Drug-drug interactions in the treatment of HIV infection: focus on pharmacokinetic enhancement through CYP3A inhibition

J Intern Med. 2010 Dec;268(6):530-9. doi: 10.1111/j.1365-2796.2010.02301.x. Epub 2010 Nov 14.

Abstract

The aim of this review is to discuss the effect of pharmacokinetic drug-drug interactions (DDIs) in the antiretroviral treatment of HIV infection. In particular, but not exclusively, DDIs due to the cytochrome P450 3A (CYP3A) inhibitor ritonavir, which is used to increase antiretroviral drug exposure - a technique known as pharmacokinetic enhancement or 'ritonavir boosting'- will be reviewed. The emphasis here will be on the treatment of important co-morbidities common in patients with HIV, including dyslipidaemia, hypertension, tuberculosis and opiate dependence, as well as on the potentially life-threatening interaction between ritonavir and inhalational steroids, and on the effect of acid-reducing agents on some antiretroviral drugs. Finally, further developments with regard to the use of CYP3A-blocking agents to augment the efficacy of antiviral therapy will be discussed.

Publication types

  • Review

MeSH terms

  • Anti-HIV Agents / pharmacokinetics
  • Anti-HIV Agents / pharmacology*
  • Antitubercular Agents / pharmacology
  • Cytochrome P-450 CYP3A Inhibitors*
  • Drug Interactions
  • Glucocorticoids / pharmacology
  • HIV Infections / drug therapy*
  • HIV Infections / metabolism
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Ritonavir / pharmacology

Substances

  • Anti-HIV Agents
  • Antitubercular Agents
  • Cytochrome P-450 CYP3A Inhibitors
  • Glucocorticoids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Ritonavir