Boosting dose ritonavir does not alter peripheral insulin sensitivity in healthy HIV-seronegative volunteers

J Acquir Immune Defic Syndr. 2010 Nov;55(3):361-4. doi: 10.1097/QAI.0b013e3181e6a7d9.

Abstract

Background: Some HIV protease inhibitors (PIs), including full-dose ritonavir (800 mg) and ritonavir-boosted lopinavir, acutely induce insulin resistance in the absence of HIV infection and changes in body composition. Boosting dose ritonavir (100-200 mg) is the most commonly prescribed PI, yet its effects on glucose metabolism have not been described in the absence of another PI.

Methods: In this randomized, double-blind, cross-over study, a single dose of ritonavir 200 mg or placebo was given to healthy HIV-seronegative volunteers before assessment of insulin sensitivity by euglycemic hyperinsulinemic clamp.

Results: Boosting dose ritonavir had no effect on insulin-mediated glucose disposal (M/I, placebo: 8.59 ± 0.83 vs. ritonavir: 8.51 ± 0.64 mg/kg per minute per μU/mL insulin, P = 0.89).

Conclusions: A single boosting dose of ritonavir does not alter insulin sensitivity, suggesting lopinavir is likely responsible for the induction of insulin resistance demonstrated in prior short-term studies of lopinavir/ritonavir. There is a dose-dependent effect of ritonavir on insulin sensitivity.

Trial registration: ClinicalTrials.gov NCT00525239.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Aged
  • Anti-HIV Agents / administration & dosage
  • Anti-HIV Agents / adverse effects*
  • Cross-Over Studies
  • Double-Blind Method
  • Female
  • Glucose / metabolism
  • Human Experimentation
  • Humans
  • Insulin / physiology*
  • Insulin Resistance*
  • Male
  • Middle Aged
  • Placebos / administration & dosage
  • Ritonavir / administration & dosage
  • Ritonavir / adverse effects*

Substances

  • Anti-HIV Agents
  • Insulin
  • Placebos
  • Glucose
  • Ritonavir

Associated data

  • ClinicalTrials.gov/NCT00525239