Share this article on:

The metabolic effects of lopinavir/ritonavir in HIV-negative men

Lee, Grace Aa,b; Seneviratne, Taraa,b; Noor, Mustafa Aa,b; Lo, Joan Cb,c; Schwarz, Jean-Marcb,c,d; Aweeka, Francesca Te; Mulligan, Kathleenb,c; Schambelan, Morrisb,c; Grunfeld, Carla,b

Clinical Science

Background: Therapy with HIV protease inhibitors (PI) has been shown to worsen glucose and lipid metabolism, but whether these changes are caused by direct drug effects, changes in disease status, or body composition is unclear. Therefore, we tested the effects of the PI combination lopinavir and ritonavir on glucose and lipid metabolism in HIV-negative subjects.

Methods: A dose of 400 mg lopinavir/100 mg ritonavir was given twice a day to 10 HIV-negative men. Fasting glucose and insulin, lipid and lipoprotein profiles, oral glucose tolerance, insulin sensitivity by euglycemic hyperinsulinemic clamp, and body composition were determined before and after lopinavir/ritonavir treatment for 4 weeks.

Results: On lopinavir/ritonavir, there was an increase in fasting triglyceride (0.89 ± 0.15 versus 1.63 ± 0.36 mmol/l; P = 0.007), free fatty acid (FFA; 0.33 ± 0.04 versus 0.43 ± 0.06 mmol/l; P = 0.001), and VLDL cholesterol (15.1 ± 2.6 versus 20 ± 3.3 mg/dl; P = 0.05) levels. There were no changes in fasting LDL, HDL, IDL, lipoprotein (a), or total cholesterol levels. Fasting glucose, insulin, and insulin-mediated glucose disposal were unchanged, but on a 2 h oral glucose tolerance test glucose and insulin increased. There were no changes in weight, body fat, or abdominal adipose tissue by computed tomography.

Conclusion: Treatment with 4 weeks of lopinavir/ritonavir in HIV-negative men causes an increase in triglyceride levels, VLDL cholesterol, and FFA levels. Lopinavir/ritonavir leads to a deterioration in glucose tolerance at 2 h, but there is no significant change in insulin-mediated glucose disposal rate by euglycemic hyperinsulinemic clamp.

From the a Metabolism and Endocrine Sections, San Francisco Department of Veterans Affairs Medical Center, San Francisco, CA, USA; bDepartment of Medicine, University of California, San Francisco, CA, USA; cDivision of Endocrinology, San Francisco General Hospital, San Francisco, CA, USA; dDepartment of Nutritional Sciences, University of California, Berkeley, CA, USA; eDepartment of Pharmacology University of California, San Francisco, CA,USA.

Correspondence to Grace A. Lee, Department of Veterans Affairs Medical Center, Metabolism Section (111F), San Francisco, CA 94121, USA.

E-mail: galee@itsa.ucsf.edu

Received: 29 May 2003; revised: 2 July; accepted: 15 July 2003.

© 2004 Lippincott Williams & Wilkins, Inc.