Literature DB >> 15543343

Statin and fibrate treatment of combined hyperlipidemia: the effects on some novel risk factors.

Miran Sebestjen1, Irena Keber, Branka Zegura, Sasa Simcic, Mojca Bozic, Martine Migaud Fressart, Mojca Stegnar.   

Abstract

The effects of cerivastatin and fenofibrate on proteins involved in haemostasis and on markers of inflammation were investigated in otherwise healthy middle-aged males with combined hyperlipidemia. Besides classical risk factors, other so-called novel risk factors for coronary artery disease are seen to be playing an increasingly important role in the development and progression of atherosclerosis. Thirty-eight males, aged 49 +/-5 years were randomised to 12 weeks treatment either with cerivastatin at a daily dose of 0.2 mg to 0.4 mg to achieve the LDL cholesterol goal of <3.0 mM, or with fenofibrate 250 mg daily. Fasting serum lipids, homocysteine, total and free tissue factor pathway inhibitor (TFPI), plasminogen activator inhibitor (PAI-1) and tissue plasminogen activator (t-PA) antigen and activity, C-reactive protein (CRP), interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-alpha) were measured. No change in homocysteine level was observed in the cerivastatin group, while after fenofibrate administration it increased (p <0.0001). Total TFPI decreased significantly after cerivastatin (p = 0.002), but not after fenofibrate. Free TFPI did not decrease after either drug. Neither drug affected (t-PA) antigen and activity, while fenofibrate increased PAI-1 antigen (p <0.05) and activity (p <0.05). Cerivastatin decreased serum CRP values by 49.5% (p = 0.001), and fenofibrate by 29.8% (p = 0.03). The decreases of CRP in the two groups differed significantly (p = 0.04). IL-6 levels decreased significantly in the fenofibrate group (39%; p <0.0001), but not in the cerivastatin group (15%; p = 0.24) No significant decreases were observed for TNF-alpha. Cerivastatin had neutral effects on fibrinolysis, homocysteine or coagulation. On the other hand, fenofibrate increased PAI-1 antigen and activity and homocysteine, and did not affect coagulation. Both cerivastatin and fenofibrate reduced CRP levels, the decrease being significantly greater after cerivastatin. Fenofibrate also significantly decreased IL-6.

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Year:  2004        PMID: 15543343     DOI: 10.1160/TH03-04-0250

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  8 in total

1.  Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.

Authors:  Alexis C Frazier-Wood; Stella Aslibekyan; Ingrid B Borecki; Paul N Hopkins; Chao-Qiang Lai; Jose M Ordovas; Robert J Straka; Hemant K Tiwari; Donna K Arnett
Journal:  Pharmacogenet Genomics       Date:  2012-10       Impact factor: 2.089

Review 2.  Pleiotropic effects of fibrates.

Authors:  Giulia Chinetti-Gbaguidi; Jean Charles Fruchart; Bart Staels
Journal:  Curr Atheroscler Rep       Date:  2005-09       Impact factor: 5.113

3.  The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study.

Authors:  A C Frazier-Wood; J M Ordovas; R J Straka; J E Hixson; I B Borecki; H K Tiwari; D K Arnett
Journal:  Pharmacogenomics J       Date:  2012-05-01       Impact factor: 3.550

4.  Strength Training for Arthritis Trial (START): design and rationale.

Authors:  Stephen P Messier; Shannon L Mihalko; Daniel P Beavers; Barbara J Nicklas; Paul DeVita; J Jeffery Carr; David J Hunter; Jeff D Williamson; Kim L Bennell; Ali Guermazi; Mary Lyles; Richard F Loeser
Journal:  BMC Musculoskelet Disord       Date:  2013-07-15       Impact factor: 2.362

5.  Short-term effect of fenofibrate on C-reactive protein: A meta-analysis of randomized controlled trials.

Authors:  Jiatao Ye; James N Kiage; Donna K Arnett; Alfred A Bartolucci; Edmond K Kabagambe
Journal:  Diabetol Metab Syndr       Date:  2011-09-22       Impact factor: 3.320

6.  Cerivastatin for lowering lipids.

Authors:  Stephen P Adams; Nicholas Tiellet; Nima Alaeiilkhchi; James M Wright
Journal:  Cochrane Database Syst Rev       Date:  2020-01-25

7.  Gene Expression Profiling of Markers of Inflammation, Angiogenesis, Coagulation and Fibrinolysis in Patients with Coronary Artery Disease with Very High Lipoprotein(a) Levels Treated with PCSK9 Inhibitors.

Authors:  Katja Hrovat; Andreja Rehberger Likozar; Janja Zupan; Miran Šebeštjen
Journal:  J Cardiovasc Dev Dis       Date:  2022-07-01

Review 8.  Effect of lipid-lowering and anti-hypertensive drugs on plasma homocysteine levels.

Authors:  Jutta Dierkes; Claus Luley; Sabine Westphal
Journal:  Vasc Health Risk Manag       Date:  2007
  8 in total

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