Literature DB >> 215174

Dose-response study of bezafibrate on serum lipoprotein concentrations in hyperlipoproteinanemia.

A G Olsson, P D Lang.   

Abstract

The effect of bezafibrate in the dosages 450, 900 and 1350 mg daily on serum lipoprotein concentrations were studied in 20 subjects with primary hyperlipoproteinaemia (16 of type IV, 2 of type II B, 1 of type III). Except for LDL cholesterol maximum effects were obtained with 450 mg daily. Total serum cholesterol and triglycerides (TG) fell significantly. Mean very low density lipoprotein (VLDL) TG fell by 54%. The maximum effect on low density lipoprotein was obtained with 900 mg daily. The effect was highly dependent on initial concentrations, decreases being observed above 4 mmoles/l and increases below that concentration. High density lipoprotein cholesterol increased by 31% (P less than 0.01) independently of the VLDL decrease. Three subjects suffered gastrointestinal side-effects on 1350 mg daily. Only benign reversible changes were noted on non-lipid measurements. Bezafibrate is a well-tolerated drug with a good VLDL TG lowering effect. It is particularly effective in increasing HDL cholesterol concentrations.

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Year:  1978        PMID: 215174     DOI: 10.1016/0021-9150(78)90137-5

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


  11 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.  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

3.  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

Review 4.  Use of fibrates in the metabolic syndrome: A review.

Authors:  Kate E Shipman; Richard C Strange; Sudarshan Ramachandran
Journal:  World J Diabetes       Date:  2016-03-10

5.  Stimulation of decreased lipoprotein lipase activity in the tumor-bearing state by the antihyperlipidemic drug bezafibrate.

Authors:  K Nomura; Y Noguchi; A Matsumoto
Journal:  Surg Today       Date:  1996       Impact factor: 2.549

6.  [Relation between serum lipoprotein metabolism and biliary lipid metabolism].

Authors:  O Leiss; K von Bergmann
Journal:  Klin Wochenschr       Date:  1983-06-15

Review 7.  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

8.  The PPAR pan-agonist bezafibrate ameliorates cardiomyopathy in a mouse model of Barth syndrome.

Authors:  Yan Huang; Corey Powers; Victoria Moore; Caitlin Schafer; Mindong Ren; Colin K L Phoon; Jeanne F James; Alexander V Glukhov; Sabzali Javadov; Frédéric M Vaz; John L Jefferies; Arnold W Strauss; Zaza Khuchua
Journal:  Orphanet J Rare Dis       Date:  2017-03-09       Impact factor: 4.123

Review 9.  Elucidating the Beneficial Role of PPAR Agonists in Cardiac Diseases.

Authors:  Zaza Khuchua; Aleksandr I Glukhov; Arnold W Strauss; Sabzali Javadov
Journal:  Int J Mol Sci       Date:  2018-11-04       Impact factor: 5.923

10.  Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan.

Authors:  Kenji Yamada; Hideaki Shiraishi; Eishin Oki; Mika Ishige; Toshiyuki Fukao; Yusuke Hamada; Norio Sakai; Fumihiro Ochi; Asami Watanabe; Sanae Kawakami; Kazuyo Kuzume; Kenji Watanabe; Koji Sameshima; Kiyotaka Nakamagoe; Akira Tamaoka; Naoko Asahina; Saki Yokoshiki; Takashi Miyakoshi; Kota Ono; Koji Oba; Toshiyuki Isoe; Hiroshi Hayashi; Seiji Yamaguchi; Norihiro Sato
Journal:  Mol Genet Metab Rep       Date:  2018-02-22
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