Key result
Finerenone cuts worsening HF and CV death consistently across LVEF categories.
Why the study?
Does finerenone reduce the composite of total worsening HF events and cardiovascular death consistently across the ejection fraction spectrum in patients with heart failure and LVEF ≥40%?
RCT (n=6,001)
placebo-controlled
randomized
Does finerenone reduce the composite of total worsening HF events and cardiovascular death consistently across the ejection fraction spectrum in patients with heart failure and LVEF ≥40%?
Finerenone provides consistent cardiovascular benefits in patients with heart failure and LVEF ≥40%, irrespective of baseline ejection fraction.
Background: The effect of treatments for heart failure may vary among patients according to left ventricular ejection fraction (LVEF). In the FINEARTS-HF, the nonsteroidal MRA finerenone reduced the risk of cardiovascular death and total worsening heart failure events in patients with heart failure with mildly reduced or preserved ejection fraction (HFmrEF/HFpEF). We examined the effect of finerenone according to LVEF in FINEARTS-HF. Methods: FINEARTS-HF was a randomized, placebo-controlled trial examining the efficacy and safety of finerenone in patients with heart failure and LVEF �%. The treatment effect of finerenone was examined in prespecified analyses according to LVEF categories (<50%, ≥50 to <60%, and ≥60%) and with LVEF as a continuous variable. The primary outcome was a composite of total (first and recurrent) worsening HF events and cardiovascular death. Results: Baseline LVEF data were available for 5993 of the 6001 participants in FINEARTS-HF. Mean and median LVEF were 53 ± 8% and 53% (IQR 46% -58%), respectively. LVEF was <50% in 2172 (36), between 50 to <60% in 2674 (45%), and ≥60% in 1147 (19%). Patients with a higher LVEF were older, more commonly female, were less likely to have a history of coronary artery disease, and more frequently had a history of hypertension and chronic kidney disease compared to those with a lower LVEF. Finerenone reduced the risk of cardiovascular death and total heart failure events consistently across LVEF categories: LVEF <50% rate ratio (RR) = 0.84 (95% CI 0.68, 1.03), LVEF ≥50 to <60% RR = 0.80 (0.66, 0.97) and LVEF ≥60% RR = 0.94 (0.70, 1.25); p interaction = 0.70. There was no modification of the benefit of finerenone across the range of LVEF when analyzed as a continuous variable (p interaction = 0.28). There was a similar consistent effect of finerenone on reducing the total number of worsening heart failure events (continuous p interaction = 0.26). Conclusions: In patients with HFmrEF/HFpEF, finerenone reduced the risk of cardiovascular death and worsening heart failure events, irrespective of LVEF.
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Docherty et al. (2024) conducted an RCT in heart failure with mildly reduced or preserved ejection fraction (HFmrEF/HFpEF) (n=6,001). Finerenone vs. placebo was evaluated on composite of total (first and recurrent) worsening HF events and cardiovascular death. Finerenone reduced the risk of cardiovascular death and worsening heart failure events consistently across LVEF categories (LVEF <50% RR 0.84; 50-<60% RR 0.80; ≥60% RR 0.94; p interaction=0.70).
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