Key result
Finerenone reduces CV death and worsening HF events ~16% vs placebo in HFmrEF and HFpEF.
Why the study?
The benefit of mineralocorticoid receptor blockade is less well established in heart failure with mildly reduced and preserved ejection fraction.
Does finerenone reduce cardiovascular death and worsening heart failure events in patients with HFmrEF or HFpEF?
Does finerenone reduce cardiovascular death and worsening heart failure events in patients with HFmrEF or HFpEF?
Effect estimate: RR 0.84 (95% CI 0.74-0.95)
p-value: p=0.007
Finerenone significantly reduces the composite of cardiovascular death and worsening heart failure in patients with HFmrEF or HFpEF, presenting a potential new pillar of therapy for this population.
May support finerenone in HFmrEF/HFpEF; leaves open practice change given low-certainty evidence.
Mineralcorticoid receptor (MR) blockade is a mainstay of treatment for heart failure with reduced ejection fraction (HFrEF); however, the benefit is less well established in heart failure with mildly reduced ejection fraction (HFmrEF) and preserved ejection fraction (HFpEF). The TOPCAT study failed to demonstrate a reduction in cardiovascular mortality and heart failure (HF) hospitalizations in this population but suggested potential benefits of mineralocorticoid receptor antagonists (MRAs) in specific patients subgroups. The FINEARTS-HF study, which evaluated the non-steroidal MRA finerenone in patients with HFmrEF or HFpEF, demonstrated a significant reduction in the primary composite endpoint of cardiovascular death and events related to worsening of heart failure (WHF), primarily driven by a decrease in total WHF events. Moreover, the FINEARTS-HF study demonstrated consistent efficacy across the entire left ventricular ejection fraction (LVEF) spectrum, regardless of sodium-glucose cotransporter 2 inhibitors use, sex, or age, with an early onset of benefit and a favourable safety and tolerability profile. Finerenone is currently indicated in class I in diabetic patients with chronic kidney disease to reduce the risk of HF; in light of the FINEARTS-HF results, it could become a new pillar of therapy for patients with HFpEF and HFmrEF.
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Tolone et al. (2025) conducted a review in Heart failure with mildly reduced ejection fraction (HFmrEF) and preserved ejection fraction (HFpEF) (n=6,014). Finerenone vs. Placebo was evaluated on Composite of cardiovascular death and HF events (first or recurrent event, hospitalization or urgent visit for HF) (RR 0.84, 95% CI 0.74-0.95, p=0.007). Finerenone reduced the composite of cardiovascular death and worsening heart failure events by 16% compared to placebo in patients with HFmrEF and HFpEF.
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