Finerenone improves cardiorenal outcomes in patients with chronic kidney disease and type 2 diabetes, regardless of baseline HbA(1c) levels or insulin use.
OBJECTIVEFinerenone significantly improved cardiorenal outcomes in patients with chronic kidney disease (CKD) and type 2 diabetes (T2D) in the Finerenone in Reducing Kidney Failure and Disease Progression in Diabetic Kidney Disease trial. We explored whether baseline HbA(1c) level and insulin treatment influenced outcomes. RESEARCH DESIGN AND METHODSPatients with T2D, urine albumin-to-creatinine ratio (UACR) of 30-5,000 mg/g, estimated glomerular filtration rate (eGFR) of 25 to <75 mL/min/1.73 m(2), and treated with optimized renin-angiotensin system blockade were randomly assigned to receive finerenone or placebo. Efficacy outcomes included kidney (kidney failure, sustained decrease >= 40% in eGFR from baseline, or renal death) and cardiovascular (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure) composite endpoints. Patients were analyzed by baseline insulin use and by baseline HbA(1c) <7.5% (58 mmol/mol) or >= 7.5%. RESULTSOf 5,674 patients, 3,637 (64.1%) received insulin at baseline. Overall, 5,663 patients were included in the analysis for HbA(1c); 2,794 (49.3%) had baseline HbA(1c) <7.5% (58 mmol/mol). Finerenone significantly reduced risk of the kidney composite outcome independent of baseline HbA(1c) level and insulin use (P-interaction = 0.41 and 0.56, respectively). Cardiovascular composite outcome incidence was reduced with finerenone irrespective of baseline HbA(1c) level and insulin use (P-interaction = 0.70 and 0.33, respectively). Although baseline HbA(1c) level did not affect kidney event risk, cardiovascular risk increased with higher HbA(1c) level. UACR reduction was consistent across subgroups. Adverse events were similar between groups regardless of baseline HbA(1c) level and insulin use; few finerenone-treated patients discontinued treatment because of hyperkalemia. CONCLUSIONSFinerenone reduces kidney and cardiovascular outcome risk in patients with CKD and T2D, and risks appear consistent irrespective of HbA(1c) levels or insulin use.
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