Heart failure & cardiomyopathiesSecondary analysis

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
  • placebo-controlled
  • prespecified analysis by left ventricular ejection fraction (LVEF)

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 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

Primary result

As reported in the abstract

CV death and total worsening HF events, by LVEF category
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

Summarised from the published abstract; every number is checked against it