Literature DB >> 901625

Effect of BM 15.075 on lipoprotein concentrations in different types of hyperlipoproteinaemia.

A G Olsson, S Rössner, G Walldius, L A Carlson, P D Lang.   

Abstract

The four-week lipoprotein lowering effect of 0.2 g t.i.d. of BM 15.075 and of 0.5 g t.i.d. of clofibrate was studied in 29 subjects with different types of hyperlipoproteinaemia in a single blind crossover fashion. BM 15.075 decreased very low density lipoproteins (VLDL), triglycerides (TG) and cholesterol concentration in all types of hyperlipoproteinaemia the effect being dependent on initial lipoprotein concentrations. BM 15.075 decreased VLDL triglyceride concentrations on average 20% more than did clofibrate. BM 15.075 decreased low density lipoproteins (LDL) cholesterol concentrations in Type IIA and IIB but did not significantly affect this lipoprotein lipid in type IV hyperlipoproteinaemia. Regression analysis showed that the drug tended to decrease LDL cholesterol if initial concentrations were above 157 mg/100 ml and to increase initially lower levels. No significant differences between BM 15.075 and clofibrate was found in the effect of LDL cholesterol. High density lipoproteins (HDL) cholesterol concentrations were not influenced by BM 15.075. No subjective side effects were noted on BM 15.075. S-ASAT increased and alcaline phosphatases decreased on both treatments.

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Year:  1977        PMID: 901625     DOI: 10.1016/0021-9150(77)90037-5

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  12 in total

1.  Steady-state kinetics of bezafibrate retard in hyperlipidemic geriatric patients.

Authors:  G Neugebauer; D Platt; T Vömel; W Lösch
Journal:  Klin Wochenschr       Date:  1988-03-15

2.  Apolipoprotein A and B (Sf 100-400) metabolism during bezafibrate therapy in hypertriglyceridemic subjects.

Authors:  J Shepherd; C J Packard; J M Stewart; R F Atmeh; R S Clark; D E Boag; K Carr; A R Lorimer; D Ballantyne; H G Morgan
Journal:  J Clin Invest       Date:  1984-12       Impact factor: 14.808

3.  Pharmacokinetics of bezafibrate after single and multiple doses in the presence of renal failure.

Authors:  U Abshagen; W Kösters; B Kaufmann; P D Lang
Journal:  Klin Wochenschr       Date:  1980-09-01

4.  Disposition pharmacokinetics of bezafibrate in man.

Authors:  U Abshagen; W Bablok; K Koch; P D Lang; H A Schmidt; M Senn; H Stork
Journal:  Eur J Clin Pharmacol       Date:  1979-08       Impact factor: 2.953

5.  Differences in the response of Sprague-Dawley and Lewis rats to bezafibrate: the hypolipidemic effect and the induction of peroxisomal enzymes.

Authors:  J Pill; A Völkl; F Hartig; H D Fahimi
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

6.  Effects of clofibrate, bezafibrate, fenofibrate and probucol on plasma lipolytic enzymes in normolipaemic subjects.

Authors:  F Heller; C Harvengt
Journal:  Eur J Clin Pharmacol       Date:  1983       Impact factor: 2.953

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

Review 8.  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

9.  Clinical pharmacokinetics of bezafibrate in patients with impaired renal function.

Authors:  P Anderson; H E Norbeck
Journal:  Eur J Clin Pharmacol       Date:  1981       Impact factor: 2.953

10.  [Bezafibrate in primary hyperlipidemias (author's transl)].

Authors:  J G Wechsler; V Hutt; H U Klör; G Bode; H Ditschuneit
Journal:  Klin Wochenschr       Date:  1982-01-15
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