Literature DB >> 18634915

Catecholaminergic polymorphic ventricular tachycardia.

Nian Liu1, Yanfei Ruan, Silvia G Priori.   

Abstract

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a highly malignant form of arrhythmogenic disorder characterized by exercise- or emotional-induced polymorphic ventricular tachycardia in the absence of detectable structural heart disease. Because of the typical pattern of arrhythmias (bidirectional ventricular tachycardia and the occurrence and severity of arrhythmia correlated well with exercise workload) during exercise stress test, CPVT can be identified promptly. Molecular genetic screening of the genes encoding the cardiac ryanodine receptor and calsequestrin is critical to confirm uncertain diagnosis of CPVT. With the exception of beta-blockers, no pharmacologic therapy of proven effectiveness is available: although beta-blockers reduce the occurrence of ventricular tachycardia, 30% of patients treated with beta-blockers still experience cardiac arrhythmias and eventually require implantable cardioverter defibrillator implantation to prevent cardiac arrest.

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Year:  2008        PMID: 18634915     DOI: 10.1016/j.pcad.2007.10.005

Source DB:  PubMed          Journal:  Prog Cardiovasc Dis        ISSN: 0033-0620            Impact factor:   8.194


  47 in total

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2.  A mathematical model of spontaneous calcium release in cardiac myocytes.

Authors:  Wei Chen; Gary Aistrup; J Andrew Wasserstrom; Yohannes Shiferaw
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-02-25       Impact factor: 4.733

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Journal:  Arq Bras Cardiol       Date:  2019-03       Impact factor: 2.000

Review 4.  Calsequestrin mutations and catecholaminergic polymorphic ventricular tachycardia.

Authors:  Michela Faggioni; Dmytro O Kryshtal; Björn C Knollmann
Journal:  Pediatr Cardiol       Date:  2012-03-16       Impact factor: 1.655

5.  Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young.

Authors:  David J Tester; Jaeger P Ackerman; John R Giudicessi; Nicholas C Ackerman; Marina Cerrone; Mario Delmar; Michael J Ackerman
Journal:  JACC Clin Electrophysiol       Date:  2018-11-01

6.  Purkinje cells from RyR2 mutant mice are highly arrhythmogenic but responsive to targeted therapy.

Authors:  Guoxin Kang; Steven F Giovannone; Nian Liu; Fang-Yu Liu; Jie Zhang; Silvia G Priori; Glenn I Fishman
Journal:  Circ Res       Date:  2010-07-01       Impact factor: 17.367

7.  Risk stratification in young patients with channelopathies.

Authors:  N Sreeram; U Trieschmann; M Khalil; M Emmel
Journal:  Indian Pacing Electrophysiol J       Date:  2010-06-05

8.  Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.

Authors:  Mette Nyegaard; Michael T Overgaard; Mads T Søndergaard; Marta Vranas; Elijah R Behr; Lasse L Hildebrandt; Jacob Lund; Paula L Hedley; A John Camm; Göran Wettrell; Inger Fosdal; Michael Christiansen; Anders D Børglum
Journal:  Am J Hum Genet       Date:  2012-10-05       Impact factor: 11.025

9.  Modeling a ryanodine receptor N-terminal domain connecting the central vestibule and the corner clamp region.

Authors:  Li Zhu; Xiaowei Zhong; S R Wayne Chen; Nilesh Banavali; Zheng Liu
Journal:  J Biol Chem       Date:  2012-11-30       Impact factor: 5.157

Review 10.  Triadin regulation of the ryanodine receptor complex.

Authors:  Isabelle Marty
Journal:  J Physiol       Date:  2014-10-20       Impact factor: 5.182

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