Literature DB >> 7225166

Fenofibrate therapy of hyperlipoproteinaemia. A dose-response study and a comparison with clofibrate.

S Rössner, L Orö.   

Abstract

Fenofibrate is an efficient serum lipid-lowering drug with few clinical side effects. The drug was further evaluated in a study comprising 56 patients, which combined a dose-response trial with a subsequent comparison between the optimal fenofibrate dose and a clofibrate dose of 2 g/day. When the fenofibrate dose was gradually increased (200-300-400 mg/day), a reduction of the elevated lipoproteins within each type of hyperlipoproteinaemia was found. During the dose-response part of the therapy a transient serum creatinine rise was observed, which disappeared at the 400 mg/day level. The highest dose, 400 mg/day, proved to have the best lipid-lower effects. On this therapy the elevated LDL-cholesterol fell by 28% in type IIA + B patients, and the elevated VLDL-TG by 65% in type IIB + IV patients. The HDL/VLDL + LDL-cholesterol ratio increased significantly in all groups, in particular in type IV patients (from 0.19 to 0.28, P less than 0.001). Fenofibrate and clofibrate were each given for 2 months in random order, and the effects on lipoproteins compared. Significant differences were: higher HDL-cholesterol in type IIA on clofibrate, lower LDL-cholesterol in type IIB on fenofibrate, lower TG and cholesterol in both VLDL an LDL in type IV on fenofibrate, combined with higher HDL-cholesterol on this drug. Thus, fenofibrate seems to be an efficient lipid lowering drug with 400 mg/day as an optimal dosage under our conditions.

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Year:  1981        PMID: 7225166     DOI: 10.1016/0021-9150(81)90043-5

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


  8 in total

Review 1.  Fenofibrate. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in dyslipidaemia.

Authors:  J A Balfour; D McTavish; R C Heel
Journal:  Drugs       Date:  1990-08       Impact factor: 9.546

Review 2.  Lipid-lowering drugs. An overview of indications and optimum therapeutic use.

Authors:  D R Illingworth
Journal:  Drugs       Date:  1987-03       Impact factor: 9.546

3.  Effect of a single daily dose treatment of fenofibrate on plasma lipoproteins in hyperlipoproteinaemia IIb.

Authors:  S Bertolini; N Elicio; A Daga; M L Degl'Innocenti; R Balestreri; M G Fusi; A M Cotta Ramusino; A Carozzi
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

4.  Pharmacokinetics of cyclosporine in hyperlipidaemic long-term survivors of heart transplantation. Lack of interaction with the lipid-lowering agent, fenofibrate.

Authors:  M deLorgeril; P Boissonnat; C A Bizollon; J Guidollet; G Faucon; J P Guichard; R Levy-Prades-Sauron; S Renaud; G Dureau
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

5.  Fenofibrate and colestipol: effects on serum and lipoprotein lipids and apolipoproteins in familial hypercholesterolaemia.

Authors:  P Weisweiler; W Merk; B Jacob; P Schwandt
Journal:  Eur J Clin Pharmacol       Date:  1986       Impact factor: 2.953

6.  Reversibility of fenofibrate therapy-induced renal function impairment in ACCORD type 2 diabetic participants.

Authors:  Josyf C Mychaleckyj; Timothy Craven; Uma Nayak; John Buse; John R Crouse; Marshall Elam; Kent Kirchner; Daniel Lorber; Santica Marcovina; William Sivitz; Joann Sperl-Hillen; Denise E Bonds; Henry N Ginsberg
Journal:  Diabetes Care       Date:  2012-03-19       Impact factor: 19.112

7.  Effect of Fenofibrate Medication on Renal Function.

Authors:  Sungjong Kim; Kyungjin Ko; Sookyoung Park; Dong Ryul Lee; Jungun Lee
Journal:  Korean J Fam Med       Date:  2017-07-20

8.  Effect of fenofibrate on uric acid level in patients with gout.

Authors:  Ju-Yang Jung; Young Choi; Chang-Hee Suh; Dukyong Yoon; Hyoun-Ah Kim
Journal:  Sci Rep       Date:  2018-11-13       Impact factor: 4.379

  8 in total

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