Literature DB >> 27468651

Impact of statin therapy on plasma resistin and visfatin concentrations: A systematic review and meta-analysis of controlled clinical trials.

Amirhossein Sahebkar1, Paolo Giorgini2, Valeria Ludovici3, Claudio Pedone4, Gianna Ferretti5, Tiziana Bacchetti6, Davide Grassi3, Paolo Di Giosia3, Claudio Ferri3.   

Abstract

The beneficial effects of statin therapy in reducing cardiovascular morbidity and mortality is not merely explained by the lipid-modulating effects. Although adipokines levels have been associated with cardiometabolic disorders, a few studies have explored the effect of statin on resistin and visfatin. We aimed to evaluate the impact of statin therapy on levels of resistin and visfatin through a meta-analysis of published studies. A systematic literature search in Medline and SCOPUS databases was conducted up to January 2015 to identify controlled trials assessing changes in plasma concentrations of visfatin and resistin during treatment with statins. Quantitative data synthesis was performed using a random-effects model, with weighed mean difference (WMD) and 95% confidence interval (CI) as summary statistics. 12 eligible studies with 14 treatment arms were included. Overall, 844 participants were studied. No significant change in plasma resistin concentrations was observed following statin therapy (WMD: -0.11ng/mL, CI: -1.94,1.73, p=0.909). This effect was robust and not affected by statin type, treatment duration and LDL-cholesterol concentrations. With respect to visfatin concentrations, there was a marginally significant reduction following statin therapy (WMD: -2.40ng/mL, CI: -4.79,-0.002, p=0.050). However, this effect size was weak and sensitive to three of the trials included in the analysis. This meta-analysis did not suggest any effect of statin therapy on plasma resistin levels, while a slight reduction in visfatin levels was found. The effect of statins on visfatin levels may represent a novel pleiotropic characteristic of these drugs.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Adipokines; Pleiotropic effect; Resistin; Statin; Visfatin

Mesh:

Substances:

Year:  2016        PMID: 27468651     DOI: 10.1016/j.phrs.2016.07.031

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  4 in total

1.  Serum resistin is associated with impaired endothelial function and a higher rate of adverse cardiac events in patients with peripheral artery disease.

Authors:  Joel L Ramirez; Sukaynah A Khetani; Greg J Zahner; Kimberly A Spaulding; Melinda S Schaller; Warren J Gasper; Nancy K Hills; Anne L Schafer; S Marlene Grenon
Journal:  J Vasc Surg       Date:  2018-10-03       Impact factor: 4.268

2.  Serum resistin as an independent marker of aortic stiffness in patients with coronary artery disease.

Authors:  Ji-Hung Wang; Chung-Jen Lee; Chiu-Fen Yang; Yu-Chih Chen; Bang-Gee Hsu
Journal:  PLoS One       Date:  2017-08-14       Impact factor: 3.240

3.  High serum resistin levels are associated with peripheral artery disease in the hypertensive patients.

Authors:  Bang-Gee Hsu; Chung-Jen Lee; Chiu-Fen Yang; Yu-Chih Chen; Ji-Hung Wang
Journal:  BMC Cardiovasc Disord       Date:  2017-03-15       Impact factor: 2.298

Review 4.  Functional Implications of HMG-CoA Reductase Inhibition on Glucose Metabolism.

Authors:  Ki Hoon Han
Journal:  Korean Circ J       Date:  2018-11       Impact factor: 3.243

  4 in total

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