Apolipoprotein-E polymorphism and response to pravastatin in men with coronary artery disease (REGRESS)

Anke-Hilse Maitland-Van Der Zee, J. Wouter Jukema, Aeilko H. Zwinderman, D. Michael Hallman, Anthonius De Boer, John J. R. Kastelein, Peter De Knijff

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Objectve - The influence of ApoE polymorphism on the efficacy of statins in lowering plasma lipids and lipoproteins and improving angiographic parameters was assessed. Methods: ApoE genotypes were studied in a group (n = 815) of well-characterised male coronary artery disease (CAD) patients who participated in the lipid-lowering regression study 'Regression Growth Evaluation Statin Study (REGRESS). Results - There was a significant interaction between treatment (placebo/pravastatin) and APOE genotype when lipid levels were considered, APOE2 + carriers exhibited the largest improvement of HDL levels ( + 0.15 mmol/l) and LDL/HDL ratios (-0.60) compared with APOE3 + ( + 0.06 mmol/l, -0.043, respectively) and APOE4 + carriers ( + 0.07 mmol/l, -0.040). In contrast, APOE2 + allele carriers had the least effect in terms of angiographic parameters, although the difference was not statistically significant. Conclusions - The effects of statins in subjects with different ApoE genotypes were different with regard to the lipoprotein profile, but not with regard to angiographic parameters.
Original languageEnglish
Pages (from-to)327-331
Number of pages5
JournalActa Cardiologica
Volume61
Issue number3
DOIs
Publication statusPublished - Jun 2006

Keywords

  • Apolipoprotein-E polymorphism
  • Coronary artery disease
  • Pharmacogenetics
  • Statin
  • apolipoprotein E
  • high density lipoprotein
  • low density lipoprotein
  • placebo
  • pravastatin
  • allele
  • angiocardiography
  • article
  • clinical trial
  • controlled clinical trial
  • controlled study
  • coronary artery disease
  • drug efficacy
  • drug mechanism
  • genotype
  • human
  • human cell
  • lipid blood level
  • major clinical study
  • male
  • protein polymorphism
  • randomized controlled trial
  • regression analysis

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