PLoS Genetics (Jan 2010)

Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels.

  • Wilmar Igl,
  • Asa Johansson,
  • James F Wilson,
  • Sarah H Wild,
  • Ozren Polasek,
  • Caroline Hayward,
  • Veronique Vitart,
  • Nicholas Hastie,
  • Pavao Rudan,
  • Carsten Gnewuch,
  • Gerd Schmitz,
  • Thomas Meitinger,
  • Peter P Pramstaller,
  • Andrew A Hicks,
  • Ben A Oostra,
  • Cornelia M van Duijn,
  • Igor Rudan,
  • Alan Wright,
  • Harry Campbell,
  • Ulf Gyllensten,
  • EUROSPAN Consortium

DOI
https://doi.org/10.1371/journal.pgen.1000798
Journal volume & issue
Vol. 6, no. 1
p. e1000798

Abstract

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Genome-wide association studies (GWAS) have identified 38 larger genetic regions affecting classical blood lipid levels without adjusting for important environmental influences. We modeled diet and physical activity in a GWAS in order to identify novel loci affecting total cholesterol, LDL cholesterol, HDL cholesterol, and triglyceride levels. The Swedish (SE) EUROSPAN cohort (N(SE) = 656) was screened for candidate genes and the non-Swedish (NS) EUROSPAN cohorts (N(NS) = 3,282) were used for replication. In total, 3 SNPs were associated in the Swedish sample and were replicated in the non-Swedish cohorts. While SNP rs1532624 was a replication of the previously published association between CETP and HDL cholesterol, the other two were novel findings. For the latter SNPs, the p-value for association was substantially improved by inclusion of environmental covariates: SNP rs5400 (p(SE,unadjusted) = 3.6 x 10(-5), p(SE,adjusted) = 2.2 x 10(-6), p(NS,unadjusted) = 0.047) in the SLC2A2 (Glucose transporter type 2) and rs2000999 (p(SE,unadjusted) = 1.1 x 10(-3), p(SE,adjusted) = 3.8 x 10(-4), p(NS,unadjusted) = 0.035) in the HP gene (Haptoglobin-related protein precursor). Both showed evidence of association with total cholesterol. These results demonstrate that inclusion of important environmental factors in the analysis model can reveal new genetic susceptibility loci.