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Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study
OBJECTIVE: Finerenone 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 trea...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271031/ https://www.ncbi.nlm.nih.gov/pubmed/35061867 http://dx.doi.org/10.2337/dc21-1944 |
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author | Rossing, Peter Burgess, Ellen Agarwal, Rajiv Anker, Stefan D. Filippatos, Gerasimos Pitt, Bertram Ruilope, Luis M. Gillard, Pieter MacIsaac, Richard J. Wainstein, Julio Joseph, Amer Brinker, Meike Roessig, Lothar Scott, Charlie Bakris, George L. |
author_facet | Rossing, Peter Burgess, Ellen Agarwal, Rajiv Anker, Stefan D. Filippatos, Gerasimos Pitt, Bertram Ruilope, Luis M. Gillard, Pieter MacIsaac, Richard J. Wainstein, Julio Joseph, Amer Brinker, Meike Roessig, Lothar Scott, Charlie Bakris, George L. |
author_sort | Rossing, Peter |
collection | PubMed |
description | OBJECTIVE: Finerenone 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 METHODS: Patients 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%. RESULTS: Of 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. CONCLUSIONS: Finerenone reduces kidney and cardiovascular outcome risk in patients with CKD and T2D, and risks appear consistent irrespective of HbA(1c) levels or insulin use. |
format | Online Article Text |
id | pubmed-9271031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-92710312022-10-22 Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study Rossing, Peter Burgess, Ellen Agarwal, Rajiv Anker, Stefan D. Filippatos, Gerasimos Pitt, Bertram Ruilope, Luis M. Gillard, Pieter MacIsaac, Richard J. Wainstein, Julio Joseph, Amer Brinker, Meike Roessig, Lothar Scott, Charlie Bakris, George L. Diabetes Care Emerging Therapies: Drugs and Regimens OBJECTIVE: Finerenone 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 METHODS: Patients 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%. RESULTS: Of 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. CONCLUSIONS: Finerenone reduces kidney and cardiovascular outcome risk in patients with CKD and T2D, and risks appear consistent irrespective of HbA(1c) levels or insulin use. American Diabetes Association 2022-04 2022-01-21 /pmc/articles/PMC9271031/ /pubmed/35061867 http://dx.doi.org/10.2337/dc21-1944 Text en © 2022 by the American Diabetes Association https://www.diabetesjournals.org/content/licenseReaders may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at https://www.diabetesjournals.org/journals/pages/license. |
spellingShingle | Emerging Therapies: Drugs and Regimens Rossing, Peter Burgess, Ellen Agarwal, Rajiv Anker, Stefan D. Filippatos, Gerasimos Pitt, Bertram Ruilope, Luis M. Gillard, Pieter MacIsaac, Richard J. Wainstein, Julio Joseph, Amer Brinker, Meike Roessig, Lothar Scott, Charlie Bakris, George L. Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study |
title | Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study |
title_full | Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study |
title_fullStr | Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study |
title_full_unstemmed | Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study |
title_short | Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes According to Baseline HbA(1c) and Insulin Use: An Analysis From the FIDELIO-DKD Study |
title_sort | finerenone in patients with chronic kidney disease and type 2 diabetes according to baseline hba(1c) and insulin use: an analysis from the fidelio-dkd study |
topic | Emerging Therapies: Drugs and Regimens |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271031/ https://www.ncbi.nlm.nih.gov/pubmed/35061867 http://dx.doi.org/10.2337/dc21-1944 |
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