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Review
. 2025 Sep 9;14(18):6355.
doi: 10.3390/jcm14186355.

Finerenone Versus Placebo on Renal Outcomes in Patients with Chronic Kidney Disease and Type 2 Diabetes: A Systematic Review and Meta-Analysis

Affiliations
Review

Finerenone Versus Placebo on Renal Outcomes in Patients with Chronic Kidney Disease and Type 2 Diabetes: A Systematic Review and Meta-Analysis

Gerson E Diaz et al. J Clin Med. .

Abstract

Background/Objectives: To evaluate the efficacy and safety of finerenone compared to placebo in improving renal outcomes in patients with chronic kidney disease (CKD) and type 2 diabetes (T2D). Methods: A systematic review and meta-analysis were conducted, compiling RCTs evaluated the effect of finerenone compared to placebo in patients with CKD and T2D. Inclusion criteria included adults with CKD and T2D. Outcomes included kidney failure, end-stage renal disease (ESKD), and persistently decreased glomerular filtration rate (eGFR). Secondary outcomes included cardiovascular events, hospitalization due to hyperkalemia, and serious adverse events. Pooled relative risks (RRs) and mean differences (MDs) were calculated using a random-effects model. Results: Three RCTs with a total of 19,027 patients were included. Finerenone demonstrated a potential reduction in kidney failure risk (RR 0.86, 95% CI: 0.35-2.13) and ESKD (RR 0.82, 95% CI: 0.54-1.23); however, confidence intervals included the null effect. There were no statistically significant differences, as seen in the decrease in eGFR (RR 1.03; 95% CI: 0.27-3.85), but also in mortality due to renal causes (RR 0.62; 95% CI: 0.00-7168.81). Finerenone increased hyperkalemia-related hospitalizations (RR 4.57, 95% CI: 1.07-19.48) but had no significant effect on serious adverse events (RR 0.94, 95% CI: 0.92-0.97) or systolic BP (MD 0.08 mmHg, 95% CI: -0.36 to 0.52). Conclusions: Finerenone may provide renal protection in CKD and T2D, though benefits remain uncertain due to wide confidence intervals and study heterogeneity. The increased risk of hyperkalemia warrants careful patient selection and monitoring. Further research is needed to refine its clinical applicability. Review registration: PROSPERO CRD420250642593.

Keywords: cardiovascular outcomes; chronic kidney disease; finerenone; meta-analysis; type 2 diabetes.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Figure 1
Figure 1
Flow chart selection process.
Figure 2
Figure 2
Effect of Finererone on kidney failure. Data from Bakris et al., 2020 [14], and Pitt et al., 2021 [12].
Figure 3
Figure 3
Effect of Finererone on end-stage kidney disease. Data from Bakris et al., 2020 [14], McCausland et al., 2024 [13], and Pitt et al., 2021 [12].
Figure 4
Figure 4
Effect of Finererone on Sustained decrease in eGFR. Data from Bakris et al., 2020 [14], McCausland et al., 2024 [13], and Pitt et al., 2021 [12].
Figure 5
Figure 5
Effect of Finererone on Sustained decrease of 40 in eGFR. Data from Bakris et al., 2020 [14], McCausland et al., 2024 [13], and Pitt et al., 2021 [12].
Figure 6
Figure 6
Effect of Finererone on Death from renal causes. Data from Bakris et al., 2020 [14], and Pitt et al., 2021 [12].
Figure 7
Figure 7
Effect of Finererone on Hospitalization due to hyperkalemia. Data from Bakris et al., 2020 [14], McCausland et al., 2024 [13], and Pitt et al., 2021 [12].
Figure 8
Figure 8
Effect of Finererone on any serious adverse event. Data from Bakris et al., 2020 [14], McCausland et al., 2024 [13], and Pitt et al., 2021 [12].
Figure 9
Figure 9
Effect of Finererone on SBP by eGFR at stage. Data from Bakris et al., 2020 [14], McCausland et al., 2024 [13], and Pitt et al., 2021 [12].

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