Single variants can explain the association between coronary heart disease and haplotypes in the apolipoprotein(a) locus

Atherosclerosis. 2010 Sep;212(1):193-6. doi: 10.1016/j.atherosclerosis.2010.05.009. Epub 2010 May 13.

Abstract

Objective: LPA encodes apolipoprotein(a), and a CCTC haplotype in the LPA locus is associated with CHD. The 4399Met variant (rs3798220) of LPA has a risk estimate for CHD similar to that of the CCTC haplotype. We asked whether co-incidence with the 4399Met variant explained the association of the haplotype with CHD.

Methods: We stratified by the 4399Met variant and another LPA SNP (rs10455872) associated with CHD and tested the association between CHD and 4 SNPs that define two haplotypes associated with CHD: CCTC and CTTG.

Results: For CCTC, in the presence of the rs3798220 risk allele the OR was 1.68 (95% CI: 1.05-2.68, P=0.03) versus 0.30 (95% CI: 0.06-1.59, P=0.16) with the non-risk allele. For CTTG, in the presence of the rs10455872 risk allele the OR was 1.57 (95% CI: 1.15-2.13, P=0.004) versus 1.04 (95% CI: 0.79-1.35, P=0.77) with the non-risk allele.

Conclusion: The rs3798220 and rs10455872 SNPs explain the association of the CCTC and CTTG haplotypes with CHD.

MeSH terms

  • Apoprotein(a) / genetics*
  • California
  • Case-Control Studies
  • Coronary Disease / genetics*
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Logistic Models
  • Odds Ratio
  • Phenotype
  • Polymorphism, Single Nucleotide*
  • Risk Assessment
  • Risk Factors

Substances

  • Apoprotein(a)