Literature DB >> 2060543

Comparative studies on the influence of different fibrates on serum lipoproteins in endogenous hyperlipoproteinaemia.

L Kłosiewicz-Latoszek1, W B Szostak.   

Abstract

Two trials have been performed in the same patients with hyperlipoproteinaemia Types IIb (12 cases), III (6 cases) and IV (11 cases). In the first study the lipid-lowering properties of bezafibrate, fenofibrate, gemfibrozil, etofibrate and etofylline clofibrate were compared and in a separate trial the influence of combined treatment with gemfibrozil plus colestipol and bezafibrate plus probucol on lipoproteins were investigated. The mean percentage lipid-lowering effect of each fibrate on serum and VLDL fraction was significant in the Types IIb, III and IV patients, but there were significant differences between the fibrates. In general, gemfibrozil and bezafibrate decreased plasma lipid levels more than etofibrate and etofylline clofibrate in Type IIb patients. In Type IV cases gemfibrozil and bezafibrate were significantly potent in reducing the triglyceride level than fenofibrate, etofibrate or etofylline clofibrate. All the fibrates produced an increase in HDL cholesterol, but there were significant differences between them were in the Type IV patients. The influence of fibrates on the LDL fraction was much more variable. In hyperlipoproteinaemia Type IIb, a decrease in both LDL cholesterol and LDL apolipoprotein B was observed. In Type III and IV patients, however, an increase in LDL concentration occurred. The addition of colestipol to gemfibrozil therapy led to a further decrease in total cholesterol, LDL cholesterol and LDL apolipoprotein B in Type IIb patients. In patients with hyperlipoproteinaemia Types III and IV colestipol prevented the increase in LDL concentration after treatment with gemfibrozil alone. The effect of probucol on LDL cholesterol was comparable to that of colestipol. Combined treatment with gemfibrozil and colestipol caused an increase in HDL cholesterol concentration in contrast to combined treatment with bezafibrate and probucol.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 2060543     DOI: 10.1007/bf00315136

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


  33 in total

1.  Gel isoelectric focusing method for specific diagnosis of familial hyperlipoproteinemia type 3.

Authors:  G R Warnick; C Mayfield; J J Albers; W R Hazzard
Journal:  Clin Chem       Date:  1979-02       Impact factor: 8.327

2.  Change in very low-, low-, and high-density lipoproteins during lipid lowering (bezafibrate) therapy: studies in type IIA and type IIb hyperlipoproteinaemia.

Authors:  D Gavish; Y Oschry; M Fainaru; S Eisenberg
Journal:  Eur J Clin Invest       Date:  1986-02       Impact factor: 4.686

3.  Lessons from the Helsinki Heart Study. Fibric acid therapy for dyslipidemia.

Authors:  S M Grundy
Journal:  Postgrad Med       Date:  1988-07       Impact factor: 3.840

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Authors:  K Carlson
Journal:  J Clin Pathol Suppl (Assoc Clin Pathol)       Date:  1973

Review 5.  Classification of hyperlipidaemias and hyperlipoproteinaemias.

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Journal:  Bull World Health Organ       Date:  1970       Impact factor: 9.408

Review 6.  Lipoprotein abnormalities in hypertriglyceridemia: significance in atherosclerosis.

Authors:  S Eisenberg
Journal:  Am Heart J       Date:  1987-02       Impact factor: 4.749

7.  Influence of bezafibrate, fenofibrate, nicotinic acid and etofibrate on plasma high-density lipoprotein levels.

Authors:  R Paoletti; G Franceschini; C R Sirtori
Journal:  Am J Cardiol       Date:  1983-08-22       Impact factor: 2.778

Review 8.  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

9.  Comparison of gemfibrozil and clofibrate on serum lipids in familial combined hyperlipidemia. A randomized placebo-controlled, double-blind, crossover clinical trial.

Authors:  S W Rabkin; M Hayden; J Frohlich
Journal:  Atherosclerosis       Date:  1988-10       Impact factor: 5.162

Review 10.  Bezafibrate. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hyperlipidaemia.

Authors:  J P Monk; P A Todd
Journal:  Drugs       Date:  1987-06       Impact factor: 9.546

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  6 in total

Review 1.  Pharmacological treatment and therapeutic perspectives of metabolic syndrome.

Authors:  Soo Lim; Robert H Eckel
Journal:  Rev Endocr Metab Disord       Date:  2014-12       Impact factor: 6.514

2.  Bezafibrate induces acyl-CoA oxidase mRNA levels and fatty acid peroxisomal beta-oxidation in rat white adipose tissue.

Authors:  M Vázquez; N Roglans; A Cabrero; C Rodríguez; T Adzet; M Alegret; R M Sánchez; J C Laguna
Journal:  Mol Cell Biochem       Date:  2001-01       Impact factor: 3.396

Review 3.  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

4.  Differential effects of fibrates on the acyl composition of microsomal phospholipids in rats.

Authors:  M Vázquez; S Muñoz; M Alegret; T Adzet; M Merlos; J C Laguna
Journal:  Br J Pharmacol       Date:  1995-10       Impact factor: 8.739

5.  Relationship between plasma lipids and palmitoyl-CoA hydrolase and synthetase activities with peroxisomal proliferation in rats treated with fibrates.

Authors:  M Alegret; R Ferrando; M Vázquez; T Adzet; M Merlos; J C Laguna
Journal:  Br J Pharmacol       Date:  1994-06       Impact factor: 8.739

Review 6.  Gemfibrozil. A reappraisal of its pharmacological properties and place in the management of dyslipidaemia.

Authors:  C M Spencer; L B Barradell
Journal:  Drugs       Date:  1996-06       Impact factor: 9.546

  6 in total

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