Hereditary cardiac arrhythmia syndromes, such as catecholaminergic polymorphic ventricular tachycardia and long QT syndrome, are accompanied by maladaptive remodeling of calcium homeostasis which substantially increases arrhythmic risk.
Abstract Sudden cardiac death due to malignant ventricular arrhythmias remains the major cause of mortality in the postindustrial world. Defective intracellular Ca 2+ homeostasis has been well established as a key contributing factor to the enhanced propensity for arrhythmia in acquired cardiac disease, such as heart failure or diabetic cardiomyopathy. More recent advances provide a strong basis to the emerging view that hereditary cardiac arrhythmia syndromes are accompanied by maladaptive remodeling of Ca 2+ homeostasis which substantially increases arrhythmic risk. This brief review will focus on functional changes in elements of Ca 2+ handling machinery in cardiomyocytes that occur secondary to genetic mutations associated with catecholaminergic polymorphic ventricular tachycardia, and long QT syndrome.
Hamilton et al. (Wed,) conducted a review in Inherited cardiac arrhythmia syndromes. Hereditary cardiac arrhythmia syndromes, such as catecholaminergic polymorphic ventricular tachycardia and long QT syndrome, are accompanied by maladaptive remodeling of calcium homeostasis which substantially increases arrhythmic risk.
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