Literature DB >> 2044638

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

M J Tikkanen1, J P Ojala, E Helve.   

Abstract

Subanalyses of previous multicenter studies comparing lovastatin and gemfibrozil were carried out to evaluate the merits of these agents in patients with different serum lipid phenotypes (type 2a and 2b hyperlipoproteinemia). Regardless of phenotype, lovastatin was more effective in lowering LDL-cholesterol, while gemfibrozil had a greater triglyceride-lowering and HDL-cholesterol-increasing effect. Patients with type 2a phenotype benefited (in terms of serum lipid pattern) more from lovastatin. In type 2b hyperlipoproteinemia, more patients taking lovastatin than gemfibrozil reached both treatment goals defined by the European Atherosclerosis Society, (LDL-cholesterol 4.0 mmol/l and triglycerides 2.3 mmol/l). In many patients these goals could not be met suggesting that multiple drug therapy may be indicated in part of the patients with type 2b hyperlipoproteinemia.

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Year:  1991        PMID: 2044638

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  11 in total

1.  Treatment of combined hyperlipidemia with lovastatin versus gemfibrozil: a comparison study.

Authors:  J P Ojala; E Helve; M J Tikkanen
Journal:  Cardiology       Date:  1990       Impact factor: 1.869

Review 2.  Plasma lipid transfer proteins.

Authors:  A R Tall
Journal:  J Lipid Res       Date:  1986-04       Impact factor: 5.922

3.  Comparison of lovastatin and probucol in treatment of familial and non-familial hypercholesterolemia: different effects on lipoprotein profiles.

Authors:  E Helve; M J Tikkanen
Journal:  Atherosclerosis       Date:  1988-08       Impact factor: 5.162

Review 4.  Fibric acids: effects on lipids and lipoprotein metabolism.

Authors:  S M Grundy; G L Vega
Journal:  Am J Med       Date:  1987-11-27       Impact factor: 4.965

5.  Helsinki Heart Study: primary-prevention trial with gemfibrozil in middle-aged men with dyslipidemia. Safety of treatment, changes in risk factors, and incidence of coronary heart disease.

Authors:  M H Frick; O Elo; K Haapa; O P Heinonen; P Heinsalmi; P Helo; J K Huttunen; P Kaitaniemi; P Koskinen; V Manninen
Journal:  N Engl J Med       Date:  1987-11-12       Impact factor: 91.245

6.  Comparison between lovastatin and gemfibrozil in the treatment of primary hypercholesterolemia: the Finnish Multicenter Study.

Authors:  M J Tikkanen; E Helve; A Jäättelä; E Kaarsalo; A Lehtonen; W Malbecq; H Oksa; P Pääkkönen; J Salmi; T Veharanta
Journal:  Am J Cardiol       Date:  1988-11-11       Impact factor: 2.778

7.  Gemfibrozil: effect on serum lipids, lipoproteins, postheparin plasma lipase activities and glucose tolerance in primary hypertriglyceridaemia.

Authors:  E A Nikkilä; R Ylikahri; J K Huttunen
Journal:  Proc R Soc Med       Date:  1976

8.  Suppression of apolipoprotein B production during treatment of cholesteryl ester storage disease with lovastatin. Implications for regulation of apolipoprotein B synthesis.

Authors:  H N Ginsberg; N A Le; M P Short; R Ramakrishnan; R J Desnick
Journal:  J Clin Invest       Date:  1987-12       Impact factor: 14.808

9.  The recognition and management of hyperlipidaemia in adults: A policy statement of the European Atherosclerosis Society.

Authors: 
Journal:  Eur Heart J       Date:  1988-05       Impact factor: 29.983

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

Authors:  P Schulzeck; M Bojanovski; A Jochim; H Canzler; D Bojanovski
Journal:  Lancet       Date:  1988-03-19       Impact factor: 79.321

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  1 in total

1.  Lipoprotein composition and oxidative modification during therapy with gemfibrozil and lovastatin in patients with combined hyperlipidaemia.

Authors:  M Vázquez; D Zambón; Y Hernández; T Adzet; M Merlos; E Ros; J C Laguna
Journal:  Br J Clin Pharmacol       Date:  1998-03       Impact factor: 4.335

  1 in total

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