Ivabradine in the Management of COVID-19-related Cardiovascular Complications: A Perspective.


Journal

Current pharmaceutical design
ISSN: 1873-4286
Titre abrégé: Curr Pharm Des
Pays: United Arab Emirates
ID NLM: 9602487

Informations de publication

Date de publication:
2022
Historique:
received: 29 09 2021
accepted: 02 02 2022
pubmed: 30 3 2022
medline: 19 8 2022
entrez: 29 3 2022
Statut: ppublish

Résumé

Besides acute respiratory distress syndrome, acute cardiac injury is a major complication in severe coronavirus disease 2019 (COVID-19) and is associated with a poor clinical outcome. Acute cardiac injury with COVID-19 can be of various etiologies, including myocardial ischemia or infarction and myocarditis, and may compromise cardiac function, resulting in acute heart failure or cardiogenic shock. Systemic inflammatory response increases heart rate (HR), which disrupts the myocardial oxygen supply/demand balance and worsens cardiac energy efficiency, thus further deteriorating the cardiac performance of the injured myocardium. In fact, the combination of elevated resting HR and markers of inflammation synergistically predicts adverse cardiovascular prognosis. Thus, targeted HR reduction may potentially be of benefit in cardiovascular pathologies associated with COVID-19. Ivabradine is a drug that selectively reduces HR via If current inhibition in the sinoatrial node without a negative effect on inotropy. Besides selective HR reduction, ivabradine was found to exert various beneficial pleiotropic effects, either HR-dependent or HR-independent, including anti-inflammatory, anti-atherosclerotic, anti-oxidant and antiproliferative actions and the attenuation of endothelial dysfunction and neurohumoral activation. Cardioprotection by ivabradine has already been indicated in cardiovascular pathologies that are prevalent with COVID-19, including myocarditis, acute coronary syndrome, cardiogenic shock or cardiac dysautonomia. Here, we suggest that ivabradine may be beneficial in the management of COVID-19- related cardiovascular complications.

Identifiants

pubmed: 35345992
pii: CPD-EPUB-121912
doi: 10.2174/1381612828666220328114236
doi:

Substances chimiques

Benzazepines 0
Ivabradine 3H48L0LPZQ

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1581-1588

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Tomas Baka (T)

Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic.

Kristina Repova (K)

Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic.

Ivan Luptak (I)

Cardiovascular Medicine Section, Boston University School of Medicine, Boston, MA, USA.
Myocardial Biology Unit, Boston University School of Medicine, Boston, MA, USA.

Fedor Simko (F)

Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic.
3rd Department of Internal Medicine, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic.
Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of Sciences, Bratislava, Slovak Republic.

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Classifications MeSH