Associations between SLCO1B1, APOE and CYP2C9 and lipid-lowering efficacy and pharmacokinetics of fluvastatin: a meta-analysis

Pharmacogenomics. 2023 Jun;24(8):475-484. doi: 10.2217/pgs-2023-0004. Epub 2023 Jun 15.

Abstract

Objective: This meta-analysis was designed to investigate the associations between SLCO1B1, APOE and CYP2C9 and the lipid-lowering effects and pharmacokinetics of fluvastatin. Methods: Studies were searched from inception to March 2023, including three SNPs related to fluvastatin, SLCO1B1, CYP2C9 and APOE. Weighted mean differences and corresponding 95% CIs were analyzed to evaluate the associations between SNPs and outcomes. Results: SLCO1B1 521T>C was associated with lower total cholesterol and low-density lipoprotein reduction. Patients carrying 521CC or total cholesterol had a significantly higher area under the curve than those carrying 521TT, but no significant difference existed. Conclusion: CYP2C9 and SLCO1B1 may be associated with the efficacy and pharmacokinetics of fluvastatin.

Keywords: fluvastatin; hyperlipidemia; pharmacogenetics; pharmacokinetics; polymorphism.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoproteins E
  • Cholesterol*
  • Cytochrome P-450 CYP2C9 / genetics
  • Fluvastatin
  • Genotype
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors* / pharmacokinetics
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors* / therapeutic use
  • Liver-Specific Organic Anion Transporter 1 / genetics

Substances

  • Fluvastatin
  • Cytochrome P-450 CYP2C9
  • Cholesterol
  • Apolipoproteins E
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • CYP2C9 protein, human
  • SLCO1B1 protein, human
  • Liver-Specific Organic Anion Transporter 1