Lovastatin in the Treatment of Multifactorial Hyperlipidemia Associated With Proteinuria

Thomas A. Golper, D. Roger Illingworth, Cynthia D. Morris, William M. Bennett

Research output: Contribution to journalArticlepeer-review

61 Scopus citations


The efficacy and safety of lovastatin as a hypolipidemic agent were evaluated in ten adult patients with secondary hypocchoeesterolemia due to proteinuria (>2 g/d) and (in seven patients) concurrent corticosteroid therapy. Patients were on a low-cholesterol diet throughout the study. After a 4-week baseline period, patients were randomized to receive either placebo or 10 mg lovastatin twice daily for a period of 6 weeks. The dose of lovastatin was increased to 20 mg twice daily for 6 weeks, and 40 mg twice daily for 6 weeks in the latter group. Those patients who received placebo for the first 6 weeks subsequently received 10, 20, and 40 mg of lovastatin twice daily in a stepped dose regimen, with each dose given for 6 weeks. Lovastatin was well tolerated by all patients and none withdrew from the study. Baseline plasma cholesterol concentrations (390 ± 20 mg/dL; mean ± SEM) decreased 22% (P < 0.003) at the lowest dose of 10 mg twice daily, 27% at 20 mg twice daily, and 33% at 40 mg twice daily. Baseline plasma triglycerides decreased by 25% (P < 0.05) at the highest dosage. Concentrations of low-density lipoprotein (LDL) cholesterol fell by 29%, 34%, and 45% on doses of 10, 20, and 40 mg of lovastatin twice daily. Concentrations of high-density lipoprotein (HDL) cholesterol increased slightly. Serum creatinine concentrations and proteinuria were not affected by lovastatin therapy. We conclude that lovastatin was a well-tolerated and extremely effective hypocholesterolemic agent in patients with persistent secondary hype rcholesterolemia associated with proteinuria or proteinuria and concurrent corticosteroid therapy.

Original languageEnglish (US)
Pages (from-to)312-320
Number of pages9
JournalAmerican Journal of Kidney Diseases
Issue number4
StatePublished - 1989


  • Proteinuria
  • hyperlipidemia
  • lovastatin
  • plasma cholesterol

ASJC Scopus subject areas

  • Nephrology


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