Literature DB >> 12482562

Micronized fenofibrate normalizes the enhanced lipidemic response to a fat load in patients with type 2 diabetes and optimal glucose control.

Elisabeth Cavallero1, Christiane Dachet, Farideh Assadolahi, Claude Martin, Nicole Navarro, Jean-Claude Ansquer, Christophe Corda, Christelle Foucher, Irene Juhan-Vague, Bernard Jacotot.   

Abstract

This study evaluated the postprandial (PP) response to an oral fat load in 28 male patients with type 2 diabetes (mean HbA1c of 5.1%), all receiving metformin and performing physical exercise, compared with healthy subjects. The effects of micronized fenofibrate (200 mg once daily) on triglycerides (TG) and retinyl palmitate (RP) responses, lipoprotein mass concentrations, post-heparin lipase activities and coagulation factors were investigated after a 16-week double-blind, placebo-controlled period. Higher and delayed TG response after the oral fat load (P<0.001) corresponding to increases in both intestinally and endogenous TG-rich lipoproteins and lower lipoprotein lipase (LPL) activity 30 and 60 min post-heparin injection (P<0.05) were observed in the patients as compared with controls. Fasting PAI-1 activity, 6 h PP Factor VII and PAI-1 activities were higher in patients (P=0.036, P=0.032 and P=0.017, respectively). After fenofibrate treatment, TG and RP responses and peak LPL activity were no more significantly different from controls at baseline. Compared with placebo, fasting TG-rich lipoproteins and HDL(3) mass concentrations were significantly lower and higher, respectively; PP chylomicrons and very low density lipoprotein (VLDL) mass concentrations were lower; fasting and PP fibrinogen levels were significantly reduced after fenofibrate treatment. Diabetes control was unchanged throughout the study. Fenofibrate normalized the abnormal PP response and improved the fasting lipoprotein abnormalities in patients with type 2 diabetes and optimal glucose control.

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Year:  2003        PMID: 12482562     DOI: 10.1016/s0021-9150(02)00321-0

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


  7 in total

1.  Comment on: Weickert MO, Pfeiffer AFH (2006) Signalling mechanisms linking hepatic glucose and lipid metabolism. Diabetologia 49:1732-1741.

Authors:  R N A Black; P M Bell
Journal:  Diabetologia       Date:  2006-12-06       Impact factor: 10.122

Review 2.  Fenofibrate: a review of its use in primary dyslipidaemia, the metabolic syndrome and type 2 diabetes mellitus.

Authors:  Gillian M Keating; Katherine F Croom
Journal:  Drugs       Date:  2007       Impact factor: 9.546

Review 3.  Fenofibrate: a review of its use in dyslipidaemia.

Authors:  Kate McKeage; Gillian M Keating
Journal:  Drugs       Date:  2011-10-01       Impact factor: 9.546

4.  Association of plasminogen activator inhibitor-1 and tissue plasminogen activator with type 2 diabetes and metabolic syndrome in Malaysian subjects.

Authors:  Zaid Al-Hamodi; Ikram S Ismail; Riyadh Saif-Ali; Khaled A Ahmed; Sekaran Muniandy
Journal:  Cardiovasc Diabetol       Date:  2011-03-18       Impact factor: 9.951

Review 5.  Fibrate therapy in patients with metabolic syndrome and diabetes mellitus.

Authors:  Thomas Dayspring; Gregory Pokrywka
Journal:  Curr Atheroscler Rep       Date:  2006-09       Impact factor: 5.113

6.  Micronized Curcumin Causes Hyperlocomotion in Zebrafish Larvae.

Authors:  Adrieli Sachett; Radharani Benvenutti; Carlos G Reis; Matheus Gallas-Lopes; Leonardo M Bastos; Gean P S Aguiar; Ana P Herrmann; J Vladimir Oliveira; Anna M Siebel; Angelo Piato
Journal:  Neurochem Res       Date:  2022-05-10       Impact factor: 4.414

Review 7.  Fenofibrate: a novel formulation (Triglide) in the treatment of lipid disorders: a review.

Authors:  Konstantinos Tziomalos; Vasilios G Athyros
Journal:  Int J Nanomedicine       Date:  2006
  7 in total

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