Key result
Finerenone linked to a ~5.5 mL/min/1.73 m²/year improvement in eGFR slope in DKD.
Why the study?
Real-world evidence regarding the association between finerenone maintenance doses (10 mg vs. 20 mg) and eGFR slope changes in patients with diabetic kidney disease remains scarce.
Does finerenone improve eGFR slope in patients with diabetic kidney disease?
Observational (n=104)
No
Does finerenone improve eGFR slope in patients with diabetic kidney disease?
Finerenone significantly attenuated eGFR decline in real-world patients with diabetic kidney disease, with the greatest slope improvement observed in patients maintained on a 10 mg/day dose and those with concomitant SGLT2 inhibitor use.
Finerenone was associated with improved eGFR trajectories in real-world diabetic kidney disease; extends trial evidence but leaves open dose and SGLT2i interactions for confirmation.
BackgroundFinerenone demonstrates renoprotective effects in clinical trials; however, real-world evidence regarding the association between maintenance doses (10 mg vs. 20 mg) and estimated glomerular filtration rate (eGFR) slope changes remains scarce.We investigated the real-world impact of finerenone dosage and baseline clinical factors on eGFR slope trajectory in patients with diabetic kidney disease (DKD). MethodsWe retrospectively analyzed 104 patients with DKD who initiated finerenone and completed at least six months of follow-up.The primary outcome was the change in annual eGFR slope from the one-year preinitiation period to the six-month post-initiation period.Secondary outcomes included changes in urinary albumin-to-creatinine ratio (UACR), urinary protein-to-creatinine ratio (UPCR), serum potassium, and blood pressure.Multivariable linear regression analysis was conducted to identify independent baseline factors associated with eGFR slope improvement. ResultsFollowing finerenone initiation, the overall eGFR slope improved from -5.20 to +0.27 mL/min/1.73m²/year (p = 0.0144).Among subgroup analyses, significant slope improvement was observed in patients maintained on the 10 mg/day dose (n = 52, from -7.11 to +3.35 mL/min/1.73m²/year, p = 0.00041), whereas the 20 mg/day group (n = 52) remained in a stable trajectory (-3.29 to -2.85 mL/min/1.73m²/year, p = 0.865).In multivariable analysis, concomitant sodium-glucose cotransporter 2 (SGLT2) inhibitor use (B = +9.79,p = 0.016), younger age, lower baseline eGFR, and lower body mass index were independently associated with slope improvement.UACR decreased significantly (p = 0.0098), while serum potassium increased modestly (+0.086 mmol/L, p = 0.045) without clinically meaningful blood pressure changes. ConclusionsFinerenone significantly attenuated eGFR decline in real-world patients with DKD, with slope improvement observed in patients maintained on the 10 mg/day dose.Concomitant SGLT2 inhibitor use was independently associated with greater improvement in eGFR slope, supporting the clinical utility and practical dose management of finerenone in routine practice.
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Otani et al. (2026) conducted an observational in Diabetic Kidney Disease (n=104). Finerenone vs. Pre-initiation period was evaluated on Change in annual eGFR slope (p=0.0144). Finerenone significantly attenuated eGFR decline in patients with diabetic kidney disease, improving the mean eGFR slope from -5.20 to +0.27 mL/min/1.73 m²/year.
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