Journal
JOURNAL OF HYPERTENSION
Volume 29, Issue 5, Pages 980-990Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/HJH.0b013e3283455ca5
Keywords
aldosteronism; eplerenone; hypertension; spironolactone; treatment
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Funding
- Pharmacia (now Pfizer Inc)
- National Institute for Health Research [NF-SI-0509-10222] Funding Source: researchfish
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Background Eplerenone is claimed to be a more selective blocker of the mineralocorticoid receptor than spironolactone being associated with fewer antiandrogenic side-effects. We compared the efficacy, safety and tolerability of eplerenone versus spironolactone in patients with hypertension associated with primary aldosteronism. Methods The study was multicentre, randomized, double-blind, active-controlled, and parallel group design. Following a single-blind, placebo run-in period, patients were randomized 1 : 1 to a 16-week double-blind, treatment period of spironolactone (75-225 mg once daily) or eplerenone (100-300 mg once daily) using a titration-to-effect design. To be randomized, patients had to meet biochemical criteria for primary aldosteronism and have a seated DBP at least 90 mmHg and less than 120 mmHg and SBP less than 200 mmHg. The primary efficacy endpoint was the antihypertensive effect of eplerenone versus spironolactone to establish noninferiority of eplerenone in the mean change from baseline in seated DBP. Results Changes from baseline in DBP were less on eplerenone (-5.6 +/- 1.3SE mmHg) than spironolactone (-12.5 +/- 1.3SE mmHg) [difference, -6.9 mmHg (-10.6, -3.3); P<0.001]. Although there were no significant differences between eplerenone and spironolactone in the overall incidence of adverse events, more patients randomized to spironolactone developed male gynaecomastia (21.2 versus 4.5%; P=0.033) and female mastodynia (21.1 versus 0.0%; P=0.026). Conclusion The antihypertensive effect of spironolactone was significantly greater than that of eplerenone in hypertension associated with primary aldosteronism. J Hypertens 29: 980-990 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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