| Literature DB >> 19563351 |
Nagesh Chopra1, Björn C Knollmann.
Abstract
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare inherited disease characterized by physical or emotional stress-induced ventricular arrhythmias in the absence of any structural heart disease or QT prolongation. Thus far, mutations in genes encoding the sarcoplasmic reticulum Ca(2+) release channel (RYR2) and the sarcoplasmic reticulum Ca(2+) binding protein cardiac calsequestrin (CASQ2) have been identified in CPVT patients. Here, we review the role of cardiac calsequestrin in health and disease, with a particular focus on how calsequestrin deficiency can cause arrhythmia susceptibility. Clinical implications and a promising new drug therapy for CPVT are discussed.Entities:
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Year: 2009 PMID: 19563351 DOI: 10.1111/j.1540-8167.2009.01531.x
Source DB: PubMed Journal: J Cardiovasc Electrophysiol ISSN: 1045-3873