Abstract 4369294: Estimated Lifetime Benefits of Finerenone on Cardiorenal Morbidity and Mortality in Patients with Type 2 Diabetes and Chronic Kidney Disease
Introduction: Finerenone, a non-steroidal mineralocorticoid receptor antagonist, improves cardiovascular and kidney outcomes in people with type 2 diabetes and chronic kidney disease (CKD). However, the long-term impact of finerenone on delaying or preventing cardiorenal events is not known. Purpose: To estimate the lifetime benefits of finerenone vs. placebo on cardiorenal morbidity and mortality in persons with type 2 diabetes and CKD. Methods: In this participant-level pooled analysis of the FIDELIO-DKD and FIGARO-DKD trials (FIDELITY), we estimated the effects of finerenone on long-term survival free from cardiorenal morbidity and mortality using validated, nonparametric, and age-based actuarial methods. The main outcome was a cardiorenal composite outcome comprised of all-cause death and the individual components of the prespecified cardiovascular (heart failure hospitalization, non-fatal myocardial infarction, or non-fatal stroke) and kidney (CKD progression [sustained ≥57% decrease in eGFR] or kidney failure) composite endpoints. Results: Among 12,990 pooled trial participants, the risk of cardiorenal morbidity or mortality was lower with finerenone (71.8 events per 1000 person-years) vs. placebo (85.4 events per 1000 patient years; HR, 0.84 [95% CI, 0.78 to 0.90]) over a median trial follow-up of 3.0 [2.3, 3.8] years. In actuarial analyses examining lifetime trajectories for a 65-year-old trial participant, mean survival free from cardiorenal morbidity or mortality was 10.2 years (95% CI, 9.7 to 10.7) with placebo and 11.5 years (95% CI, 11.0 to 12.0) with finerenone, representing an additional 1.3 years (95% CI, 0.6 to 2.0 years) of event-free survival ( Figure, Panel A ). Cardiorenal event-free survival gains were observed across a broad age range, from 1.2 years (95% CI, 0.2 to 2.3 years) at age 55 to 0.8 years (95% CI, 0.1 to 1.4 years) at age 75 ( Figure, Panel B ). Conclusions: Treatment with finerenone is projected to afford clinically relevant long-term gains in survival free from cardiorenal morbidity and mortality, reinforcing its role as a key component of guideline-directed medical therapy for persons with type 2 diabetes and CKD.
Authors
- Stefan D. Anker (ORCID: https://orcid.org/0000-0002-0805-8683)
- Brendon Lange Neuen (ORCID: https://orcid.org/0000-0001-9276-8380)
- John W. Ostrominski (ORCID: https://orcid.org/0000-0002-2866-9414)
- John J.V. McMurray (ORCID: https://orcid.org/0000-0002-6317-3975)
- Katja Rohwedder
- Luís M. Ruilope (ORCID: https://orcid.org/0000-0001-6278-7951)
- Patrick Schloemer (ORCID: https://orcid.org/0009-0004-7787-5662)
- Brian Claggett
- Meike Brinker (ORCID: https://orcid.org/0000-0002-1560-9535)
- Muthiah Vaduganathan (ORCID: https://orcid.org/0000-0003-0885-1953)
- Andrea Lage
- Peter R Rossing (ORCID: https://orcid.org/0000-0002-1531-4294)
- Rajiv Agarwal (ORCID: https://orcid.org/0000-0001-8355-7100)
- Scott D Solomon
Institutions
- Brigham and Women's Hospital (US)
- Steno Diabetes Centers (DK)
- Indianapolis Zoo (US)
- British Heart Foundation (GB)
- Research Institute Hospital 12 de Octubre (ES)
- The George Institute for Global Health (AU)
- Bayer (Germany) (DE)
- Charité - Universitätsmedizin Berlin (DE)
Publication Details
- Journal
- Circulation
- Published
- 2025-11-03
- DOI
- https://doi.org/10.1161/circ.152.suppl_3.4369294
- Primary Topic
- Hormonal Regulation and Hypertension
- Type
- article
- Field-Weighted Citation Impact
- 0.00