Finerenone and Heart Failure Outcomes by Kidney Function/Albuminuria in Chronic Kidney Disease and Diabetes

dc.contributor.authorFilippatos, Gerasimos
dc.contributor.authorAnker, Stefan D.
dc.contributor.authorPitt, Bertram
dc.contributor.authorRossing, Peter
dc.contributor.authorJoseph, Amer
dc.contributor.authorKolkhof, Peter
dc.contributor.authorLambelet, Marc
dc.contributor.authorLawatscheck, Robert
dc.contributor.authorBakris, George L.
dc.contributor.authorRuilope, Luis M.
dc.contributor.authorAgarwal, Rajiv
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-06-06T14:51:22Z
dc.date.available2024-06-06T14:51:22Z
dc.date.issued2022
dc.description.abstractBackground: In patients with type 2 diabetes (T2D), risks of cardiovascular mortality and heart failure (HF) increase with decreasing kidney function (estimated glomerular filtration rate [eGFR]) and increasing albuminuria (urine albumin-to-creatinine ratio [UACR]). Finerenone, a selective, nonsteroidal mineralocorticoid receptor antagonist, improved cardiorenal outcomes in patients with chronic kidney disease (CKD) and T2D in FIDELITY (Finerenone in Chronic Kidney Disease and Type 2 Diabetes: Combined FIDELIO-DKD and FIGARO-DKD Trial Programme Analysis). Objectives: This study sought to evaluate the effects of finerenone on HF outcomes by eGFR and/or UACR categories. Methods: FIDELITY included 13,026 patients with T2D and CKD (UACR 30-5,000 mg/g and eGFR ≥25 mL/min/1.73 m2) randomized to finerenone or placebo. Time-to-event outcomes were first hospitalization for heart failure (HHF), cardiovascular death or first HHF, recurrent HHF, and cardiovascular death or recurrent HHF, analyzed in subgroups by baseline eGFR (<60 and ≥60 mL/min/1.73 m2) and/or UACR (<300 and ≥300 mg/g). Results: Compared with placebo, finerenone significantly reduced risk of first HHF (HR: 0.78 [95% CI: 0.66-0.92]; P = 0.003), cardiovascular death or first HHF (HR: 0.83 [95% CI: 0.74-0.93]; P = 0.002), recurrent HHF (HR: 0.79 [95% CI: 0.64-0.96]; P = 0.021), and cardiovascular death or recurrent HHF (HR: 0.82 [95% CI: 0.72-0.95]; P = 0.006). The risk of outcomes increased across baseline eGFR and UACR categories; lowest incidences were seen in patients with an eGFR ≥60 mL/min/1.73 m2 and a UACR <300 mg/g. Finerenone improved HF outcomes irrespective of baseline eGFR and/or UACR categories (all P interaction values >0.10). Conclusions: Compared with placebo, finerenone improved HF-related outcomes in patients with CKD and T2D, with consistent benefits across eGFR and/or UACR categories. (Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease [FIDELIO-DKD], NCT02540993; Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and the Clinical Diagnosis of Chronic Kidney Disease [FIGARO-DKD], NCT02545049).
dc.eprint.versionFinal published version
dc.identifier.citationFilippatos G, Anker SD, Pitt B, et al. Finerenone and Heart Failure Outcomes by Kidney Function/Albuminuria in Chronic Kidney Disease and Diabetes [published correction appears in JACC Heart Fail. 2023 Aug;11(8 Pt 1):1034-1035]. JACC Heart Fail. 2022;10(11):860-870. doi:10.1016/j.jchf.2022.07.013
dc.identifier.urihttps://hdl.handle.net/1805/41259
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.jchf.2022.07.013
dc.relation.journalJACC: Heart Failure
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePublisher
dc.subjectAlbuminuria
dc.subjectChronic kidney disease
dc.subjectEstimated glomerular filtration rate
dc.subjectFinerenone
dc.subjectHeart failure
dc.subjectMineralocorticoid receptor antagonist
dc.titleFinerenone and Heart Failure Outcomes by Kidney Function/Albuminuria in Chronic Kidney Disease and Diabetes
dc.typeArticle
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