Nonsteroidal MRAs were associated with a lower risk of 1-year all-cause mortality, hospitalization, and worsening heart failure compared with steroidal MRAs (HR 0.79; 95% CI 0.70-0.90; P<0.001).
Cohort (n=3,238)
Yes
Do nonsteroidal MRAs improve 1-year clinical outcomes compared to steroidal MRAs in adult patients with heart failure?
In a real-world propensity-matched cohort of heart failure patients, initiation of nonsteroidal MRAs was associated with a significantly lower 1-year risk of mortality, hospitalization, and worsening heart failure compared to steroidal MRAs.
Effect estimate: HR 0.79 (95% CI 0.70-0.90)
p-value: p=<0.001
Background Mineralocorticoid receptor antagonists (MRAs) reduce mortality and hospitalization in patients with heart failure (HF). Finerenone, a selective nonsteroidal MRA, has recently demonstrated clinical benefits in patients with HF. However, real‐world evidence comparing nonsteroidal and steroidal MRAs in HF is lacking. Methods We conducted a retrospective, propensity score–matched cohort study using the TriNetX database. Adult patients diagnosed with HF from January 2021 to February 2025 who initiated nonsteroidal or a steroidal MRA were included. The primary outcome was a composite of all‐cause mortality, all‐cause hospitalization, and worsening HF at 1 year. Secondary outcomes included each component individually and safety events. Subgroup and sensitivity analyses were performed, including Kaplan–Meier survival, E‐value estimation, and landmark analysis. Results After matching, 1619 patients were included in each group. The incidence of the primary composite outcome was significantly lower in the nonsteroidal MRAs group (hazard ratio HR, 0.79 95% CI, 0.70–0.90; P <0.001). Nonsteroidal MRAs were also associated with lower risks of all‐cause mortality (HR, 0.49), hospitalization (HR, 0.80), and worsening HF (HR, 0.76). Subgroup analyses showed consistent benefit. No significant differences in safety outcomes were observed. Conclusions In this large real‐world cohort, nonsteroidal MRAs use was associated with improved 1‐year clinical outcomes compared with steroidal MRAs in patients with HF. These findings support the potential clinical utility of nonsteroidal MRAs across HF phenotypes and highlight the need for further randomized studies to validate these results.
Wu et al. (Thu,) conducted a cohort in Heart failure (n=3,238). Nonsteroidal MRAs vs. Steroidal MRAs was evaluated on Composite of all-cause mortality, all-cause hospitalization, and worsening HF at 1 year (HR 0.79, 95% CI 0.70-0.90, p=<0.001). Nonsteroidal MRAs were associated with a lower risk of 1-year all-cause mortality, hospitalization, and worsening heart failure compared with steroidal MRAs (HR 0.79; 95% CI 0.70-0.90; P<0.001).
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