Abstract Objective. To retrospectively analyze the efficacy and safety of finerenone in patients with IgA nephropathy (IgAN) without diabetes. Methods. A retrospective analysis was conducted on patients with primary IgAN who received standard treatment between September 2023 and June 2025. The patients were divided into the finerenone and control groups based on whether finerenone was used. The primary outcomes were the renal complete response (CR) rate (0.5 g/d) and renal endpoint events (defined as a 30% reduction in eGFR), and the secondary outcomes were the degree of decrease in 24-hour urine protein quantification, changes in eGFR, and safety outcomes. Results. A total of 382 patients were included (191 in the finerenone group and 191 in the control group). Finerenone significantly increased the CR rate compared with the control group (HR = 2.58, 95%CI: 1.82–3.66, P 0.001) and reduced the renal endpoint event (HR = 0.30, 95%CI: 0.07–0.91, P = 0.036). Finerenone combined with SGLT2i has a higher renal remission rate (with SGLT2i: HR: 3.52, 95%CI: 2.32–5.35; without SGLT2i: HR: 1.54, 95%CI: 0.75–3.19, Pinteraction = 0.032). The serum potassium levels in both groups remained consistent. Conclusion. Finerenone is safe and effective in treating IgAN patients without diabetes, and finerenone combined with SGLT2i has a higher CR rate.
Wang et al. (Thu,) studied this question.