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DOI 10.1016/j.jchf.2025.03.041

Медицинская библиотека · JACC. Heart failure · 2025

Efficacy and Safety of Finerenone in Heart Failure With Preserved Ejection Fraction: A FINE-HEART Analysis.

Ostrominski John W, Filippatos Gerasimos, Claggett Brian L, Miao Zi Michael, Desai Akshay S, Jhund Pardeep S, D Henderson Alasdair, Scheerer Markus F, Rohwedder Katja, Amarante Flaviana, Brinker Meike, Lay-Flurrie James, Lam Carolyn S P, Senni Michele, Shah Sanjiv J, Voors Adriaan A, Zannad Faiez, Rossing Peter, Ruilope Luis M, Anker Stefan D, Pitt Bertram, Agarwal Rajiv, McMurray John J V, Solomon Scott D, Vaduganathan Muthiah

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

BACKGROUND

Pooling data from participants with heart failure with mildly reduced ejection fraction (HFmrEF) or heart failure with preserved ejection fraction (HFpEF) from all completed outcomes trials evaluating finerenone to date may enhance understanding of its safety and efficacy in this high-risk and heterogeneous population.

OBJECTIVES

In this prespecified participant-level pooled analysis of the FIDELIO-DKD, FIGARO-DKD, and FINEARTS-HF trials (FINE-HEART), we evaluated the safety and efficacy of finerenone in individuals with HFmrEF/HFpEF.

METHODS

The treatment effects of finerenone vs placebo on cardiovascular death or heart failure hospitalization were evaluated using Cox proportional hazards regression models stratified by trial. Additional endpoints included cardiovascular death, HF hospitalization, new-onset atrial fibrillation, and all-cause death.

RESULTS

Among 18,991 pooled trial participants, 7,008 (36.9%) had HFmrEF/HFpEF (mean age, 71 ± 10 years; 44% female). Over a median follow-up of 2.5 years, finerenone reduced cardiovascular death or heart failure hospitalization compared with placebo (HR: 0.87 [95% CI: 0.78-0.96]; P = 0.008). Consistent effects were observed across trials (Pinteraction = 0.24), key subgroups, and baseline estimated glomerular filtration rate (Pinteraction = 0.47), urine albumin-to-creatinine ratio (Pinteraction = 0.62), and glycated hemoglobin (Pinteraction = 0.93). Finerenone additionally appeared to reduce heart failure hospitalization (HR: 0.84 [95% CI: 0.74-0.94]; P = 0.003) and new-onset atrial fibrillation (HR: 0.75 [95% CI: 0.58-0.97]; P = 0.030), but did not statistically significantly decrease cardiovascular death or all-cause death. Hyperkalemia was more common, and hypokalemia was less common, with finerenone vs placebo. Serious adverse events were similar between the treatment arms.

CONCLUSIONS

This participant-level pooled analysis of 3 large-scale outcomes trials supports the use of finerenone in individuals with HFmrEF/HFpEF across a broad range of cardiovascular-kidney-metabolic risk. (FINE-HEART: An Integrated Pooled Analysis of Finerenone across 3 Phase III Trials of Heart Failure and Chronic Kidney Disease and Type 2 Diabetes; CRD42024570467).

Для цитирования: Ostrominski John W, Filippatos Gerasimos, Claggett Brian L, Miao Zi Michael, Desai Akshay S, Jhund Pardeep S, D Henderson Alasdair, Scheerer Markus F, Rohwedder Katja, Amarante Flaviana, Brinker Meike, Lay-Flurrie James, Lam Carolyn S P, Senni Michele, Shah Sanjiv J, Voors Adriaan A, Zannad Faiez, Rossing Peter, Ruilope Luis M, Anker Stefan D, Pitt Bertram, Agarwal Rajiv, McMurray John J V, Solomon Scott D, Vaduganathan Muthiah. Efficacy and Safety of Finerenone in Heart Failure With Preserved Ejection Fraction: A FINE-HEART Analysis.. JACC. Heart failure. 2025. DOI: 10.1016/j.jchf.2025.03.041.

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