The protease inhibitor combination lopinavir/ritonavir does not decrease insulin secretion in healthy, HIV-seronegative volunteers

AIDS. 2010 Jan 16;24(2):265-70. doi: 10.1097/QAD.0b013e328333af1c.

Abstract

Background: HIV protease inhibitors have been shown to worsen glucose and lipid metabolism. Recent studies have suggested that protease inhibitors can impair insulin secretion in HIV-infected patients. We studied the effects of the protease inhibitor combination lopinavir and ritonavir on insulin secretion, insulin sensitivity, and lipid metabolism in HIV-negative persons.

Methods: A combination dose of lopinavir 400 mg and ritonavir 100 mg was given twice daily to eight HIV-seronegative men for 4 weeks. Fasting glucose, insulin, lipid, and lipoprotein profiles; oral glucose tolerance; insulin secretion and insulin-mediated glucose disposal by hyperglycemic clamp; and body composition by dual energy X-ray absorptiometry were determined before and after lopinavir/ritonavir administration.

Results: There was no change in first-phase insulin secretion (2.82 +/- 0.30 versus 2.71 +/- 0.31 nmol/l; P = 0.60), as well as fasting insulin and glucose levels, oral glucose tolerance, or insulin-mediated glucose disposal after 4 weeks administration of lopinavir/ritonavir. However, there were significant increases in fasting triglycerides (1.02 +/- 0.13 versus 2.20 +/- 0.31 mmol/l; P = 0.001), total cholesterol (4.42 +/- 0.30 versus 5.70 +/- 0.60 mmol/l; P = 0.007), and apo B-100 levels (0.86 +/- 0.07 versus 1.07 +/- 0.11 g/l; P = 0.0009). High-density lipoprotein cholesterol decreased (0.99 +/- 0.11 versus 0.82 +/- 0.10 mmol/l; P = 0.005). There were no changes in body composition, weight, or body fat.

Conclusion: Although administration of lopinavir/ritonavir to healthy, HIV-seronegative volunteers for 4 weeks resulted in increased triglyceride and decreased high-density lipoprotein cholesterol levels, there was no change in first-phase insulin secretion during the hyperglycemic clamp. The reported effects of protease inhibitor on insulin secretion in HIV-infected individuals may be due to changes in HIV-related factors and not a direct drug effect.

Trial registration: ClinicalTrials.gov NCT00525239.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Blood Glucose / metabolism
  • Cholesterol / metabolism
  • Drug Combinations
  • Glucose Clamp Technique
  • HIV Protease Inhibitors / administration & dosage
  • HIV Protease Inhibitors / pharmacology*
  • HIV Seronegativity*
  • Humans
  • Insulin / metabolism*
  • Insulin Secretion
  • Lipid Metabolism / drug effects
  • Lipoproteins / metabolism
  • Lopinavir
  • Male
  • Middle Aged
  • Pyrimidinones / administration & dosage
  • Pyrimidinones / pharmacology*
  • Ritonavir / administration & dosage
  • Ritonavir / pharmacology*
  • Triglycerides / metabolism

Substances

  • Blood Glucose
  • Drug Combinations
  • HIV Protease Inhibitors
  • Insulin
  • Lipoproteins
  • Pyrimidinones
  • Triglycerides
  • lipoprotein cholesterol
  • Lopinavir
  • Cholesterol
  • Ritonavir

Associated data

  • ClinicalTrials.gov/NCT00525239