Literature DB >> 27711072

Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.

Jonas Ghouse1,2, Christian T Have3, Morten W Skov1,2, Laura Andreasen1,2, Gustav Ahlberg1,2, Jonas B Nielsen1,2,4, Tea Skaaby5, Søren-Peter Olesen1, Niels Grarup3, Allan Linneberg5,6,7, Oluf Pedersen3, Henrik Vestergaard3, Stig Haunsø1,2,7, Jesper H Svendsen1,2,7, Torben Hansen3, Jørgen K Kanters8, Morten S Olesen1,2.   

Abstract

PURPOSE: We investigated whether Brugada syndrome (BrS)-associated variants identified in the general population have an effect on J-point elevation as well as whether carriers of BrS variants were more prone to experience syncope and malignant ventricular arrhythmia and had increased mortality compared with noncarriers.
METHODS: All BrS-associated variants were identified using the Human Gene Mutation Database (HGMD). Individuals were randomly selected from a general population study using whole-exome sequencing data (n = 870) and genotype array data (n = 6,161) and screened for BrS-associated variants. Electrocardiograms (ECG) were analyzed electronically, and data on syncope, ventricular arrhythmias, and mortality were obtained from administrative health-care registries.
RESULTS: In HGMD, 382 BrS-associated genetic variants were identified. Of these, 28 variants were identified in the study cohort. None of the carriers presented with type 1 BrS ECG pattern. Mean J-point elevation in V1 and V2 were within normal guideline limits for carriers and noncarriers. There was no difference in syncope susceptibility (carriers 8/624; noncarriers 98/5,562; P = 0.51), ventricular arrhythmia (carriers 4/620; noncarriers 9/5,524; P = 0.24), or overall mortality (hazard ratio 0.93, 95% CI 0.63-1.4).
CONCLUSIONS: Our data indicate that a significant number of BrS-associated variants are not the monogenic cause of BrS.Genet Med advance online publication 06 October 2016.

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Year:  2016        PMID: 27711072     DOI: 10.1038/gim.2016.151

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  8 in total

1.  The Brazilian Society of Cardiology and Brazilian Society of Exercise and Sports Medicine Updated Guidelines for Sports and Exercise Cardiology - 2019.

Authors:  Nabil Ghorayeb; Ricardo Stein; Daniel Jogaib Daher; Anderson Donelli da Silveira; Luiz Eduardo Fonteles Ritt; Daniel Fernando Pellegrino Dos Santos; Ana Paula Rennó Sierra; Artur Haddad Herdy; Claúdio Gil Soares de Araújo; Cléa Simone Sabino de Souza Colombo; Daniel Arkader Kopiler; Filipe Ferrari Ribeiro de Lacerda; José Kawazoe Lazzoli; Luciana Diniz Nagem Janot de Matos; Marcelo Bichels Leitão; Ricardo Contesini Francisco; Rodrigo Otávio Bougleux Alô; Sérgio Timerman; Tales de Carvalho; Thiago Ghorayeb Garcia
Journal:  Arq Bras Cardiol       Date:  2019-03       Impact factor: 2.000

Review 2.  Paediatric genomics: diagnosing rare disease in children.

Authors:  Caroline F Wright; David R FitzPatrick; Helen V Firth
Journal:  Nat Rev Genet       Date:  2018-02-05       Impact factor: 53.242

3.  Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts.

Authors:  Christian Paludan-Müller; Jonas Ghouse; Oliver B Vad; Cecilie B Herfelt; Pia Lundegaard; Gustav Ahlberg; Nicole Schmitt; Jesper H Svendsen; Stig Haunsø; Henning Bundgaard; Torben Hansen; Jørgen K Kanters; Morten S Olesen
Journal:  Eur J Hum Genet       Date:  2019-05-01       Impact factor: 4.246

4.  Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation.

Authors:  Yuya Kobayashi; Shan Yang; Keith Nykamp; John Garcia; Stephen E Lincoln; Scott E Topper
Journal:  Genome Med       Date:  2017-02-06       Impact factor: 11.117

5.  Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.

Authors:  Christopher M Haggerty; Cynthia A James; Hugh Calkins; Crystal Tichnell; Joseph B Leader; Dustin N Hartzel; Christopher D Nevius; Sarah A Pendergrass; Thomas N Person; Marci Schwartz; Marylyn D Ritchie; David J Carey; David H Ledbetter; Marc S Williams; Frederick E Dewey; Alexander Lopez; John Penn; John D Overton; Jeffrey G Reid; Matthew Lebo; Heather Mason-Suares; Christina Austin-Tse; Heidi L Rehm; Brian P Delisle; Daniel J Makowski; Vishal C Mehra; Michael F Murray; Brandon K Fornwalt
Journal:  Genet Med       Date:  2017-05-04       Impact factor: 8.822

6.  Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.

Authors:  Oliver Bundgaard Vad; Yannan Yan; Federico Denti; Gustav Ahlberg; Lena Refsgaard; Sofia Hammami Bomholtz; Joana Larupa Santos; Simon Rasmussen; Stig Haunsø; Jesper Hastrup Svendsen; Ingrid Elizabeth Christophersen; Nicole Schmitt; Morten Salling Olesen; Bo Hjorth Bentzen
Journal:  Front Genet       Date:  2022-01-28       Impact factor: 4.599

7.  Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest.

Authors:  Laura Andreasen; Jonas Ghouse; Morten W Skov; Christian T Have; Gustav Ahlberg; Peter V Rasmussen; Allan Linneberg; Oluf Pedersen; Pyotr G Platonov; Stig Haunsø; Jesper H Svendsen; Torben Hansen; Jørgen K Kanters; Morten S Olesen
Journal:  Front Physiol       Date:  2018-07-10       Impact factor: 4.566

8.  Meta-Analysis of Risk Stratification of SCN5A With Brugada Syndrome: Is SCN5A Always a Marker of Low Risk?

Authors:  Yihan Yang; Dan Hu; Frederic Sacher; Kengo F Kusano; Xinye Li; Hector Barajas-Martinez; Mélèze Hocini; Yanda Li; Yonghong Gao; Hongcai Shang; Yanwei Xing
Journal:  Front Physiol       Date:  2019-02-19       Impact factor: 4.566

  8 in total

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