Literature DB >> 16963070

Genotype-specific ECG patterns in long QT syndrome.

Wojciech Zareba1.   

Abstract

Different genetic types of the long QT syndrome (LQTS) are associated with distinct ECG manifestations, which relate to the type and magnitude of ion channel dysfunction. The QTc duration does not differentiate LQTS types, and therefore other static and dynamic ECG parameters reflecting changes in T wave morphology are used to describe phenotypic expression of different LQTS genotypes. LQT1 carriers usually have broad-based T waves, LQT2 carriers show low-amplitude T waves with high incidence of notches, and LQT3 carriers frequently have extended ST segment with relatively narrow peaked T wave. This phenotypic differentiation could be enhanced by quantifying additional ECG parameters reflecting components of repolarization morphology as well as to evaluate dynamics of repolarization parameters. Heart rate dependency and dynamic behavior of repolarization parameters differ by genotype and further show that genotype indicates ECG phenotype in patients with LQTS. However, there is a substantial variation in repolarization abnormalities observed in the same subject and in the members of the same family indicating large differences in gene penetrance. In conclusion, comprehensive analyses of static and dynamic features of repolarization provide unique opportunity to understand electrophysiology of cardiac repolarization.

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Mesh:

Year:  2006        PMID: 16963070     DOI: 10.1016/j.jelectrocard.2006.05.017

Source DB:  PubMed          Journal:  J Electrocardiol        ISSN: 0022-0736            Impact factor:   1.438


  16 in total

1.  Patient with syncope and LQTS carrying a mutation in the PAS domain of the hERG1 channel.

Authors:  Liliana Sintra Grilo; Jürg Schläpfer; Florence Fellmann; Hugues Abriel
Journal:  Ann Noninvasive Electrocardiol       Date:  2011-04       Impact factor: 1.468

2.  Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.

Authors:  Sven Zumhagen; Birgit Stallmeyer; Corinna Friedrich; Lars Eckardt; Guiscard Seebohm; Eric Schulze-Bahr
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2012-09-21

3.  Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.

Authors:  Julie Rutberg; Martin S Green; Robert M Gow; Michael T Geraghty; Christina Honeywell; John Ewen; David H Birnie; Anthony Tang; Robert Lemery; Michael H Gollob
Journal:  Can J Cardiol       Date:  2007-09       Impact factor: 5.223

4.  Long QT syndrome: A therapeutic challenge.

Authors:  Maully Shah; Christopher Carter
Journal:  Ann Pediatr Cardiol       Date:  2008-01

5.  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

6.  Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.

Authors:  Suraj Kapa; David J Tester; Benjamin A Salisbury; Carole Harris-Kerr; Manish S Pungliya; Marielle Alders; Arthur A M Wilde; Michael J Ackerman
Journal:  Circulation       Date:  2009-10-19       Impact factor: 29.690

Review 7.  Congenital Long QT syndrome and torsade de pointes.

Authors:  Nabil El-Sherif; Gioia Turitto; Mohamed Boutjdir
Journal:  Ann Noninvasive Electrocardiol       Date:  2017-07-02       Impact factor: 1.468

8.  Clinical presentation and course of long QT syndrome in Thai children.

Authors:  Ankavipar Saprungruang; Kanyalak Vithessonthi; Vidhavas La-Orkhun; Pornthep Lertsapcharoen; Apichai Khongphatthanayothin
Journal:  J Arrhythm       Date:  2015-05-28

9.  Genetic testing for long QT syndrome and the category of cardiac ion channelopathies.

Authors:  Stephen M Modell; David J Bradley; Michael H Lehmann
Journal:  PLoS Curr       Date:  2012-05-03

10.  Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2.

Authors:  Ewa Moric-Janiszewska; Joanna Głogowska-Ligus; Monika Paul-Samojedny; Ludmiła Węglarz; Grażyna Markiewicz-Łoskot; Lesław Szydłowski
Journal:  Arch Med Sci       Date:  2011-12-30       Impact factor: 3.318

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