Literature DB >> 24951663

Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.

Jared W Magnani, Jennifer A Brody, Bram P Prins, Dan E Arking, Honghuang Lin, Xiaoyan Yin, Ching-Ti Liu, Alanna C Morrison, Feng Zhang, Tim D Spector, Alvaro Alonso, Joshua C Bis, Susan R Heckbert, Thomas Lumley, Colleen M Sitlani, L Adrienne Cupples, Steven A Lubitz, Elsayed Z Soliman, Sara L Pulit, Christopher Newton-Cheh, Christopher J O'Donnell, Patrick T Ellinor, Emelia J Benjamin, Donna M Muzny, Richard A Gibbs, Jireh Santibanez, Herman A Taylor, Jerome I Rotter, Leslie A Lange, Bruce M Psaty, Rebecca Jackson, Stephen S Rich, Eric Boerwinkle, Yalda Jamshidi, Nona Sotoodehnia.   

Abstract

BACKGROUND: The cardiac sodium channel SCN5A regulates atrioventricular and ventricular conduction. Genetic variants in this gene are associated with PR and QRS intervals. We sought to characterize further the contribution of rare and common coding variation in SCN5A to cardiac conduction. METHODS AND
RESULTS: In Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study, we performed targeted exonic sequencing of SCN5A (n=3699, European ancestry individuals) and identified 4 common (minor allele frequency >1%) and 157 rare variants. Common and rare SCN5A coding variants were examined for association with PR and QRS intervals through meta-analysis of European ancestry participants from CHARGE, National Heart, Lung, and Blood Institute's Exome Sequencing Project (n=607), and the UK10K (n=1275) and by examining Exome Sequencing Project African ancestry participants (n=972). Rare coding SCN5A variants in aggregate were associated with PR interval in European and African ancestry participants (P=1.3×10(-3)). Three common variants were associated with PR and QRS interval duration among European ancestry participants and one among African ancestry participants. These included 2 well-known missense variants: rs1805124 (H558R) was associated with PR and QRS shortening in European ancestry participants (P=6.25×10(-4) and P=5.2×10(-3), respectively) and rs7626962 (S1102Y) was associated with PR shortening in those of African ancestry (P=2.82×10(-3)). Among European ancestry participants, 2 novel synonymous variants, rs1805126 and rs6599230, were associated with cardiac conduction. Our top signal, rs1805126 was associated with PR and QRS lengthening (P=3.35×10(-7) and P=2.69×10(-4), respectively) and rs6599230 was associated with PR shortening (P=2.67×10(-5)).
CONCLUSIONS: By sequencing SCN5A, we identified novel common and rare coding variants associated with cardiac conduction.
© 2014 American Heart Association, Inc.

Entities:  

Keywords:  electrocardiography; genomics

Mesh:

Substances:

Year:  2014        PMID: 24951663      PMCID: PMC4177904          DOI: 10.1161/CIRCGENETICS.113.000098

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN: 1942-3268


  46 in total

1.  A single Na(+) channel mutation causing both long-QT and Brugada syndromes.

Authors:  C Bezzina; M W Veldkamp; M P van Den Berg; A V Postma; M B Rook; J W Viersma; I M van Langen; G Tan-Sindhunata; M T Bink-Boelkens; A H van Der Hout; M M Mannens; A A Wilde
Journal:  Circ Res       Date:  1999 Dec 3-17       Impact factor: 17.367

2.  SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap.

Authors:  Andrew D Johnson; Robert E Handsaker; Sara L Pulit; Marcia M Nizzari; Christopher J O'Donnell; Paul I W de Bakker
Journal:  Bioinformatics       Date:  2008-10-30       Impact factor: 6.937

3.  Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro.

Authors:  Hiroshi Watanabe; Tao Yang; Dina Myers Stroud; John S Lowe; Louise Harris; Thomas C Atack; Dao W Wang; Susan B Hipkens; Brenda Leake; Lynn Hall; Sabina Kupershmidt; Nagesh Chopra; Mark A Magnuson; Naohito Tanabe; Björn C Knollmann; Alfred L George; Dan M Roden
Journal:  Circulation       Date:  2011-08-08       Impact factor: 29.690

4.  SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism.

Authors:  William P McNair; Gianfranco Sinagra; Matthew R G Taylor; Andrea Di Lenarda; Debra A Ferguson; Ernesto E Salcedo; Dobromir Slavov; Xiao Zhu; John H Caldwell; Luisa Mestroni
Journal:  J Am Coll Cardiol       Date:  2011-05-24       Impact factor: 24.094

5.  An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

Authors:  Jamie D Kapplinger; David J Tester; Marielle Alders; Begoña Benito; Myriam Berthet; Josep Brugada; Pedro Brugada; Véronique Fressart; Alejandra Guerchicoff; Carole Harris-Kerr; Shiro Kamakura; Florence Kyndt; Tamara T Koopmann; Yoshihiro Miyamoto; Ryan Pfeiffer; Guido D Pollevick; Vincent Probst; Sven Zumhagen; Matteo Vatta; Jeffrey A Towbin; Wataru Shimizu; Eric Schulze-Bahr; Charles Antzelevitch; Benjamin A Salisbury; Pascale Guicheney; Arthur A M Wilde; Ramon Brugada; Jean-Jacques Schott; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2009-10-08       Impact factor: 6.343

6.  Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

Authors:  Igor Splawski; Katherine W Timothy; Michihiro Tateyama; Colleen E Clancy; Alka Malhotra; Alan H Beggs; Francesco P Cappuccio; Giuseppe A Sagnella; Robert S Kass; Mark T Keating
Journal:  Science       Date:  2002-08-23       Impact factor: 47.728

7.  Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A).

Authors:  D Woodrow Benson; Dao W Wang; Macaira Dyment; Timothy K Knilans; Frank A Fish; Margaret J Strieper; Thomas H Rhodes; Alfred L George
Journal:  J Clin Invest       Date:  2003-10       Impact factor: 14.808

8.  A framework for variation discovery and genotyping using next-generation DNA sequencing data.

Authors:  Mark A DePristo; Eric Banks; Ryan Poplin; Kiran V Garimella; Jared R Maguire; Christopher Hartl; Anthony A Philippakis; Guillermo del Angel; Manuel A Rivas; Matt Hanna; Aaron McKenna; Tim J Fennell; Andrew M Kernytsky; Andrey Y Sivachenko; Kristian Cibulskis; Stacey B Gabriel; David Altshuler; Mark J Daly
Journal:  Nat Genet       Date:  2011-04-10       Impact factor: 38.330

9.  Fast and accurate long-read alignment with Burrows-Wheeler transform.

Authors:  Heng Li; Richard Durbin
Journal:  Bioinformatics       Date:  2010-01-15       Impact factor: 6.937

10.  Genome-wide association study of PR interval.

Authors:  Arne Pfeufer; Charlotte van Noord; Kristin D Marciante; Dan E Arking; Martin G Larson; Albert Vernon Smith; Kirill V Tarasov; Martina Müller; Nona Sotoodehnia; Moritz F Sinner; Germaine C Verwoert; Man Li; W H Linda Kao; Anna Köttgen; Josef Coresh; Joshua C Bis; Bruce M Psaty; Kenneth Rice; Jerome I Rotter; Fernando Rivadeneira; Albert Hofman; Jan A Kors; Bruno H C Stricker; André G Uitterlinden; Cornelia M van Duijn; Britt M Beckmann; Wiebke Sauter; Christian Gieger; Steven A Lubitz; Christopher Newton-Cheh; Thomas J Wang; Jared W Magnani; Renate B Schnabel; Mina K Chung; John Barnard; Jonathan D Smith; David R Van Wagoner; Ramachandran S Vasan; Thor Aspelund; Gudny Eiriksdottir; Tamara B Harris; Lenore J Launer; Samer S Najjar; Edward Lakatta; David Schlessinger; Manuela Uda; Gonçalo R Abecasis; Bertram Müller-Myhsok; Georg B Ehret; Eric Boerwinkle; Aravinda Chakravarti; Elsayed Z Soliman; Kathryn L Lunetta; Siegfried Perz; H-Erich Wichmann; Thomas Meitinger; Daniel Levy; Vilmundur Gudnason; Patrick T Ellinor; Serena Sanna; Stefan Kääb; Jacqueline C M Witteman; Alvaro Alonso; Emelia J Benjamin; Susan R Heckbert
Journal:  Nat Genet       Date:  2010-01-10       Impact factor: 38.330

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  6 in total

1.  Does Atrial Fibrillation Follow Function? Ion Channel Mutations and Lone Atrial Fibrillation.

Authors:  Sebastian Clauss; Patrick T Ellinor
Journal:  Circ Arrhythm Electrophysiol       Date:  2015-10

2.  Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.

Authors:  Daniel S Evans; Christy L Avery; Mike A Nalls; Guo Li; John Barnard; Erin N Smith; Toshiko Tanaka; Anne M Butler; Sarah G Buxbaum; Alvaro Alonso; Dan E Arking; Gerald S Berenson; Joshua C Bis; Steven Buyske; Cara L Carty; Wei Chen; Mina K Chung; Steven R Cummings; Rajat Deo; Charles B Eaton; Ervin R Fox; Susan R Heckbert; Gerardo Heiss; Lucia A Hindorff; Wen-Chi Hsueh; Aaron Isaacs; Yalda Jamshidi; Kathleen F Kerr; Felix Liu; Yongmei Liu; Kurt K Lohman; Jared W Magnani; Joseph F Maher; Reena Mehra; Yan A Meng; Solomon K Musani; Christopher Newton-Cheh; Kari E North; Bruce M Psaty; Susan Redline; Jerome I Rotter; Renate B Schnabel; Nicholas J Schork; Ralph V Shohet; Andrew B Singleton; Jonathan D Smith; Elsayed Z Soliman; Sathanur R Srinivasan; Herman A Taylor; David R Van Wagoner; James G Wilson; Taylor Young; Zhu-Ming Zhang; Alan B Zonderman; Michele K Evans; Luigi Ferrucci; Sarah S Murray; Gregory J Tranah; Eric A Whitsel; Alex P Reiner; Nona Sotoodehnia
Journal:  Hum Mol Genet       Date:  2016-08-29       Impact factor: 6.150

3.  Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family.

Authors:  Michalina Jagodzińska; Małgorzata Szperl; Joanna Ponińska; Agnieszka Kosiec; Robert Gajda; Piotr Kukla; Elżbieta Katarzyna Biernacka
Journal:  Ann Noninvasive Electrocardiol       Date:  2015-06-24       Impact factor: 1.468

4.  A common variant alters SCN5A-miR-24 interaction and associates with heart failure mortality.

Authors:  Xiaoming Zhang; Jin-Young Yoon; Michael Morley; Jared M McLendon; Kranti A Mapuskar; Rebecca Gutmann; Haider Mehdi; Heather L Bloom; Samuel C Dudley; Patrick T Ellinor; Alaa A Shalaby; Raul Weiss; W H Wilson Tang; Christine S Moravec; Madhurmeet Singh; Anne L Taylor; Clyde W Yancy; Arthur M Feldman; Dennis M McNamara; Kaikobad Irani; Douglas R Spitz; Patrick Breheny; Kenneth B Margulies; Barry London; Ryan L Boudreau
Journal:  J Clin Invest       Date:  2018-02-19       Impact factor: 14.808

Review 5.  Genetics and genomics of arrhythmic risk: current and future strategies to prevent sudden cardiac death.

Authors:  Chiara Scrocco; Connie R Bezzina; Michael J Ackerman; Elijah R Behr
Journal:  Nat Rev Cardiol       Date:  2021-05-24       Impact factor: 32.419

6.  PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.

Authors:  Jessica van Setten; Jennifer A Brody; Yalda Jamshidi; Brenton R Swenson; Anne M Butler; Harry Campbell; Fabiola M Del Greco; Daniel S Evans; Quince Gibson; Daniel F Gudbjartsson; Kathleen F Kerr; Bouwe P Krijthe; Leo-Pekka Lyytikäinen; Christian Müller; Martina Müller-Nurasyid; Ilja M Nolte; Sandosh Padmanabhan; Marylyn D Ritchie; Antonietta Robino; Albert V Smith; Maristella Steri; Toshiko Tanaka; Alexander Teumer; Stella Trompet; Sheila Ulivi; Niek Verweij; Xiaoyan Yin; David O Arnar; Folkert W Asselbergs; Joel S Bader; John Barnard; Josh Bis; Stefan Blankenberg; Eric Boerwinkle; Yuki Bradford; Brendan M Buckley; Mina K Chung; Dana Crawford; Marcel den Hoed; Josh C Denny; Anna F Dominiczak; Georg B Ehret; Mark Eijgelsheim; Patrick T Ellinor; Stephan B Felix; Oscar H Franco; Lude Franke; Tamara B Harris; Hilma Holm; Gandin Ilaria; Annamaria Iorio; Mika Kähönen; Ivana Kolcic; Jan A Kors; Edward G Lakatta; Lenore J Launer; Honghuang Lin; Henry J Lin; Ruth J F Loos; Steven A Lubitz; Peter W Macfarlane; Jared W Magnani; Irene Mateo Leach; Thomas Meitinger; Braxton D Mitchell; Thomas Munzel; George J Papanicolaou; Annette Peters; Arne Pfeufer; Peter P Pramstaller; Olli T Raitakari; Jerome I Rotter; Igor Rudan; Nilesh J Samani; David Schlessinger; Claudia T Silva Aldana; Moritz F Sinner; Jonathan D Smith; Harold Snieder; Elsayed Z Soliman; Timothy D Spector; David J Stott; Konstantin Strauch; Kirill V Tarasov; Unnur Thorsteinsdottir; Andre G Uitterlinden; David R Van Wagoner; Uwe Völker; Henry Völzke; Melanie Waldenberger; Harm Jan Westra; Philipp S Wild; Tanja Zeller; Alvaro Alonso; Christy L Avery; Stefania Bandinelli; Emelia J Benjamin; Francesco Cucca; Marcus Dörr; Luigi Ferrucci; Paolo Gasparini; Vilmundur Gudnason; Caroline Hayward; Susan R Heckbert; Andrew A Hicks; J Wouter Jukema; Stefan Kääb; Terho Lehtimäki; Yongmei Liu; Patricia B Munroe; Afshin Parsa; Ozren Polasek; Bruce M Psaty; Dan M Roden; Renate B Schnabel; Gianfranco Sinagra; Kari Stefansson; Bruno H Stricker; Pim van der Harst; Cornelia M van Duijn; James F Wilson; Sina A Gharib; Paul I W de Bakker; Aaron Isaacs; Dan E Arking; Nona Sotoodehnia
Journal:  Nat Commun       Date:  2018-07-25       Impact factor: 14.919

  6 in total

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