Literature DB >> 21942979

Fenofibrate: a review of its use in dyslipidaemia.

Kate McKeage1, Gillian M Keating.   

Abstract

Fenofibrate is a fibric acid derivative indicated for the treatment of severe hypertriglyceridaemia and mixed dyslipidaemia in patients who have not responded to nonpharmacological therapies. The lipid-modifying effects of fenofibrate are mediated by the activation of peroxisome proliferator-activated receptor-α. Fenofibrate also has nonlipid, pleiotropic effects (e.g. reducing levels of fibrinogen, C-reactive protein and various pro-inflammatory markers, and improving flow-mediated dilatation) that may contribute to its clinical efficacy, particularly in terms of improving microvascular outcomes. Fenofibrate improves the lipid profile (particularly triglyceride [TG] and high-density lipoprotein-cholesterol [HDL-C] levels) in patients with dyslipidaemia. Compared with statin monotherapy, fenofibrate monotherapy tends to improve TG and HDL-C levels to a significantly greater extent, whereas statins improve low-density lipoprotein-cholesterol (LDL-C) and total cholesterol levels to a significantly greater extent. Fenofibrate is also associated with promoting a shift from small, dense, atherogenic LDL particles to larger, less dense LDL particles. Combination therapy with a statin plus fenofibrate generally improves the lipid profile to a greater extent than monotherapy with either agent in patients with dyslipidaemia and/or type 2 diabetes mellitus or the metabolic syndrome. In the pivotal FIELD and ACCORD trials in patients with type 2 diabetes, fenofibrate did not significantly reduce the risk of coronary heart disease events to a greater extent than placebo, and simvastatin plus fenofibrate did not significantly reduce the risk of major cardiovascular (CV) events to a greater extent than simvastatin plus placebo. However, the risk of some nonfatal macrovascular events and the incidence of certain microvascular outcomes were reduced significantly more with fenofibrate than with placebo in the FIELD trial, and in the ACCORD trial, patients receiving simvastatin plus fenofibrate were less likely to experience progression of diabetic retinopathy than those receiving simvastatin plus placebo. Subgroup analyses in the FIELD and ACCORD Lipid trials indicate that fenofibrate is of the greatest benefit in decreasing CV events in patients with atherogenic dyslipidaemia. Fenofibrate is generally well tolerated when administered alone or in combination with a statin. Thus, in patients with dyslipidaemia, particularly atherogenic dyslipidaemia, fenofibrate is a useful treatment option either alone or in combination with a statin.

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Year:  2011        PMID: 21942979     DOI: 10.2165/11208090-000000000-00000

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


  168 in total

1.  Attenuation of progression of insulin resistance in patients with coronary artery disease by bezafibrate.

Authors:  Alexander Tenenbaum; Enrique Z Fisman; Valentina Boyko; Michal Benderly; David Tanne; Moti Haim; Zipora Matas; Michael Motro; Solomon Behar
Journal:  Arch Intern Med       Date:  2006-04-10

2.  European guidelines on cardiovascular disease prevention in clinical practice: full text. Fourth Joint Task Force of the European Society of Cardiology and other societies on cardiovascular disease prevention in clinical practice (constituted by representatives of nine societies and by invited experts).

Authors:  Ian Graham; Dan Atar; Knut Borch-Johnsen; Gudrun Boysen; Gunilla Burell; Renata Cifkova; Jean Dallongeville; Guy De Backer; Shah Ebrahim; Bjørn Gjelsvik; Christoph Herrmann-Lingen; Arno Hoes; Steve Humphries; Mike Knapton; Joep Perk; Silvia G Priori; Kalevi Pyorala; Zeljko Reiner; Luis Ruilope; Susana Sans-Menendez; Wilma Scholte Op Reimer; Peter Weissberg; David Wood; John Yarnell; Jose Luis Zamorano; Edmond Walma; Tony Fitzgerald; Marie Therese Cooney; Alexandra Dudina; Alec Vahanian; John Camm; Raffaele De Caterina; Veronica Dean; Kenneth Dickstein; Christian Funck-Brentano; Gerasimos Filippatos; Irene Hellemans; Steen Dalby Kristensen; Keith McGregor; Udo Sechtem; Sigmund Silber; Michal Tendera; Petr Widimsky; Jóse Luis Zamorano; Attila Altiner; Enzo Bonora; Paul N Durrington; Robert Fagard; Simona Giampaoli; Harry Hemingway; Jan Hakansson; Sverre Erik Kjeldsen; mogens Lytken Larsen; Giuseppe Mancia; Athanasios J Manolis; Kristina Orth-Gomer; Terje Pedersen; Mike Rayner; Lars Ryden; Mario Sammut; Neil Schneiderman; Anton F Stalenhoef; Lale Tokgözoglu; Olov Wiklund; Antonis Zampelas
Journal:  Eur J Cardiovasc Prev Rehabil       Date:  2007-09

3.  Effects of combination lipid therapy in the management of patients with type 2 diabetes mellitus in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.

Authors:  Andrew M Tonkin; Lei Chen
Journal:  Circulation       Date:  2010-08-24       Impact factor: 29.690

4.  Fenofibrate suppresses microvascular inflammation and apoptosis through adenosine monophosphate-activated protein kinase activation.

Authors:  Atsuko Tomizawa; Yoshiyuki Hattori; Teruo Inoue; Sachiko Hattori; Kikuo Kasai
Journal:  Metabolism       Date:  2010-06-26       Impact factor: 8.694

5.  Safety and efficacy of colesevelam hydrochloride in combination with fenofibrate for the treatment of mixed hyperlipidemia.

Authors:  James McKenney; Michael Jones; Stacey Abby
Journal:  Curr Med Res Opin       Date:  2005-09       Impact factor: 2.580

Review 6.  Modulation of hepatic inflammatory risk markers of cardiovascular diseases by PPAR-alpha activators: clinical and experimental evidence.

Authors:  Alberto Zambon; Philippe Gervois; Paolo Pauletto; Jean-Charles Fruchart; Bart Staels
Journal:  Arterioscler Thromb Vasc Biol       Date:  2006-01-19       Impact factor: 8.311

7.  Effect of colesevelam HCl on single-dose fenofibrate pharmacokinetics.

Authors:  Michael R Jones; Brian A Baker; Philip Mathew
Journal:  Clin Pharmacokinet       Date:  2004       Impact factor: 6.447

8.  Effect of fenofibrate on the need for laser treatment for diabetic retinopathy (FIELD study): a randomised controlled trial.

Authors:  A C Keech; P Mitchell; P A Summanen; J O'Day; T M E Davis; M S Moffitt; M-R Taskinen; R J Simes; D Tse; E Williamson; A Merrifield; L T Laatikainen; M C d'Emden; D C Crimet; R L O'Connell; P G Colman
Journal:  Lancet       Date:  2007-11-07       Impact factor: 79.321

9.  Simvastatin does not have a clinically significant pharmacokinetic interaction with fenofibrate in humans.

Authors:  Arthur J Bergman; Gail Murphy; Joanne Burke; Jamie J Zhao; Robert Valesky; Lida Liu; Kenneth C Lasseter; Weili He; Thomayant Prueksaritanont; Yue Qiu; Alan Hartford; Jose M Vega; John F Paolini
Journal:  J Clin Pharmacol       Date:  2004-09       Impact factor: 3.126

Review 10.  Update on the clinical utility of fenofibrate in mixed dyslipidemias: mechanisms of action and rational prescribing.

Authors:  Michel Farnier
Journal:  Vasc Health Risk Manag       Date:  2008
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  36 in total

1.  The peroxisomal proliferator-activated receptor (PPAR) α agonist, fenofibrate, prevents fractionated whole-brain irradiation-induced cognitive impairment.

Authors:  Dana Greene-Schloesser; Valerie Payne; Ann M Peiffer; Fang-Chi Hsu; David R Riddle; Weiling Zhao; Michael D Chan; Linda Metheny-Barlow; Mike E Robbins
Journal:  Radiat Res       Date:  2014-01-07       Impact factor: 2.841

2.  Current practice in identifying and treating cardiovascular risk, with a focus on residual risk associated with atherogenic dyslipidaemia.

Authors:  Roberto Ferrari; Carlos Aguiar; Eduardo Alegria; Riccardo C Bonadonna; Francesco Cosentino; Moses Elisaf; Michel Farnier; Jean Ferrières; Pasquale Perrone Filardi; Nicolae Hancu; Meral Kayikcioglu; Alberto Mello E Silva; Jesus Millan; Željko Reiner; Lale Tokgozoglu; Paul Valensi; Margus Viigimaa; Michal Vrablik; Alberto Zambon; José Luis Zamorano; Alberico L Catapano
Journal:  Eur Heart J Suppl       Date:  2016-04-12       Impact factor: 1.803

3.  Modulation of the IL-23/IL-17 axis by fenofibrate ameliorates the ovalbumin/lipopolysaccharide-induced airway inflammation and bronchial asthma in rats.

Authors:  Samah M Elaidy; Soha S Essawy; Mona A Hussain; Mohamed K El-Kherbetawy; Eman R Hamed
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2017-12-30       Impact factor: 3.000

Review 4.  Radiation-induced cognitive impairment--from bench to bedside.

Authors:  Dana Greene-Schloesser; Mike E Robbins
Journal:  Neuro Oncol       Date:  2012-09       Impact factor: 12.300

5.  PPARα agonist fenofibrate enhances fatty acid β-oxidation and attenuates polycystic kidney and liver disease in mice.

Authors:  Ronak Lakhia; Matanel Yheskel; Andrea Flaten; Ezekiel B Quittner-Strom; William L Holland; Vishal Patel
Journal:  Am J Physiol Renal Physiol       Date:  2017-09-13

6.  Upregulation of hepatic VLDLR via PPARα is required for the triglyceride-lowering effect of fenofibrate.

Authors:  Yang Gao; Wei Shen; Boyu Lu; Qingjiong Zhang; Yang Hu; Ying Chen
Journal:  J Lipid Res       Date:  2014-06-04       Impact factor: 5.922

7.  Fenofibrate unexpectedly induces cardiac hypertrophy in mice lacking MuRF1.

Authors:  Traci L Parry; Gopal Desai; Jonathan C Schisler; Luge Li; Megan T Quintana; Natalie Stanley; Pamela Lockyer; Cam Patterson; Monte S Willis
Journal:  Cardiovasc Pathol       Date:  2015-10-29       Impact factor: 2.185

Review 8.  Pathological changes in the central nervous system following exposure to ionizing radiation.

Authors:  S Bálentová; M Adamkov
Journal:  Physiol Res       Date:  2020-05-29       Impact factor: 1.881

9.  Radiation-induced brain injury: A review.

Authors:  Dana Greene-Schloesser; Mike E Robbins; Ann M Peiffer; Edward G Shaw; Kenneth T Wheeler; Michael D Chan
Journal:  Front Oncol       Date:  2012-07-19       Impact factor: 6.244

10.  Dietary Fructus Schisandrae extracts and fenofibrate regulate the serum/hepatic lipid-profile in normal and hypercholesterolemic mice, with attention to hepatotoxicity.

Authors:  Si-Yuan Pan; Qing Yu; Yi Zhang; Xiao-Yan Wang; Nan Sun; Zhi-Ling Yu; Kam-Ming Ko
Journal:  Lipids Health Dis       Date:  2012-09-19       Impact factor: 3.876

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