Why the study?
Patients with T2DM and CKD face high renal and cardiovascular risks, but the real-world safety and effectiveness of finerenone remain underexplored in local settings.
Does finerenone improve albuminuria, eGFR, and blood pressure in patients with type 2 diabetes mellitus and chronic kidney disease?
Does finerenone improve albuminuria, eGFR, and blood pressure in patients with type 2 diabetes mellitus and chronic kidney disease?
In a real-world Latin American cohort of patients with type 2 diabetes mellitus and chronic kidney disease, six months of finerenone therapy significantly reduced albuminuria and blood pressure with good tolerability and stable eGFR.
Supports real-world tolerability in Latin America; leaves open need for randomized outcome trials.
BACKGROUND: Patients with type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD) face high renal and cardiovascular risks. Finerenone, a selective non-steroidal mineralocorticoid receptor antagonist, has demonstrated efficacy in reducing these risks in clinical trials. However, its real-world safety and effectiveness remain underexplored in local settings. AIM: To evaluate the real-world safety and effectiveness of finerenone in patients with T2DM and CKD across seven Latin American countries. METHODS: We conducted an observational, multicenter, retrospective cohort study based on real-world data in 347 patients with T2DM and CKD [urinary albumin-creatinine ratio (UACR) > 30 mg/g]. Patients received finerenone (10 mg or 20 mg daily), and clinical and laboratory parameters were evaluated at baseline and after six months of treatment. RESULTS: (27.0-52.0). CONCLUSION: In our cohort of patients with CKD associated with T2DM, finerenone proved to be an effective short-term therapy for reducing albuminuria, demonstrating very good tolerance and a low risk of hyperkalemia.
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Arnedo et al. (2026) studied this question.
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