FIDELIO study: significance and place of finerenone as nonsteroidal mineralocorticoid receptor antagonist in therapy of patients with chronic kidney disease in type 2 diabetes
https://doi.org/10.14341/DM13107
Abstract
Patients with diabetes mellitus and renal pathology are at high risk of developing end-stage kidney disease (ESKD) and cardiovascular disease (CVD), including atrial fibrillation as an life-threatening condition. The intense annual increase in patients with diabetes mellitus, mainly due to the patients with type 2 diabetes mellitus (T2D), and diabetic nephropathy sets a new goal for researchers to expand the range of drugs with cardio- and nephroprotective effects to offset the residual risks of development and progression of chronic kidney disease (CKD) and CVD in this cohort of patients. One of such drugs is finerenone — a novel selective non-steroidal mineralocorticoid receptor (MR) antagonist (MRA), hyperactivation of which mediates renal inflammation and fibrosis, cardiac remodeling and changes in its structural and electrical characteristics. This review presents the results of the sub-analysis of FIDELIO devoted to the mechanism of drug action, the finerenone efficacy evaluation, its comparison with the efficacy of sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists with already proven organoprotective properties with respect to reducing the risk of renal and cardiovascular endpoints.
About the Authors
M. S. ShamkhalovaRussian Federation
Minara S. Shamhalova, MD, PhD
Moscow
O. Yu. Sukhareva
Russian Federation
Olga Y. Sukhareva, MD, PhD
Moscow
M. I. Yevloyeva
Russian Federation
Madina I. Yevloyeva, MD, PhD student
Moscow
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Supplementary files
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1. Figure 1. FIDELIO main results for primary renal and key secondary endpoints [6]. | |
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2. Figure 2. Change in estimated glomerular filtration rate in the finerenone and placebo groups. | |
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3. Figure 3. Effects of finerenone on the risk of developing atrial fibrillation and cardiorenal effects depending on the presence of atrial fibrillation in history: a. Primary composite renal endpoint: time to development of end-stage renal disease, sustained decline in estimated glomerular filtration rate by ≥40% from baseline, or death from renal causes. b. Key secondary composite CV CT: time to death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure. | |
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4. Figure 4. Impact of differences in combined endpoints and characteristics of included patients on the therapeutic effect magnitude: a — FIDELIO did not include patients with eGFR >75 ml/min/1.73 m2; b — p-value was not calculated because inflation analysis was carried out; c — combined cardiorenal CT: time to development of ESRD, sustained decline in eGFR by ≥57%, death from renal causes, death from CV causes. | |
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Review
For citations:
Shamkhalova M.S., Sukhareva O.Yu., Yevloyeva M.I. FIDELIO study: significance and place of finerenone as nonsteroidal mineralocorticoid receptor antagonist in therapy of patients with chronic kidney disease in type 2 diabetes. Diabetes mellitus. 2023;26(6):603-614. (In Russ.) https://doi.org/10.14341/DM13107

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