American Journal of Kidney Diseases
Volume 39, Issue 1 , Pages 67-75, January 2002

Fluvastatin improves lipid abnormalities in patients with moderate to advanced chronic renal insufficiency☆☆

Department of Nephrology, Sahlgrenska University Hospital, Göteborg, Sweden; and the Lipid and Lipoprotein Laboratory, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Received 2 May 2001; received in revised form 20 July 2001; accepted 20 July 2001.

Abstract 

Chronic renal insufficiency is characterized by specific abnormalities in lipoprotein metabolism, affecting both apolipoprotein A (apo A)- and apo B-containing lipoproteins. To evaluate the effects of fluvastatin, a synthetic 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, on renal dyslipoproteinemia, we performed a randomized, double-blind, placebo-controlled, two-way, period cross-over study. Study patients were administered fluvastatin, 40 mg/d, or placebo during 8 weeks in randomized order. Forty-five nonnephrotic patients (28 men, 17 women) without diabetes with moderate to advanced chronic renal insufficiency participated in the study. Their mean age was 56.4 ± 11.0 years. Glomerular filtration rate ranged from 12 to 44 mL/min/1.73 m2 of body surface area (mean, 27.5 ± 10.5 mL/min/1.73 m2). Fluvastatin treatment resulted in significant reductions in the primary outcome variables low-density lipoprotein cholesterol (LDL-C; −26%; P < 0.001), apo B (−21%; P < 0.001), and lipoprotein B complex (Lp-Bc) (−14%; P < 0.01). There were statistically significant differences between fluvastatin and placebo treatment for the secondary outcome variables total cholesterol (−19%), triglycerides (TGs; −13%), VLDL-C (−13%), apo E (−13%), and Lp-B (−22%). There was no treatment effect on high-density lipoprotein cholesterol or lipoprotein(a). Fluvastatin treatment was well tolerated, with no serious adverse events during the study. In conclusion, fluvastatin treatment was well tolerated in patients with moderately advanced renal insufficiency and led to a significant reduction in cholesterol-rich, but to a lesser extent in TG-rich, apo B-containing lipoproteins. It remains to be clarified whether these positive changes in lipoprotein profile also will result in attenuation of the atherosclerotic process in these patients, as well as beneficially affect the progression of chronic renal failure. © 2002 by the National Kidney Foundation, Inc.

Keywords:  Chronic renal insufficiency, lipids, lipoproteins (Lp), apolipoproteins (apo), fluvastatin

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 Supported in part by a research grant from AstraZeneca, Mölndal, Sweden.

☆☆ Address reprint requests to Ola Samuelsson, MD, PhD, Department of Nephrology, Sahlgrenska University Hospital, S-413 45 Göteborg, Sweden. E-mail: ola.samuelsson@medic.gu.se

 0272-6386/02/3901-0010$35.00/0

PII: S0272-6386(02)72374-3

American Journal of Kidney Diseases
Volume 39, Issue 1 , Pages 67-75, January 2002