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
. 2008 Apr;31(4):153-8.
doi: 10.1002/clc.20324.

A comparison of the aldosterone-blocking agents eplerenone and spironolactone

Affiliations
Review

A comparison of the aldosterone-blocking agents eplerenone and spironolactone

Allan Struthers et al. Clin Cardiol. 2008 Apr.

Abstract

Improved understanding of the adverse pharmacological properties of aldosterone has prompted investigation of the clinical benefits of blocking aldosterone at the receptor level. This article reviews the pharmacology, clinical efficacy, and tolerability of the two available blocking agents, spironolactone and eplerenone. A Medline search identified clinical studies assessing spironolactone and eplerenone. Priority was given to large, well-controlled, clinical trials and comparative studies. Pharmacological differences between spironolactone and eplerenone include lower affinity of eplerenone for progesterone, androgen, and glucocorticoid receptors; more consistently demonstrated nongenomic properties for eplerenone; and the presence of long-acting metabolites for spironolactone. Both agents effectively treat hypertension and heart failure but comparisons are complicated by the deficiency of head-to-head trials and differences between patient populations. There are differences in the tolerability profiles; spironolactone is associated with dose-dependent sexual side effects. Both agents produce dose-dependent increases in potassium concentrations, although the effect with spironolactone appears to be greater when both agents are administered at recommended doses. Choice of a specific agent should be based on individual patient issues, such as the nature of heart failure and patient concerns about adverse events.

PubMed Disclaimer

Comment in

References

    1. Struthers AD: Aldosterone blockade in cardiovascular disease. Heart 2004; 90: 1229–1234. - PMC - PubMed
    1. de Gasparo M, Joss U, Ramjoue HP, Whitebread SE, Haenni H, et al.: Three new epoxy‐spirolactone derivatives: characterization in vivo and in vitro. J Pharmacol Exp Ther 1987; 240: 650–656. - PubMed
    1. Gardiner P, Schrode K, Quinlan D, Martin BK, Boreham DR, et al.: Spironolactone metabolism: steady‐state serum levels of the sulfur‐containing metabolites. J Clin Pharmacol 1989; 29: 342–347. - PubMed
    1. Inspra [Product Information]. Chicago, IL: GD Searle; 2003.
    1. Chai W, Garrelds IM, de Vries R, Batenburg WW, van Kats JP, et al.: Nongenomic effects of aldosterone in the human heart: interaction with angiotensin II. Hypertension 2005; 46: 701–706. - PubMed

MeSH terms