Effects of Aficamten on cardiac contractility in a feline translational model of hypertrophic cardiomyopathy
Author
Sharpe, A.N.Oldach, M.S.
Rivas, V.N.
Kaplan, J.L.
Walker, A.L.
Kovacs, S.L.
Hwee, D.T.
Cremin, P.
Morgan, B.P.
Malik, F.I.
Harris, S.P.
Stern, J.A.
Affiliation
Department of Cellular and Molecular Medicine, University of ArizonaIssue Date
2023-01-02
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Nature ResearchCitation
Sharpe, A. N., Oldach, M. S., Rivas, V. N., Kaplan, J. L., Walker, A. L., Kovacs, S. L., ... & Stern, J. A. (2023). Effects of Aficamten on cardiac contractility in a feline translational model of hypertrophic cardiomyopathy. Scientific Reports, 13(1), 32.Journal
Scientific ReportsRights
© The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Hypertrophic cardiomyopathy (HCM) is the most prevalent inherited cardiac disease in humans and cats and lacks efficacious pharmacologic interventions in the preclinical phase of disease. LV outflow tract obstruction (LVOTO) is commonly observed in HCM-affected patients and is a primary driver of heart failure symptoms and reduced quality of life. Novel small-molecule cardiac myosin inhibitors target actin-myosin interactions to alleviate overactive protein interactions. A prospective, randomized, controlled cross-over study was performed to evaluate pharmacodynamic effects of two doses (0.3 and 1 mg/kg) of a next-in-class cardiac myosin inhibitor, aficamten (CK-3773274, CK-274), on cardiac function in cats with the A31P MYBPC3 mutation and oHCM. Dose-dependent reductions in LV systolic function, LVOT pressure gradient, and isovolumetric relaxation times compared to baseline were observed. Promising beneficial effects of reduced systolic function warrant further studies of this next-in-class therapeutic to evaluate the benefit of long-term administration in this patient population. © 2022, The Author(s).Note
Open access journalISSN
2045-2322PubMed ID
36593243Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1038/s41598-022-26630-z
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Except where otherwise noted, this item's license is described as © The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License.
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