Heart failure & cardiomyopathies

Efficacy and Safety of Finerenone Across the Ejection Fraction Spectrum in Heart Failure With Mildly Reduced or Preserved Ejection Fraction: A Prespecified Analysis of the FINEARTS-HF Trial

CirculationPublished Prespecified secondary analysis of the FINEARTS-HF randomised trial

Authors' conclusion

In patients with HF with mildly reduced or preserved ejection fraction, finerenone reduced the risk of cardiovascular death and worsening HF events, irrespective of LVEF.

Study context

Population
Patients with heart failure (HF) and left ventricular ejection fraction (LVEF) ≥40% (mildly reduced or preserved EF)LVEF available for 5993
Participants
6,001 patients
Comparison
Finerenone vs placebo, by LVEF
Primary endpoint
Composite of:
  • Total (first and recurrent) worsening HF events
  • CV death
Methodological detailsplacebo-controlled, prespecified analysis by LVEF
  • Placebo-controlled
  • Prespecified analysis by LVEF

Primary result

As reported in the abstract

Finerenone vs PlaceboRate ratio (95% CI)
LVEF <50% (n = 2172)
0.84(0.68–1.03)
LVEF ≥50% to <60% (n = 2674)
0.80(0.66–0.97)
LVEF ≥60% (n = 1147)
0.94(0.70–1.25)
No modification of benefit across LVEF as a continuous variable
P for interaction = 0.28

Further findings

Total worsening HF events, by LVEF

Similar consistent effect of finerenone across LVEF
continuous Pinteraction=0.26

Baseline LVEF

Mean LVEF
53±8%
Median LVEF (IQR 46%-58%)
53%

Original publication

Efficacy and Safety of Finerenone Across the Ejection Fraction Spectrum in Heart Failure With Mildly Reduced or Preserved Ejection Fraction: A Prespecified Analysis of the FINEARTS-HF Trial. Circulation. Published 29 September 2024. doi:10.1161/circulationaha.124.072011

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