Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Sep;34(9):599-608.
doi: 10.1007/s40261-014-0215-0.

Efficacy and safety of pitavastatin versus simvastatin: a meta-analysis of randomized controlled trials

Affiliations
Review

Efficacy and safety of pitavastatin versus simvastatin: a meta-analysis of randomized controlled trials

Zhen Jiang et al. Clin Drug Investig. 2014 Sep.

Abstract

Background and objectives: Pitavastatin is the latest statin to be approved and has shown beneficial effects on plasma lipid profiles. The aim of the present meta-analysis was to assess both the efficacy and safety of pitavastatin versus simvastatin, one of the most commonly used statins.

Methods: A search of the MEDLINE, EMBASE, OVID and Cochrane Central Register of Controlled Trials (CENTRAL) databases was undertaken. Clinical trials evaluating the efficacy and safety of simvastatin versus pitavastatin, published up to February 2014, were identified. Trials were included if they (1) were randomized controlled trials (RCTs) of at least 12 weeks' duration; (2) included patients with primary hypercholesterolaemia or mixed dyslipidaemia; (3) studied outcomes included low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), triglyceride (TG) and high-density lipoprotein cholesterol (HDL-C); and (4) were published in the English language. A fixed-effects model was used for data analysis if no significant heterogeneity was present; otherwise a random-effects model was used. Efficacy is reflected by the mean difference in the percentage change of plasma lipid profiles. Treatment-emergent adverse events (TEAEs) are presented as risk ratio (RR).

Results: A total of 1,468 patients were included in the meta-analysis. The results indicated similar efficacy of pitavastatin (versus simvastatin) in lowering LDL-C. Pitavastatin also had similar effects to simvastatin on other major aspects of plasma lipids, including TC, TG and HDL-C. Somewhat in contrast to common belief (based on distinct metabolism by P450 subtypes), the two statins did not differ in the incidence of TEAE.

Conclusions: In clinical trials, pitavastatin was comparable to simvastatin in both efficacy and safety profile. Large-scale, high-quality observational studies are required to determine whether the advantage of pitavastatin in metabolism profiles could be translated into noticeable benefits.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Atheroscler Thromb. 2009 Oct;16(5):654-61 - PubMed
    1. Int J Cardiol. 2014;172(1):e199-200 - PubMed
    1. Expert Rev Cardiovasc Ther. 2013 Dec;11(12):1597-612 - PubMed
    1. J Clin Lipidol. 2008 Dec;2(6):453-63 - PubMed
    1. J Lipid Res. 2004 May;45(5):948-53 - PubMed

MeSH terms

LinkOut - more resources