BPG is committed to discovery and dissemination of knowledge
Meta-Analysis
Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Cardiol. Apr 26, 2026; 18(4): 118879
Published online Apr 26, 2026. doi: 10.4330/wjc.v18.i4.118879
Clinical outcomes of finerenone in heart failure: A systematic review and meta-analysis
Maneeth Mylavarapu, Madiha Kiyani, Andrew Ndakotsu, Vaibhav Vats, Nithin Karnan, Elizabeth Caroline Palaparthi, Mahnoor Anjum, Lakshmi Sai Meghana Kodali, Aneeza Jamshed, Fabio Enrique Parada Cabrera
Maneeth Mylavarapu, Aneeza Jamshed, Department of Cardiology, Endeavor Health Cardiovascular Institute, Glenview, IL 60026, United States
Maneeth Mylavarapu, Aneeza Jamshed, Division of Cardiology, Department of Medicine, University of Chicago Pritzker School of Medicine, Chicago, IL 60637, United States
Madiha Kiyani, Andrew Ndakotsu, Department of Internal Medicine, MedStar Health, Georgetown University, Washington, District of Columbia 20007, United States
Vaibhav Vats, Department of Internal Medicine, Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, United States
Nithin Karnan, Department of Internal Medicine, MercyOne North Iowa Medical Center, Mason, IA 50401, United States
Elizabeth Caroline Palaparthi, Department of Internal Medicine, Prime Health Consortium-Shasta Regional Medical Center, Redding, CA 96001, United States
Mahnoor Anjum, Department of Medicine, Advent Health Tampa, Tampa, FL 33613, United States
Lakshmi Sai Meghana Kodali, Division of Preventive Cardiology, Department of Cardiology, Inova Schar Heart and Vascular, Inova Health System, Fairfax, VA 22031, United States
Fabio Enrique Parada Cabrera, Department of Cardiology, Instituto Guatemalteco de Seguridad Social, Guatemala 01001, Guatemala
Co-first authors: Maneeth Mylavarapu and Madiha Kiyani.
Author contributions: Mylavarapu M and Kiyani M has made significant contributions in terms of conceptualization, thus qualified as the co-first authors of the paper; Kodali LSM and Mylavarapu M performed data curation, visualization, and interpretation; Mylavarapu M, Kiyani M, Ndakotsu A, Vats V, Karnan N, Palaparthi EC, Anjum M, Kodali LSM, Jamshed A, and Cabrera FEP wrote, reviewed and edited the manuscript; and all authors have read and approved the final manuscript.
Conflict-of-interest statement: No conflicts of interests to disclose.
PRISMA 2009 Checklist statement: The authors have read the PRISMA 2009 Checklist, and the manuscript was prepared and revised according to the PRISMA 2009 Checklist.
Corresponding author: Maneeth Mylavarapu, MD, Senior Researcher, Department of Cardiology, Endeavor Health Cardiovascular Institute, 2100 Pfingsten Road, Glenview, IL 60026, United States. dr.maneeth.mylavarapu@gmail.com
Received: January 13, 2026
Revised: February 14, 2026
Accepted: March 19, 2026
Published online: April 26, 2026
Processing time: 91 Days and 8.4 Hours
Abstract
BACKGROUND

Chronic kidney disease (CKD) and heart failure (HF) frequently coexist, creating a complex clinical challenge. Mineralocorticoid receptor antagonists (MRAs) have shown promise in managing both conditions, primarily by mitigating the adverse effects of aldosterone. Finerenone, a novel nonsteroidal MRA, has demonstrated significant benefits in reducing cardiovascular and renal events in patients with CKD and type 2 diabetes. However, while the efficacy and safety of finerenone have been extensively evaluated in CKD populations, its effects in patients with HF, particularly those without concurrent significant CKD, require further investigation.

AIM

To investigate the efficacy and safety of finerenone in patients with HF.

METHODS

Per the PRISMA guidelines, a thorough search was conducted in PubMed/MEDLINE, Science Direct, and Google Scholar, and relevant randomized control trials (RCTs) comparing finerenone to placebo or other agents on clinical outcomes in patients with HF were included.

RESULTS

Four RCTs involving 7457 patients with HF (mean age, 71.85 years; females, 41.0%) were included in the study. Of them, 4160 received finerenone (mean age, 71.7 years) and 3297 received a placebo (mean age, 72.04 years). The finerenone group had significantly lower odds of worsening HF [odds ratio (OR) = 0.76; 95%CI: 0.66-0.88; P = 0.0001] and improvement in the Kansas City Cardiomyopathy Questionnaire (mean differences: 1.60; 95%CI: 1.58-1.62; P < 0.0001). Furthermore, higher odds of hyperkalemia (OR = 1.32; 95%CI: 0.58-2.99; P = 0.51) and lower odds of adverse event (AE) (OR = 0.91; 95%CI: 0.72-1.15; P = 0.44) and severe AE (OR = 0.99; 95%CI: 0.88-1.10; P = 0.82).

CONCLUSION

Our meta-analysis demonstrates that finerenone significantly reduces the risk of worsening of HF and improves quality of life in HF. However, finerenone was associated with increased risks of hyperkalemia, requiring clinical vigilance. Future research should focus on long-term outcomes and the optimal dosing of finerenone in specific HF subpopulations, including those receiving other guideline-directed medical therapies.

Keywords: Finerenone; Heart failure; Nonsteroidal mineralocorticoid receptor antagonists; Kansas City Cardiomyopathy Questionnaire; Hyperkalemia; Meta-analysis

Core Tip: Finerenone, a novel nonsteroidal mineralocorticoid receptor antagonist, has shown clear benefits in chronic kidney disease, but its specific impact on heart failure (HF) has required further synthesis. Our meta-analysis of 7457 patients reveals that finerenone significantly decreases the odds of worsening HF and enhances quality of life scores. However, potential safety signals, including hyperkalemia, suggest that while finerenone is a potent tool for managing HF, its use requires vigilant monitoring to balance clinical benefits against adverse events.