Cardiac Calsequestrin: The New Kid on the Block in Arrhythmias
Article first published online: 26 JUN 2009
DOI: 10.1111/j.1540-8167.2009.01531.x
© 2009 Wiley Periodicals, Inc.
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How to Cite
CHOPRA, N. and KNOLLMANN, B. C. (2009), Cardiac Calsequestrin: The New Kid on the Block in Arrhythmias. Journal of Cardiovascular Electrophysiology, 20: 1179–1185. doi: 10.1111/j.1540-8167.2009.01531.x
Publication History
- Issue published online: 6 OCT 2009
- Article first published online: 26 JUN 2009
- Manuscript received 16 March 2009; Revised manuscript received 28 April 2009; Accepted for publication 30 April 2009.
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Keywords:
- cardiac calsequestrin;
- ventricular tachycardia;
- sarcoplasmic reticulum;
- catecholaminergic polymorphic ventricular tachycardia;
- excitation-contraction coupling
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 Ca2+ release channel (RYR2) and the sarcoplasmic reticulum Ca2+ 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.

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