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Impact of fibrate therapy on plasma plasminogen activator inhibitor-1: A systematic review and meta-analysis of randomized controlled trials.

Authors :
Sahebkar, Amirhossein
Simental-Mendía, Luis E.
Watts, Gerald F.
Golledge, Jonathan
Source :
Atherosclerosis (00219150). May2015, Vol. 240 Issue 1, p284-296. 13p.
Publication Year :
2015

Abstract

Objective The aim of this systematic review was to perform a meta-analysis of randomized controlled trials (RCTs) examining the efficacy of fibrate therapy in reducing plasma concentration or activity of plasminogen activator inhibitor 1 (PAI-1). Methods Scopus and MEDLINE databases were searched (up to October 15, 2014) to identify RCTs investigating whether fibrates lower plasma PAI-1 concentration or activity. A random-effects model and the generic inverse variance method were used for quantitative data synthesis. Sensitivity analyses were conducted using the one-study remove approach. Random-effects meta-regression was performed to assess the impact of potential moderators on the estimated effect sizes. Results A total of 14 RCTs examining the effects of gemfibrozil (6 trials), bezafibrate (4 trials), and fenofibrate (5 trials) were included. Meta-analysis suggested that fibrate therapy did not significantly reduce plasma PAI-1 concentration (weighed mean difference [WMD]: −11.39 ng/mL, 95% CI: −26.64, 3.85, p = 0.143) or activity (WMD: 2.02 U/mL, 95% CI: −0.87, 4.90, p = 0.170). These results remained unchanged after subgroup analysis according to duration of treatment (<12 and ≥12 weeks) and type of fibrate administered (fenofibrate, bezafibrate or gemfibrozil). The estimated effects of fibrate therapy on plasma concentration and activity of PAI-1 were independent of treatment duration and changes in plasma triglyceride levels in the meta-regression analysis. Conclusion This meta-analysis of RCTs suggested that fibrate therapy does not reduce plasma concentration or activity of PAI-I. The putative benefits of fibrate therapy in patients with cardiovascular disease appear to be exerted via mechanisms independent of effects on PAI-1. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219150
Volume :
240
Issue :
1
Database :
Academic Search Index
Journal :
Atherosclerosis (00219150)
Publication Type :
Academic Journal
Accession number :
102072761
Full Text :
https://doi.org/10.1016/j.atherosclerosis.2015.03.016