Mineralocorticoid Receptor Antagonists in Patients With Heart Failure and Impaired Renal Function

Background Kidney dysfunction often leads to reluctance to start or continue life-saving heart failure (HF) therapy. Objectives This study sought to examine the efficacy and safety of mineralocorticoid receptor antagonists (MRAs) in patients with HF with reduced ejection fraction experiencing significant kidney dysfunction. Methods We pooled individual patient data from the RALES (Randomized Aldactone Evaluation Study) and EMPHASIS-HF (Eplerenone in Mild Patients Hospitalization and Survival Study in Heart Failure) trials. The association between MRA treatment and outcomes was assessed according to whether the estimated glomerular filtration rate (eGFR) declined to <30 mL/min/1.73 m(2) or not. The primary outcome was cardiovascular death or HF hospitalization. Results Among 4,355 patients included, 295 (6.8%) experienced a deterioration of eGFR after randomization to <30 mL/min/1.73 m(2). These patients had more impaired baseline cardiac and kidney function (eGFR 47.3 +/- 13.4 mL/min/1.73 m(2) vs 70.5 +/- 21.8 mL/min/1.73 m(2)) and had a higher risk of the primary outcome than patients without eGFR deterioration (HR: 2.49; 95% CI: 2.01-3.08; P < 0.001). However, the risk reduction in the primary outcome with MRA therapy was similar in those who experienced a decrease in eGFR to <30 mL/min/1.73 m(2) (HR: 0.65; 95% CI: 0.43-0.99) compared with those who did not (HR: 0.63; 95% CI: 0.56-0.71) (P-interaction = 0.87). In patients with a decrease in eGFR to <30 mL/min/1.73 m(2), 21 fewer individuals (per 100 person-years) experienced the primary outcome with MRA treatment, vs placebo, compared with an excess of 3 more patients with severe hyperkalemia (>6.0 mmol/L). Conclusions Because patients experiencing a decrease in eGFR to <30 mL/min/1.73 m(2) are at very high risk, the absolute risk reduction with an MRA in these patients is large and this decline in eGFR should not automatically lead to treatment discontinuation. (c) 2024 by the American College of Cardiology Foundation.