ArticleEuropean heart journal. Cardiovascular pharmacotherapy2025
Nonsteroidal mineralocorticoid receptor antagonists and cardiovascular events in type 2 diabetes: a retrospective study.
Article in European heart journal. Cardiovascular pharmacotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Cardiovascular events with esaxerenone versus spironolactone in hypertension.Journal of human hypertension · 2026Article
- Colchicine use after acute myocardial infarction is associated with reduced dialysis dependence in advanced chronic kidney disease.Scientific reports · 2026Article
- Association of glucagon-like peptide-1 receptor agonist use with clinical outcomes in patients with rheumatoid arthritis and type 2 diabetes.Journal of diabetes investigation · 2026Article
- Plasma aldosterone concentration and valvular heart disease in hypertensive patients: a large cross-sectional study.Scientific reports · 2026Article
- Real-world evidence of finerenone in Type 2 diabetes: addressing confounding and follow-up duration.European heart journal. Cardiovascular pharmacotherapy · 2026Article
- Finerenone for diabetic hearts: a critical appraisal of MACE benefits and the research road ahead.European heart journal. Cardiovascular pharmacotherapy · 2026Article
- Association between sodium-glucose cotransporter 2 inhibitor use and clinical outcomes in patients with type 2 diabetes after urinary tract infection.Diabetes, obesity & metabolism · 2025Article
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Authors and funding
5 authors.
Funding
Abstract
aimsNonsteroidal mineralocorticoid receptor antagonists such as finerenone mitigate cardiorenal risks in patients with type 2 diabetes mellitus (T2DM). Real-world evidence comparing finerenone with spironolactone and eplerenone remains limited. This study aimed to evaluate the cardiovascular outcomes in T2DM patients treated with finerenone vs. spironolactone or eplerenone using real-world data. METHODS AND
resultsA retrospective cohort analysis was conducted using the TriNetX US Collaborative Network database. Adult patients with T2DM who were newly prescribed finerenone, spironolactone, or eplerenone were included (2021-2024). One-to-one propensity score matching was applied to eligible participants, resulting in 2957 finerenone users matching with spironolactone users and 1603 finerenone users matching with eplerenone users. Cardiovascular outcomes, including major adverse cardiovascular events (MACEs), heart failure, and mortality, were assessed over 24 months of follow-up. Hazard ratios (HRs) with 95% confidence intervals (CI) were calculated using Cox regression models. Finerenone users had significantly lower rates of MACE compared with spironolactone users (HR: 0.53, 95% CI: 0.43-0.66) and eplerenone (HR: 0.66, 95% CI: 0.50-0.87). Mortality was also reduced with finerenone vs. spironolactone (HR: 0.45, 95% CI: 0.35-0.57) and eplerenone (HR: 0.56, 95% CI: 0.41-0.75). Heart failure events were fewer with finerenone than with spironolactone (HR: 0.70, 95% CI: 0.55-0.90) and eplerenone (HR: 0.70, 95% CI: 0.50-0.99). Differences in acute myocardial infarction and stroke rates were not statistically significant.
conclusionFinerenone demonstrated superior cardiovascular outcomes compared with spironolactone and eplerenone in patients with T2DM with significant reductions in MACE, mortality, and heart failure events.
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