Key result
Eplerenone reduces all-cause mortality ~22% vs. spironolactone in heart failure.
Why the study?
Both eplerenone and spironolactone improve prognosis in heart failure, but the difference in clinical effects between them remained uncertain.
Does eplerenone reduce all-cause mortality in patients with heart failure compared to spironolactone?
Meta-Analysis (n=21,930)
Yes
Does eplerenone reduce all-cause mortality in patients with heart failure compared to spironolactone?
Eplerenone is associated with significantly lower all-cause mortality, cardiovascular mortality, and fewer adverse events like gynecomastia compared to spironolactone in patients with heart failure.
Supports preferring eplerenone over spironolactone in heart failure; extends trial data with pooled mortality and safety benefits.
BACKGROUND: Eplerenone and spironolactone, recognized as mineralocorticoid receptor antagonists (MRAs), have been reported to improve clinical prognosis among individuals diagnosed with heart failure (HF). However, the difference in the clinical effects between eplerenone and spironolactone in individuals with HF remains uncertain. We aimed to assess the impact of eplerenone compared to spironolactone on clinical outcomes within the HF population. METHODS: An extensive search was executed in several databases (PubMed, Web of Science, Scopus, Cochrane Library). All relevant studies evaluating eplerenone compared to spironolactone in patients with HF were included. Dichotomous data were pooled as Hazard ratio (HR) or Risk ratio (RR) with a 95% confidence interval (CI). Our main outcome was all-cause mortality. Secondary outcomes included death from cardiovascular causes, treatment withdrawal, and gynecomastia. RESULTS: Ten studies, comprising 21,930 HF individuals, were included in our investigation. Eplerenone showed a lower risk of all-cause mortality (HR = 0.78, 95%CI [0.64 to 0.94], P = 0.009) and cardiovascular mortality (HR = 0.54, 95%CI [0.39, 0.74], P = 0.0001) compared to spironolactone. Furthermore, eplerenone exhibited a reduced risk of treatment withdrawal (RR = 0.69, 95% CI [0.62, 0.78], P = 0.0001) and gynecomastia (RR = 0.07, 95% CI [0.02 to 0.31], P = 0.0001) than spironolactone. CONCLUSION: Eplerenone revealed lower all-cause and cardiovascular mortality events in comparison to spironolactone. Moreover, eplerenone was associated with lower gynecomastia and treatment withdrawal events compared to spironolactone. Further well-designed randomized controlled trials are still warranted better to identify the clinical differences between eplerenone and spironolactone. TRIAL REGISTRATION: Protocol registration: https://doi.org/10.17605/OSF.IO/VNMGK.
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Elshahat et al. (2024) conducted a meta-analysis in Heart failure (n=21,930). Eplerenone vs. Spironolactone was evaluated on All-cause mortality (HR 0.78, 95% CI 0.64, 0.94, p=0.009). Eplerenone significantly reduced the risk of all-cause mortality by 22% (HR 0.78) compared to spironolactone in patients with heart failure.
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