Effects of a bezafibrate sustained release formulation on plasma lipoproteins in patients with hypercholesterolemia. Importance of timing of tablet intake for efficacy

Arzneimittelforschung. 1988 Dec;38(12):1835-7.

Abstract

The therapeutic effect of a single sustained release tablet of bezafibrate (Cedur retard, 400 mg) in primary hypercholesterolemia type IIa and type IIb was investigated in a placebo-controlled randomised study comparing the efficacy of morning vs. evening intake. The decrease in total cholesterol with the morning intake was 18.5% vs. 16.5% for the evening intake (n.s.). HDL-cholesterol increased more in patients taking bezafibrate retard at morning (29.6% vs. 22.4%, p less than 0.05). Bezafibrate was well tolerated. Animal experiments and precursor studies of cholesterol synthesis in man indicate peak activity of HMG-CoA reductase between 1 a.m. and 3 a.m. The data suggest that with normal eating habits during day time other modes of action of bezafibrate besides HMG-CoA reductase inhibition such as reduction of VLDL-synthesis in the liver and an increased fractional catabolic rate, could contribute to the therapeutic effect.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Alkaline Phosphatase / blood
  • Apolipoproteins A / blood
  • Bezafibrate / administration & dosage
  • Bezafibrate / therapeutic use*
  • Delayed-Action Preparations
  • Female
  • Humans
  • Hypercholesterolemia / blood
  • Hypercholesterolemia / drug therapy*
  • Lipids / blood
  • Lipoproteins / blood*
  • Male
  • Middle Aged
  • Time Factors

Substances

  • Apolipoproteins A
  • Delayed-Action Preparations
  • Lipids
  • Lipoproteins
  • Alkaline Phosphatase
  • Bezafibrate