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Effect of pravastatin on body composition and markers of cardiovascular disease in HIV-infected men - A randomized, placebo-controlled study

  • Patrick W.G. Mallon
  • , John Miller
  • , Jason C. Kovacic
  • , Julia Kent-Hughes
  • , Richard Norris
  • , Katherine Samaras
  • , Michael P. Feneley
  • , David A. Cooper
  • , Andrew Carr

Research output: Contribution to journalArticlepeer-review

86 Scopus citations

Abstract

Objectives: To determine the effect of the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, pravastatin, on markers of cardiovascular risk and lipodystrophy in HIV-infected, protease inhibitor (PI)-treated men with hypercholesterolaemia. Methods: A randomized, placebo-controlled, 16-week study was carried out on 33 HIV-infected, hypercholesterolaemic men (fasting total cholesterol > 6.5mmol/L) on PI-containing therapy. Patients commenced dietary assessment and advice at week 0 and were randomized to 12 weeks pravastatin (40 mg each night) or placebo from week 4. The primary endpoint was the time-weighted change (TWAUC) in total cholesterol from week 0. Secondary endpoints included TWAUC cholesterol from week 4 (start of pravastatin), total and regional body fat, fasting lipids, glucose, insulin, and markers of cardiovascular risk. Results: Of 33 men randomized (pravastatin n = 16, mean age 48 years), 31 completed the study. Groups were matched for baseline cholesterol and body composition. Although there was no significant between-group difference in TWAUC cholesterol from week 0 (pravastatin -0.6 ± 1.0 versus placebo -0.4 ± 1.0 mmol/L/week; P= 0.8), TWAUC cholesterol from week 4 decreased more in the pravastatin group (-0.8 ± 1.0 versus -0.3 ± 0.9 mmol/L/week; P = 0.04). Neither triglycerides nor dietary intake changed. Subcutaneous fat increased significantly with pravastatin (+0.72 ± 1.55 versus +0.19 ± 0.48 kg change in limb fat, P < 0.04; +5.2 ± 8.7 versus -1.3 ± 13.7 cm2 change in abdominal subcutaneous fat, P = 0.02). Apart from homocystine, which decreased in the pravastatin group, there were no significant differences in other cardiovascular, lipid or glucose parameters. Conclusions: Despite limited effects on cholesterol, 12 weeks use of pravastatin 40 mg each night in HIV-infected men with hypercholesterolaemia resulted in significant increases in subcutaneous fat.

Original languageEnglish
Pages (from-to)1003-1010
Number of pages8
JournalAIDS
Volume20
Issue number7
DOIs
StatePublished - Apr 2006
Externally publishedYes

Keywords

  • Antiretroviral
  • Cardiovascular risk
  • HIV
  • HMG Co-A reductase inhibitor
  • Hyperlipidaemia
  • Lipodystrophy
  • Pravastatin
  • Statin
  • Toxicity

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