Steady-state pharmacokinetic interactions of darunavir/ritonavir with lipid-lowering agent rosuvastatin

J Clin Pharmacol. 2012 Jun;52(6):922-31. doi: 10.1177/0091270011407494. Epub 2011 Jun 28.

Abstract

HIV-1 protease inhibitors often cause dyslipidemia, necessitating the use of lipid-lowering agents such as rosuvastatin. However, when given concomitantly, these therapeutic agents often exhibit adverse drug interactions. In this study (phase I open-label trial, n = 12 HIV-1 seronegative participants), the authors assessed the drug interactions between darunavir/ritonavir given in combination with rosuvastatin. Participants were randomized to receive rosuvastatin (10 mg/day) or darunavir/ritonavir (600/100 mg twice daily) alone for 7 days in a crossover design followed by combination therapy for 7 days with intervening 7-day washout periods. Intensive blood sampling for pharmacokinetics and fasting lipids was performed on days 7, 21, and 35. The geometric mean AUC(0-24 h) of rosuvastatin increased from 109 to 161 ng·h/mL (P < .005) and C(max) increased 6.7 to 16.3 ng/mL (P < .001) when coadministered with darunavir/ritonavir. In the presence of darunavir/ritonavir and rosuvastatin, total cholesterol and triglyceride levels increased by 10% (P = .007) and 56% (P = .011), whereas the high-density lipoprotein cholesterol levels decreased by 13% (P = .006) relative to rosuvastatin administration alone. There were no significant adverse events attributable to the coadministration of these drugs. Rosuvastatin levels increase in the presence of darunavir/ritonavir coadministration, whereas the lipid-lowering benefits are blunted. The clinical significance of these changes requires further investigation.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cholesterol / blood
  • Cholesterol, HDL / blood
  • Cross-Over Studies
  • Darunavir
  • Drug Combinations
  • Drug Interactions
  • Female
  • Fluorobenzenes / adverse effects
  • Fluorobenzenes / blood
  • Fluorobenzenes / pharmacokinetics*
  • Fluorobenzenes / pharmacology
  • HIV Protease Inhibitors / adverse effects
  • HIV Protease Inhibitors / blood
  • HIV Protease Inhibitors / pharmacokinetics
  • HIV Protease Inhibitors / pharmacology*
  • Half-Life
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / adverse effects
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / blood
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacokinetics*
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Male
  • Metabolic Clearance Rate / drug effects
  • Middle Aged
  • Pyrimidines / adverse effects
  • Pyrimidines / blood
  • Pyrimidines / pharmacokinetics*
  • Pyrimidines / pharmacology
  • Ritonavir / adverse effects
  • Ritonavir / blood
  • Ritonavir / pharmacokinetics
  • Ritonavir / pharmacology*
  • Rosuvastatin Calcium
  • Sulfonamides / adverse effects
  • Sulfonamides / blood
  • Sulfonamides / pharmacokinetics*
  • Sulfonamides / pharmacology*
  • Time Factors
  • Triglycerides / blood
  • Young Adult

Substances

  • Cholesterol, HDL
  • Drug Combinations
  • Fluorobenzenes
  • HIV Protease Inhibitors
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Pyrimidines
  • Sulfonamides
  • Triglycerides
  • Rosuvastatin Calcium
  • Cholesterol
  • Ritonavir
  • Darunavir