Catecholaminergic polymorphic ventricular tachycardia overview
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT is a rare inherited arrhythmogenic disorder characterized by syncopal attacks, ventricular arrhythmias, and even sudden cardiac death, mostly in young patients. It is caused by mutations in calcium handling proteins such as RyR2 and CASQ2 within the sarcoplasmic reticulum, which results in ventricular arrhythmias in the setting of a high adrenergic tone such as during physical exercise or strong emotions. Since it is caused by mutations in genes encoding for channel-proteins that regulate cardiac electrical activity, CPVT is referred to as a channelopathy. There are no associated structural abnormalities of the heart in catecholaminergic polymorphic ventricular tachycardia.
Historical Perspective
Catecholaminergic polymorphic ventricular tachycardia (CPVT) was first described by Reid et al in 1975. It was described as a familial cardiac arrhythmia that occurs in patients with structurally normal heart and causes exercise or emotion triggered syncope and sudden death with a distinguishing pattern of ventricular and supraventricular arrhythmias. In 2001, cardiac ryanodine receptor gene (RyR2) mutations were first implicated in the pathogenesis of catecholaminergic polymorphic ventricular tachycardia (CPVT). Subsequent experimental studies demonstrated that the abnormal calcium release from the sarcoplasmic reticulum caused arrhythmias mediated by delayed afterdepolarizations and triggered activity.
Classification
Catecholaminergic polymorphic ventricular tachycardia can be classified based upon the underlying pathogenic mutation.
Pathophysiology
Catecholaminergic polymorphic ventricular tachycardia is caused by mutations in genes encoding channel proteins that regulate the cardiac electrical function, resulting in inappropriate calcium leak from the sarcoplasmic reticulum during electrical diastole and thus leading to triggered arrhythmias, in the absence of structural cardiac abnormalities. CPVT is thus an inherited disorder and may have both autosomal dominant and autosomal recessive pattern of inheritance. Genes associated with CPVT include RYR2, CASQ2, CALM1 and TRDN.
Causes
Catecholaminergic polymorphic ventricular tachycardia is a genetic disorder. It is caused by mutations in the genes such as RYR2, CASQ2, CALM1 and TRDN.
Differentiating Catecholaminergic polymorphic ventricular tachycardia from other Diseases
Catecholaminergic polymorphic ventricular tachycardia must be differentiated from Arrhythmogenic right ventricular dysplasia, Short-coupled ventricular tachycardia (SC-torsade de pointes [TdP]), Long QT syndrome and Andersen-Tawil syndrome.
Epidemiology and Demographics
Catecholaminergic polymorphic ventricular tachycardia is a rare disorder with the prevalence estimated to be 1 per 10,000 individuals. CPVT is more common among young individuals.
Risk factors
Possible risk factors in the development of catecholaminergic polymorphic ventricular tachycardia (CPVT) include young age, exercise, stress, family history of syncope or sudden death, and family history of CPVT.
Screening
There is insufficient evidence to recommend routine screening for Catecholaminergic polymorphic ventricular tachycardia. But screening among relatives is indicated when a likely pathogenetic mutation is identified in clinically affected index cases. Screening methods for CPVT are exercise stress testing and genetic testing.
Natural History, Complications and Prognosis
If left untreated, approximately 30% of patients experience at least one cardiac arrest and up to 80% one or more syncopal spells. Common complications of catecholaminergic polymorphic ventricular tachycardia include ventricular fibrillation, sudden cardiac arrest, and sudden cardiac death. Prognosis is generally poor, and the 10-year mortality of patients with catecholaminergic polymorphic ventricular tachycardia is approximately 40%.
Diagnosis
History and symptoms
Syncope triggered by exercise or emotion is the initial manifestation in the majority of the cases of catecholaminergic polymorphic ventricular tachycardia. Sudden cardiac death during exercise or emotion may also be the initial manifestation in a relevant proportion of cases. Most of the patients have a positive family history of CPVT or sudden cardiac death.
Physical examination
Patients with catecholaminergic polymorphic ventricular tachycardia usually appear normal. Physical examination should include thorough cardiovascular examination, lung examination, and close monitoring of vital signs.
Laboratory findings
There are no diagnostic laboratory findings associated with catecholaminergic polymorphic ventricular tachycardia.
Electrocardiogram
Catecholaminergic polymorphic ventricular tachycardia patients usually have a normal resting ECG. However, in a subset of patients, sinus bradycardia, prominent U-waves, and supraventricular arrhythmias are seen.
X-ray
There are no x-ray findings associated with catecholaminergic polymorphic ventricular tachycardia.
Echocardiography/Ultrasound
There are no echocardiography/ultrasound findings associated with catecholaminergic polymorphic ventricular tachycardia.
CT scan
There are no CT scan findings associated with catecholaminergic polymorphic ventricular tachycardia.
MRI
There are no MRI findings associated with catecholaminergic polymorphic ventricular tachycardia.
Other Imaging Findings
There are no other imaging findings associated with Catecholaminergic polymorphic ventricular tachycardia.
Treatment
Medical Therapy | Interventions | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies