.

Abstract

Objective: Genome-wide association study (GWAS) has been successful in identifying obesity risk genes by single-variant association analysis. For this study, we designed steps of analysis strategy and aimed to identify multi-variant effects on obesity risk among candidate genes.

Methods: Our analyses were focused on 2137 African American participants with body mass index measured in the Jackson Heart Study and 657 common single nucleotide polymorphisms (SNPs) genotyped at 8 GWAS-identified obesity risk genes.

Results: Single-variant association test showed that no SNPs reached significance after multiple testing adjustment. The following gene-gene interaction analysis, which was focused on SNPs with unadjusted p-value<0.10, identified 6 significant multi-variant associations. Logistic regression showed that SNPs in these associations did not have significant linear interactions; examination of genetic risk score evidenced that 4 multi-variant associations had significant additive effects of risk SNPs; and haplotype association test presented that all multi-variant associations contained one or several combinations of particular alleles or haplotypes, associated with increased obesity risk.

Conclusions: Our study evidenced that obesity risk genes generated multi-variant effects, which can be additive or non-linear interactions, and multi-variant study is an important supplement to existing GWAS for understanding genetic effects of obesity risk genes.

Keywords: Gene-gene interaction; Genetic risk score; Haplotype; Obesity; SNP association.

MeSH terms

  • Adenylyl Cyclases / genetics
  • Black People / genetics*
  • Black or African American
  • Brain-Derived Neurotrophic Factor / genetics
  • Case-Control Studies
  • Cell Adhesion Molecules, Neuronal / genetics
  • Female
  • GPI-Linked Proteins / genetics
  • Haplotypes
  • Humans
  • Male
  • Membrane Proteins / genetics
  • Nerve Tissue Proteins / genetics
  • Obesity / ethnology
  • Obesity / genetics*
  • Polymorphism, Single Nucleotide*
  • Receptor, Melanocortin, Type 4 / genetics
  • Receptors, Gastrointestinal Hormone / genetics
  • Receptors, Nicotinic / genetics
  • Transcription Factor AP-2 / genetics

Substances

  • Brain-Derived Neurotrophic Factor
  • Cell Adhesion Molecules, Neuronal
  • GPI-Linked Proteins
  • MC4R protein, human
  • Membrane Proteins
  • NEGR1 protein, human
  • Nerve Tissue Proteins
  • Receptor, Melanocortin, Type 4
  • Receptors, Gastrointestinal Hormone
  • Receptors, Nicotinic
  • TFAP2B protein, human
  • TMEM18 protein, human
  • Transcription Factor AP-2
  • neurexin IIIalpha
  • nicotinic receptor subunit alpha3
  • BDNF protein, human
  • gastric inhibitory polypeptide receptor
  • Adenylyl Cyclases
  • adenylate cyclase 3