Key result
Finerenone is linked to stabilizing eGFR at ~0.5 ml/min/year, attenuated by MAFLD or elevated aldosterone.
Why the study?
Diabetes and obesity can induce excessive mineralocorticoid receptor activation, leading to nephropathy and cardiovascular disease progression, but finerenone's effects on eGFR decline and its association with MAFLD required investigation.
Does finerenone improve the annual rate of decline in eGFR in patients with type 2 diabetes and chronic kidney disease?
Cohort (n=35)
Does finerenone improve the annual rate of decline in eGFR in patients with type 2 diabetes and chronic kidney disease?
Absolute Event Rate: 0.5% vs -4.35%
p-value: p=<0.001
Finerenone improves the annual eGFR decline in patients with T2D and CKD, though concurrent MAFLD or elevated plasma aldosterone may attenuate this renoprotective effect.
Finerenone was associated with improved eGFR slope in T2D-CKD; hypothesis-generating for MAFLD or aldosterone attenuation pending randomized trials.
Introduction and Objective: Diabetes and obesity can induce excessive mineralocorticoid receptor (MR) activation, leading to the progression of nephropathy and cardiovascular disease. In this study, we investigated the effects of finerenone on the annual rate of decline in eGFR and its association with metabolic dysfunction-associated steatotic liver disease (MAFLD). We examined the relationship between changes in plasma aldosterone levels after finerenone administration and improvement in eGFR. Methods: The study included patients with type 2 diabetes who had albuminuria, an eGFR ≥30 mL/min/1.73 m², had been treated with finerenone for one year. Renal function was assessed using the annual eGFR decline before and after finerenone treatment. In study 1, the annual eGFR decline were compared between patients with and without MAFLD. In study 2, plasma aldosterone concentration (PAC) were measured before and after finerenone treatment. These parameters were compared between patients who showed improvement in the annual eGFR decline and those who did not. Results: In study 1, 35 patients were analyzed. The annual eGFR decline improved significantly from −4.35 ± 7.57 to 0.50 ± 6.69 ml/min/1.73 m²/year after finerenone administration (p < 0.001). Among the 27 patients with improved eGFR decline, 18.5% had MAFLD, whereas 55.5% of the 9 patients with unchanged or worsened eGFR decline had MAFLD, a significantly higher proportion (p < 0.01).In study 2, 21 patients were analyzed. PAC increased significantly after finerenone treatment. PAC levels were significantly lower in the eGFR improvement group (14 patients; 32.8 ± 37.4 pg/ml) compared with the non-improvement group (7 patients; 71.4 ± 49.0 pg/ml; p < 0.05). Conclusion: In patients with type 2 diabetes complicated by CKD and albuminuria, finerenone improved the annual eGFR decline, suggesting a potential renoprotective effect. However, the presence of MAFLD or elevated plasma aldosterone levels may attenuate the renoprotective effects of finerenone. Disclosure M. Higa: None. T. Ichijo: None.
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HIGA et al. (2026) conducted a cohort in Type 2 diabetes with chronic kidney disease and albuminuria (n=35). Finerenone vs. Pre-treatment baseline was evaluated on Annual eGFR decline (p=<0.001). Finerenone significantly improved the annual eGFR decline from -4.35 to 0.50 ml/min/1.73 m²/year (p<0.001), though this effect was attenuated by MAFLD or elevated aldosterone.
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