Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network study

Pharmacogenet Genomics. 2009 Feb;19(2):161-9. doi: 10.1097/FPC.0b013e32831e030e.

Abstract

Background: The apolipoproteins (APOA1/C3/A4/A5) are key components in modulating lipoprotein metabolism. It is unknown whether variants at the APOA1/C3/A4/A5 gene cluster are associated with lipid response to pharmacologic intervention.

Methods and results: Plasma triglycerides (TGs) and high-density lipoprotein (HDL) levels were measured in 861 Genetics of Lipid-Lowering Drugs and Diet Network study participants who underwent a 3-week fenofibrate trial. We examined 18 common single nucleotide polymorphisms (SNPs) spanning the APOA1/C3/A4/A5 genes to investigate the effects of variants at the gene cluster on lipid response to fenofibrate treatment. We found that the minor alleles of the SNPs rs3135506 (APOA5_S19W), rs5104 (APOA4_N147S), rs4520 (APOC3_G34G), and rs5128 (APOC3_3U386) were associated with enhanced TG response to fenofibrate treatment (P= 0.0004-0.018). The minor allele of SNP rs2854117 (APOC3_M482) was associated with reduced rather than enhanced TG response (P= 0.026). The SNP rs3135506 (APOA5_S19W) was associated with HDL response, with minor allele related to reduced HDL response to fenofibrate (P= 0.002). Association analyses on haplotype provided corroborative evidence to single SNP association analyses. The common haplotypes H2, H3, and H5 were significantly associated with reduced TG response to fenofibrate.

Conclusion: The genetic variants at APOA1/C3/A4/A5 gene cluster may be useful markers to predict response of lipid-lowering therapy with fenofibrate. Further studies to replicate/confirm our findings are warranted.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Apolipoprotein A-I / genetics
  • Apolipoprotein A-V
  • Apolipoprotein C-III / genetics
  • Apolipoproteins / genetics*
  • Apolipoproteins A / genetics
  • Diet
  • Female
  • Fenofibrate / therapeutic use*
  • Genetic Variation
  • Genotype
  • Haplotypes
  • Humans
  • Hypertriglyceridemia / drug therapy*
  • Hypertriglyceridemia / genetics*
  • Hypolipidemic Agents / therapeutic use*
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • Multigene Family / genetics*
  • Pharmacogenetics
  • Polymorphism, Single Nucleotide

Substances

  • APOA1 protein, human
  • APOA5 protein, human
  • Apolipoprotein A-I
  • Apolipoprotein A-V
  • Apolipoprotein C-III
  • Apolipoproteins
  • Apolipoproteins A
  • Hypolipidemic Agents
  • apolipoprotein A-IV
  • Fenofibrate