Literature DB >> 17275752

Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition.

Philippe Chevalier1, Chloé Bellocq, Gilles Millat, Eric Piqueras, Franck Potet, Jean-Jacques Schott, Isabelle Baró, Hervé Lemarec, Jacques Barhanin, Robert Rousson, Claire Rodriguez-Lafrasse.   

Abstract

BACKGROUND: The prevalence of genetic risk factors has not been systematically evaluated in the setting of complete atriventricular (AV) block complicated by long QT syndrome (LQTS).
OBJECTIVE: This study was performed to determine to what extent acquired LQTS in the context of AV block has a genetic substrate.
METHODS: Among 420 recipients of pacemakers implanted over a 3-year period, we identified retrospectively 29 patients with complete AV block and a QT interval >600 ms in duration. A second study group included 22 randomly selected patients who had AV block and a QT interval <600 ms. Normal controls were 100 consecutive individuals without medical history. Genetic studies screening for HERG, KCNQ1 KCNE1, KCNE2, and SCN5A mutations were performed.
RESULTS: We identified four mutations on genes encoding potassium channels in five patients with AV block and acquired LQTS. These mutations were not found among patients with AV block and a QT interval <600 ms in duration or in healthy volunteers. Functional expression of three HERG mutations (R328C, R696C, and R1047L) had a dominant negative effect on wild-type I(Kr). One KCNE2 mutation (R77W) identified in a patient treated with flecainide did not alter I(Kr).
CONCLUSIONS: This study showed that complete AV block complicated by LQTS was associated with HERG mutations in 17% of cases. Further studies are needed to identify factors, genetic or environmental, which may be implicated in bradycardia-related abnormalities of ventricular repolarization.

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Year:  2006        PMID: 17275752     DOI: 10.1016/j.hrthm.2006.10.004

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  10 in total

1.  Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors.

Authors:  Jeffrey S Bennett; Madison Bernhardt; Kim L McBride; Shalini C Reshmi; Erik Zmuda; Naomi J Kertesz; Vidu Garg; Sara Fitzgerald-Butt; Anna N Kamp
Journal:  Pediatr Cardiol       Date:  2019-09-18       Impact factor: 1.655

2.  Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates.

Authors:  Rajesh N Subbiah; Michael H Gollob; Lorne J Gula; Robert W Davies; Peter Leong-Sit; Allan C Skanes; Raymond Yee; George J Klein; Andrew D Krahn
Journal:  Can J Cardiol       Date:  2010-04       Impact factor: 5.223

3.  Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

Authors:  Elena Burashnikov; Ryan Pfeiffer; Héctor Barajas-Martinez; Eva Delpón; Dan Hu; Mayurika Desai; Martin Borggrefe; Michel Häissaguerre; Ronald Kanter; Guido D Pollevick; Alejandra Guerchicoff; Ruben Laiño; Mark Marieb; Koonlawee Nademanee; Gi-Byoung Nam; Roberto Robles; Rainer Schimpf; Dwight D Stapleton; Sami Viskin; Stephen Winters; Christian Wolpert; Samuel Zimmern; Christian Veltmann; Charles Antzelevitch
Journal:  Heart Rhythm       Date:  2010-10-14       Impact factor: 6.343

Review 4.  KCNH2 pharmacogenomics summary.

Authors:  Connie Oshiro; Caroline F Thorn; Dan M Roden; Teri E Klein; Russ B Altman
Journal:  Pharmacogenet Genomics       Date:  2010-12       Impact factor: 2.089

5.  Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.

Authors:  Holger Herlyn; Ulrich Zechner; Franz Oswald; Arne Pfeufer; Hans Zischler; Thomas Haaf
Journal:  BMC Evol Biol       Date:  2009-08-06       Impact factor: 3.260

Review 6.  Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.

Authors:  Zahurul A Bhuiyan; Safar Al-Shahrani; Jumana Al-Aama; Arthur A M Wilde; Tarek S Momenah
Journal:  Front Pediatr       Date:  2013-11-20       Impact factor: 3.418

7.  Unravelling Atrioventricular Block Risk in Inflammatory Diseases: Systemic Inflammation Acutely Delays Atrioventricular Conduction via a Cytokine-Mediated Inhibition of Connexin43 Expression.

Authors:  Pietro Enea Lazzerini; Maurizio Acampa; Michael Cupelli; Alessandra Gamberucci; Ujala Srivastava; Claudio Nanni; Iacopo Bertolozzi; Francesca Vanni; Alessandro Frosali; Anna Cantore; Alessandra Cartocci; Antonio D'Errico; Viola Salvini; Riccardo Accioli; Decoroso Verrengia; Fabio Salvadori; Aleksander Dokollari; Massimo Maccherini; Nabil El-Sherif; Franco Laghi-Pasini; Pier Leopoldo Capecchi; Mohamed Boutjdir
Journal:  J Am Heart Assoc       Date:  2021-10-29       Impact factor: 5.501

8.  Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.

Authors:  Christian Trolle; Kristian H Mortensen; Lisbeth N Pedersen; Agnethe Berglund; Henrik K Jensen; Niels H Andersen; Claus H Gravholt
Journal:  PLoS One       Date:  2013-07-25       Impact factor: 3.240

9.  Long QT syndrome in South Africa: the results of comprehensive genetic screening.

Authors:  Paula L Hedley; Glenda A Durrheim; Firzana Hendricks; Althea Goosen; Cathrine Jespersgaard; Birgitte Støvring; Tam T Pham; Michael Christiansen; Paul A Brink; Valerie A Corfield
Journal:  Cardiovasc J Afr       Date:  2013-07       Impact factor: 1.167

10.  Torsade de Pointes Triggered by Early Ventricular Escape Beats in a Patient with Complete Atrioventricular Block.

Authors:  Erkan Yildirim; Baris Bugan; Suat Gormel; Uygar Cagdas Yuksel; Murat Celik; Yalcin Gokoglan; Serdar Firtina; Sinan Iscen; Emre Yalcinkaya; Ugur Kucuk; Hasan Kutsi Kabul
Journal:  Case Rep Cardiol       Date:  2016-04-06
  10 in total

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