Electrical ventricular remodeling in dilated cardiomyopathy

Ventricular arrhythmias contribute significantly to morbidity and mortality in patients with heart failure (HF). Pathomechanisms underlying arrhythmogenicity in patients with structural heart disease and impaired cardiac function include myocardial fibrosis and the remodeling of ion channels, affect...

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Hauptverfasser: Mages, Christine (VerfasserIn) , Gampp, Heike (VerfasserIn) , Syren, Pascal (VerfasserIn) , Rahm, Ann-Kathrin (VerfasserIn) , André, Florian (VerfasserIn) , Frey, Norbert (VerfasserIn) , Lugenbiel, Patrick (VerfasserIn) , Thomas, Dierk (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 15 October 2021
In: Cells
Year: 2021, Jahrgang: 10, Heft: 10, Pages: 1-14
ISSN:2073-4409
DOI:10.3390/cells10102767
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/cells10102767
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/2073-4409/10/10/2767
Volltext
Verfasserangaben:Christine Mages, Heike Gampp, Pascal Syren, Ann-Kathrin Rahm, Florian André, Norbert Frey, Patrick Lugenbiel and Dierk Thomas

MARC

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520 |a Ventricular arrhythmias contribute significantly to morbidity and mortality in patients with heart failure (HF). Pathomechanisms underlying arrhythmogenicity in patients with structural heart disease and impaired cardiac function include myocardial fibrosis and the remodeling of ion channels, affecting electrophysiologic properties of ventricular cardiomyocytes. The dysregulation of ion channel expression has been associated with cardiomyopathy and with the development of arrhythmias. However, the underlying molecular signaling pathways are increasingly recognized. This review summarizes clinical and cellular electrophysiologic characteristics observed in dilated cardiomyopathy (DCM) with ionic and structural alterations at the ventricular level. Furthermore, potential translational strategies and therapeutic options are highlighted. 
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