Literature DB >> 8736620

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

C M Spencer1, L B Barradell.   

Abstract

Gemfibrozil improves lipid and apolipoprotein profiles, particularly very low density lipoprotein (VLDL) triglyceride and high density lipoprotein (HDL) cholesterol levels, in patients with dyslipidaemia when administered at a total daily dose of 900 or 1200 mg. As demonstrated by the Helsinki Heart Study, these effects result in a reduction in some risk factors for coronary heart disease (CHD) and also a 34% reduction in the incidence of this disease after 5 years compared with placebo. Limited data suggest that gemfibrozil has beneficial effects on the fibrinolytic system and may slow the progression of atherosclerosis. Gemfibrozil has shown efficacy in the treatment of patients with type IIa, IIb, III, IV or V dyslipidaemia or hypoalphalipoproteinaemia, especially in patients with elevated triglyceride and low HDL cholesterol levels. It is also effective in patients with non-insulin-dependent diabetes mellitus (NIDDM) and dyslipidaemia and has no detrimental effects on glycaemic control. A small number of studies also showed gemfibrozil to be effective for the control of dyslipidaemia associated with renal failure, transplantation, nephrotic syndrome, arterial occlusive disease or systemic lupus erythematosus. However, patients with pre-existing CHD do not appear to derive the same benefits (reduced CHD mortality) from gemfibrozil therapy as these other patients, although results are based on studies of limited size and number. In general, gemfibrozil has at least similar efficacy to bile acid sequestrants and other fibric acid derivatives. Comparisons with HMG-CoA reductase inhibitors show these agents to produce different effects on lipid profiles from gemfibrozil. Thus, gemfibrozil would be expected to be superior in some patients (those with elevated triglyceride or VLDL cholesterol levels), but HMG-CoA reductase inhibitors should have greater benefits in those with elevated low density lipoprotein cholesterol levels. Thus, in patients with elevated triglyceride levels and low HDL cholesterol levels, and, particularly in patients with NIDDM, gemfibrozil is a useful treatment option, which has been shown to reduce the risk of CHD in middle aged men. However, limited available data prevents the accurate comparison of this agent with HMG-CoA reductase inhibitors in patients with this lipid profile.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8736620     DOI: 10.2165/00003495-199651060-00009

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  166 in total

1.  Efficacy and cost-effectiveness of simvastatin and gemfibrozil in the treatment of hyperlipidaemia.

Authors:  M C Lim; W M Foo
Journal:  Ann Acad Med Singapore       Date:  1992-01       Impact factor: 2.473

2.  Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge.

Authors:  W T Friedewald; R I Levy; D S Fredrickson
Journal:  Clin Chem       Date:  1972-06       Impact factor: 8.327

3.  Predictive value for coronary heart disease of baseline high-density and low-density lipoprotein cholesterol among Fredrickson type IIa subjects in the Helsinki Heart Study.

Authors:  V Manninen; P Koskinen; M Manttari; J K Huttunen; D Canter; H M Frick
Journal:  Am J Cardiol       Date:  1990-09-04       Impact factor: 2.778

Review 4.  Management of primary hyperlipidemia.

Authors:  R J Havel; E Rapaport
Journal:  N Engl J Med       Date:  1995-06-01       Impact factor: 91.245

Review 5.  Gemfibrozil-induced myopathy.

Authors:  G J Magarian; L M Lucas; C Colley
Journal:  Arch Intern Med       Date:  1991-09

6.  Gemfibrozil treatment of the high triglyceride-low high-density lipoprotein cholesterol trait in men with established atherosclerosis.

Authors:  H C Knipscheer; M T Nurmohamed; A Van den Ende; B Plaat; H J Pruijs; W J Mulder; J J Kastelein
Journal:  J Intern Med       Date:  1994-10       Impact factor: 8.989

7.  Changes in composition and distribution of LDL subspecies in hypertriglyceridemic and hypercholesterolemic patients during gemfibrozil therapy.

Authors:  J Yuan; M Y Tsai; D B Hunninghake
Journal:  Atherosclerosis       Date:  1994-09-30       Impact factor: 5.162

8.  Comparison of the efficacy of simvastatin and standard fibrate therapy in the treatment of primary hypercholesterolemia and combined hyperlipidemia.

Authors:  E Bruckert; J L De Gennes; W Malbecq; F Baigts
Journal:  Clin Cardiol       Date:  1995-11       Impact factor: 2.882

9.  Gemfibrozil treatment is associated with elevated adrenal androgen, androstanediol glucuronide and cortisol levels in dyslipidemic men.

Authors:  A Hautanen; M Mänttäri; V Manninen; H Adlercreutz
Journal:  J Steroid Biochem Mol Biol       Date:  1994-12       Impact factor: 4.292

10.  Coronary heart disease incidence in NIDDM patients in the Helsinki Heart Study.

Authors:  P Koskinen; M Mänttäri; V Manninen; J K Huttunen; O P Heinonen; M H Frick
Journal:  Diabetes Care       Date:  1992-07       Impact factor: 19.112

View more
  10 in total

1.  Photodegradation of gemfibrozil in aqueous solution under UV irradiation: kinetics, mechanism, toxicity, and degradation pathways.

Authors:  Jingshuai Ma; Wenying Lv; Ping Chen; Yida Lu; Fengliang Wang; Fuhua Li; Kun Yao; Guoguang Liu
Journal:  Environ Sci Pollut Res Int       Date:  2016-04-07       Impact factor: 4.223

Review 2.  Micronised fenofibrate: a review of its pharmacodynamic properties and clinical efficacy in the management of dyslipidaemia.

Authors:  J C Adkins; D Faulds
Journal:  Drugs       Date:  1997-10       Impact factor: 9.546

3.  Gemfibrozil modulates cytochrome P450 and peroxisome proliferation-inducible enzymes in the liver of the yellow European eel (Anguilla anguilla).

Authors:  Angeliki Lyssimachou; Rémi Thibaut; Enric Gisbert; Cinta Porte
Journal:  Environ Sci Pollut Res Int       Date:  2013-07-05       Impact factor: 4.223

Review 4.  Clinical positioning of HMG-CoA reductase inhibitors in lipid management protocols.

Authors:  M Cziraky
Journal:  Pharmacoeconomics       Date:  1998       Impact factor: 4.981

5.  A comparison of the use, effectiveness and safety of bezafibrate, gemfibrozil and simvastatin in normal clinical practice using the New Zealand Intensive Medicines Monitoring Programme (IMMP).

Authors:  P W Beggs; D W Clark; S M Williams; D M Coulter
Journal:  Br J Clin Pharmacol       Date:  1999-01       Impact factor: 4.335

Review 6.  The benefits of niacin in atherosclerosis.

Authors:  S Tavintharan; M L Kashyap
Journal:  Curr Atheroscler Rep       Date:  2001-01       Impact factor: 5.113

Review 7.  The role of fibrates in managing hyperlipidemia: mechanisms of action and clinical efficacy.

Authors:  Sergio Fazio; MacRae F Linton
Journal:  Curr Atheroscler Rep       Date:  2004-03       Impact factor: 5.113

Review 8.  Micronised fenofibrate: an updated review of its clinical efficacy in the management of dyslipidaemia.

Authors:  Gillian M Keating; Douglas Ormrod
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 9.  Re-emergence of fibrates in the management of dyslipidemia and cardiovascular risk.

Authors:  M F Linton; S Fazio
Journal:  Curr Atheroscler Rep       Date:  2000-01       Impact factor: 5.967

10.  Quantitative Prediction of Drug-Drug Interactions Involving Inhibitory Metabolites in Drug Development: How Can Physiologically Based Pharmacokinetic Modeling Help?

Authors:  I E Templeton; Y Chen; J Mao; J Lin; H Yu; S Peters; M Shebley; M V Varma
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2016-09-19
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.