Literature DB >> 2894548

Comparison between simvastatin and bezafibrate in effect on plasma lipoproteins and apolipoproteins in primary hypercholesterolaemia.

P Schulzeck1, M Bojanovski, A Jochim, H Canzler, D Bojanovski.   

Abstract

The ability of simvastatin, a competitive inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, to lower lipid levels in 16 patients with primary hypercholesterolaemia was compared with that of bezafibrate in a 16-week, double-blind, parallel, placebo-controlled trial that was continued in an open crossover fashion. Simvastatin was better than bezafibrate at lowering total and low-density lipoprotein (LDL)-cholesterol and apolipoprotein B concentrations (30.4% [p less than 0.001], 37.3% [p less than 0.001], and 37.8% [p less than 0.001] vs 17.0%, 19.6%, and 24.0%, respectively). Both drugs increased the high-density lipoprotein (HDL)-cholesterol and apolipoprotein A-I, but this change was significant only with bezafibrate (p less than 0.05). Bezafibrate and simvastatin reduced triglycerides by 25.6% (p less than 0.001) and 13.7% (p less than 0.05), respectively. Very low-density lipoprotein (VLDL)-cholesterol was significantly reduced only by bezafibrate (44.3%, p less than 0.001). Both drugs were tolerated well and no serious side-effects were noted. The results show that simvastatin was more effective than bezafibrate in lowering total-cholesterol, LDL-cholesterol, and apolipoprotein B, while bezafibrate was better at lowering triglycerides and VLDL-cholesterol and at raising HDL-cholesterol and apolipoprotein A-I.

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Year:  1988        PMID: 2894548     DOI: 10.1016/s0140-6736(88)91414-6

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  9 in total

1.  [Lipid status and basal steroid hormone level following 16 weeks of lovastatin therapy in primary hypercholesterolemia].

Authors:  W Stürmer; E P Kromer; A J Riegger; K Kochsiek
Journal:  Klin Wochenschr       Date:  1991-05-03

Review 2.  Value of non-drug treatment and drug treatment in hypertension.

Authors:  L J Beilin
Journal:  Drugs       Date:  1988       Impact factor: 9.546

Review 3.  Simvastatin. A review of its pharmacological properties and therapeutic potential in hypercholesterolaemia.

Authors:  P A Todd; K L Goa
Journal:  Drugs       Date:  1990-10       Impact factor: 9.546

4.  Effects of simvastatin and fenofibrate on serum lipoproteins and apolipoproteins in primary hypercholesterolaemia.

Authors:  R Stohler; U Keller; W F Riesen
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

5.  Lovastatin and gemfibrozil in the treatment of type 2a and type 2b hyperlipoproteinemia.

Authors:  M J Tikkanen; J P Ojala; E Helve
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

Review 6.  Bezafibrate. An update of its pharmacology and use in the management of dyslipidaemia.

Authors:  K L Goa; L B Barradell; G L Plosker
Journal:  Drugs       Date:  1996-11       Impact factor: 9.546

7.  Simvastatin and bezafibrate: effects on serum lipoproteins and lecithin: cholesterol acyltransferase activity in familial hypercholesterolaemia.

Authors:  P Weisweiler
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

8.  Clinical experience with simvastatin compared with cholestyramine.

Authors:  D W Erkelens; M G Baggen; J J Van Doormaal; M Kettner; J C Koningsberger; M J Mol
Journal:  Drugs       Date:  1988       Impact factor: 9.546

9.  Effect of simvastatin on high density lipoprotein subfractions and apolipoproteins in type IIa hypercholesterolemia.

Authors:  D Crook; R Bruce; M Worthington; D Mulcahy; D Patterson; V Wynn
Journal:  Cardiovasc Drugs Ther       Date:  1992-12       Impact factor: 3.727

  9 in total

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