Key result
Finerenone slows diabetic nephropathy progression and reduces cardiovascular morbidity in CKD.
Why the study?
Traditional MRAs for CKD were infrequently used with ACE inhibitors or ARBs due to hyperkalemia risk, motivating an overview of finerenone following its 2021 FDA approval.
Does finerenone improve outcomes in patients with chronic kidney disease and diabetic nephropathy?
Does finerenone improve outcomes in patients with chronic kidney disease and diabetic nephropathy?
This review highlights the pharmacological properties and clinical utility of finerenone as an effective treatment for chronic kidney disease and diabetic nephropathy.
Answers are grounded in this paper and cite their sources.
May support finerenone in diabetic CKD; leaves open need for confirmatory RCTs before practice change.
BACKGROUND: The most common cause of chronic kidney disease (CKD) is diabetic nephropathy (DN). Primarilymineralocorticoid receptor antagonists (MRAs) (spironolactone and eplerenone), angiotensin-converting enzyme inhibitors or angiotensin receptor blockers were used for the treatment of CKD, but due to the high risk of hyperkalaemia, the combination was infrequently used. Currently after approval by FDA in 2021, finerenone was found to be effective in the treatment of CKD. Finerenone slowdowns the progression of diabetic nephropathy and lessens the cardiovascular morbidity in DN patients. OBJECTIVE: The main objective of this review article is to provide a comprehensive and insightful overview of the role of finerenone by mainly focusing on its pharmacological properties, toxicity, uses, bioanalytical technique used for determination, and treatment options. MATERIALS AND METHOD: Finerenone works by inhibiting the action of the mineralocorticoid receptor. Finerenone is quickly absorbed from the digestive tract after oral treatment and achieves peak plasma concentrations in 1-2 hours. RESULT: Finerenone is actively metabolized through oxidation, epoxidation substitution, and direct hydroxylation. Elimination of finerenone is done through urine and feces. Determination of finerenone can be done through HPLC-MS and LSC. CONCLUSION: The present review covers the complete picture of ADME properties, bioanalytical techniques, clinical trials, toxicity, and possible avenues in this arena. Finerenone is effective compared to other mineralocorticoid receptor-like spironolactone and eplerenone, for the treatment of chronic kidney disease.
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Rana et al. (2024) conducted a review in Chronic kidney disease and diabetic nephropathy. Finerenone was evaluated. Finerenone is an effective mineralocorticoid receptor antagonist for the treatment of chronic kidney disease that slows the progression of diabetic nephropathy and lessens cardiovascular morbidity.
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