Differentiation between emerging non-steroidal and established steroidal mineralocorticoid receptor antagonists: head-to-head comparisons of pharmacological and clinical characteristics.

AZD9977 KBP-5074 cardiorenal disease chronic kidney disease esaxerenone finerenone heart failure hypertension non-steroidal mineralocorticoid receptor antagonists

Journal

Expert opinion on investigational drugs
ISSN: 1744-7658
Titre abrégé: Expert Opin Investig Drugs
Pays: England
ID NLM: 9434197

Informations de publication

Date de publication:
Nov 2021
Historique:
pubmed: 12 11 2021
medline: 11 1 2022
entrez: 11 11 2021
Statut: ppublish

Résumé

Mineralocorticoid receptor (MR) antagonists (MRAs) provide cardiorenal protection. However steroidal MRAs might induce hyperkalemia and sex hormone-related adverse effects. Several novel non-steroidal MRAs are being developed that are highly selective for the MR and may have an improved safety profile. This narrative review summarizes data from head-to-head comparisons of emerging non-steroidal MRAs with older steroidal MRAs, including pharmacological characteristics, pharmacokinetic properties, clinical outcomes, and safety, and highlights similarities and differences between emerging agents and established steroidal MRAs. Head-to-head comparisons in phase 2 trials suggest that the new non-steroidal MRAs exhibit at least equivalent efficacy to steroidal MRAs but may have a better safety profile in patients with heart failure and/or kidney disease. When also taking into account data from recent phase 3 placebo-controlled trials, these novel non-steroidal MRAs have the potential to provide a cardiorenal benefit above that of current optimized standard-of-care treatment in a high-risk population with reduced renal function, and with a lower risk of hyperkalemia. To optimize therapy, further research is needed to clarify the molecular differences in the mode of action of non-steroidal MRAs versus steroidal MRAs, and biomarkers that are predictive of MRA response need to be identified and validated.

Identifiants

pubmed: 34758679
doi: 10.1080/13543784.2021.2002844
doi:

Substances chimiques

Mineralocorticoid Receptor Antagonists 0
Steroids 0

Types de publication

Comparative Study Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1141-1157

Auteurs

Jonatan Barrera-Chimal (J)

Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Unidad de Investigación UNAM-INC, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.

Peter Kolkhof (P)

Heart and Vascular Diseases, R&D Preclinical Research, Bayer AG, Germany.

Ixchel Lima-Posada (I)

Centre de Recherche Des Cordeliers, Sorbonne Université, Université de Paris, Paris, France.

Alexandre Joachim (A)

Normandy University, University of Caen Normandy, Centre Hospitalier Universitaire (CHU) de Caen Normandie, Department of Pharmacology, Ea 4650, Signalisation, Électrophysiologie Et Imagerie Des Lésions d'Ischémie-Reperfusion Myocardique, Caen, France.

Patrick Rossignol (P)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques Plurithématique - 1433, and Inserm U1116; Chru Nancy; F-crin Ini-crct, Nancy, France.

Frederic Jaisser (F)

Centre de Recherche Des Cordeliers, Sorbonne Université, Université de Paris, Paris, France.
Université de Lorraine, Inserm, Centre d'Investigations Cliniques Plurithématique - 1433, and Inserm U1116; Chru Nancy; F-crin Ini-crct, Nancy, France.

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Classifications MeSH