Literature DB >> 11122722

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

M F Linton1, S Fazio.   

Abstract

It is now widely accepted that low-density lipoprotein (LDL) is not the only atherogenic component of the lipid profile and that abnormalities in the metabolism and plasma levels of triglycerides and high-density lipoprotein (HDL) may lead to accelerated growth of atherosclerotic lesions. Fibrates are the drugs of first choice in the management of hypertriglyceridemia, and are also able to substantially raise HDL. The recently published Veterans Administration-High-density Lipoprotein Intervention Trial (VA-HIT) trial showed that fibrate treatment in patients with coronary heart disease (CHD), low HDL, modestly elevated triglycerides, and normal LDL reduces the risk of a recurrent coronary event by 25%. A reasonable approach to the dyslipidemic patient with high CHD risk is to tailor the intervention to the specific lipoprotein abnormality. Under these assumptions fibrate therapy should become widespread, considering that the most common lipid alteration in CHD and patients with diabetes is low HDL and high triglycerides.

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Year:  2000        PMID: 11122722     DOI: 10.1007/s11883-000-0092-2

Source DB:  PubMed          Journal:  Curr Atheroscler Rep        ISSN: 1523-3804            Impact factor:   5.967


  46 in total

1.  PPARalpha and PPARgamma activators direct a distinct tissue-specific transcriptional response via a PPRE in the lipoprotein lipase gene.

Authors:  K Schoonjans; J Peinado-Onsurbe; A M Lefebvre; R A Heyman; M Briggs; S Deeb; B Staels; J Auwerx
Journal:  EMBO J       Date:  1996-10-01       Impact factor: 11.598

2.  Fenofibrate reduces plasma cholesteryl ester transfer from HDL to VLDL and normalizes the atherogenic, dense LDL profile in combined hyperlipidemia.

Authors:  M Guérin; E Bruckert; P J Dolphin; G Turpin; M J Chapman
Journal:  Arterioscler Thromb Vasc Biol       Date:  1996-06       Impact factor: 8.311

3.  Multicenter comparison of micronized fenofibrate and simvastatin in patients with primary type IIA or IIB hyperlipoproteinemia.

Authors:  A Steinmetz; T Schwartz; U Hehnke; H Kaffarnik
Journal:  J Cardiovasc Pharmacol       Date:  1996-04       Impact factor: 3.105

4.  Comparison of the efficacy and safety of fenofibrate and lovastatin in patients with primary type IIa or IIb hyperlipidaemia.

Authors:  K Gholami; N Tavakoli; M Maleki; A Shafiee
Journal:  J Clin Pharm Ther       Date:  1998-06       Impact factor: 2.512

5.  Lipid alterations and decline in the incidence of coronary heart disease in the Helsinki Heart Study.

Authors:  V Manninen; M O Elo; M H Frick; K Haapa; O P Heinonen; P Heinsalmi; P Helo; J K Huttunen; P Kaitaniemi; P Koskinen
Journal:  JAMA       Date:  1988-08-05       Impact factor: 56.272

6.  Effects of monotherapy with an HMG-CoA reductase inhibitor on the progression of coronary atherosclerosis as assessed by serial quantitative arteriography. The Canadian Coronary Atherosclerosis Intervention Trial.

Authors:  D Waters; L Higginson; P Gladstone; B Kimball; M Le May; S J Boccuzzi; J Lespérance
Journal:  Circulation       Date:  1994-03       Impact factor: 29.690

7.  Reduction of mortality in the Stockholm Ischaemic Heart Disease Secondary Prevention Study by combined treatment with clofibrate and nicotinic acid.

Authors:  L A Carlson; G Rosenhamer
Journal:  Acta Med Scand       Date:  1988

8.  Activation of human aortic smooth-muscle cells is inhibited by PPARalpha but not by PPARgamma activators.

Authors:  B Staels; W Koenig; A Habib; R Merval; M Lebret; I P Torra; P Delerive; A Fadel; G Chinetti; J C Fruchart; J Najib; J Maclouf; A Tedgui
Journal:  Nature       Date:  1998-06-25       Impact factor: 49.962

9.  Fibrates downregulate apolipoprotein C-III expression independent of induction of peroxisomal acyl coenzyme A oxidase. A potential mechanism for the hypolipidemic action of fibrates.

Authors:  B Staels; N Vu-Dac; V A Kosykh; R Saladin; J C Fruchart; J Dallongeville; J Auwerx
Journal:  J Clin Invest       Date:  1995-02       Impact factor: 14.808

10.  Effects of lipid lowering by pravastatin on progression and regression of coronary artery disease in symptomatic men with normal to moderately elevated serum cholesterol levels. The Regression Growth Evaluation Statin Study (REGRESS).

Authors:  J W Jukema; A V Bruschke; A J van Boven; J H Reiber; E T Bal; A H Zwinderman; H Jansen; G J Boerma; F M van Rappard; K I Lie
Journal:  Circulation       Date:  1995-05-15       Impact factor: 29.690

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  4 in total

Review 1.  Correction of dysfunctional fatty acid metabolism using peroxisome proliferator activated receptor gamma agonists.

Authors:  Nicholas D Oakes; Bengt Ljung; Germán Camejo
Journal:  J R Soc Med       Date:  2002       Impact factor: 5.344

Review 2.  Signalling mechanisms linking hepatic glucose and lipid metabolism.

Authors:  M O Weickert; A F H Pfeiffer
Journal:  Diabetologia       Date:  2006-05-23       Impact factor: 10.122

Review 3.  PPAR ligands: potential therapies for metabolic syndrome.

Authors:  Taro E Akiyama; Peter T Meinke; Joel P Berger
Journal:  Curr Diab Rep       Date:  2005-02       Impact factor: 4.810

4.  Clofibrate-induced changes in the liver, heart, brain and white adipose lipid metabolome of Swiss-Webster mice.

Authors:  Craig E Wheelock; Susumu Goto; Bruce D Hammock; John W Newman
Journal:  Metabolomics       Date:  2007-06       Impact factor: 4.290

  4 in total

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