Literature DB >> 23534349

Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.

Janina M Jeff1, Marylyn D Ritchie, Joshua C Denny, Abel N Kho, Andrea H Ramirez, David Crosslin, Loren Armstrong, Melissa A Basford, Wendy A Wolf, Jennifer A Pacheco, Rex L Chisholm, Dan M Roden, M Geoffrey Hayes, Dana C Crawford.   

Abstract

Electrocardiographic (ECG) measurements vary by ancestry. Genome-wide association studies (GWAS) have identified loci that contribute to ECG measurements; however, most are performed in Europeans collected from population-based cohorts or surveys. The strongest associations reported are in NOS1AP with QT interval and SCN10A with PR and QRS durations. The extent to which these associations can be generalized to African Americans has yet to be determined. Using electronic medical records, PR and QT intervals, QRS duration, and heart rate were determined in 455 African Americans as part of the Vanderbilt Genome-Electronic Records Project and Northwestern University NUgene Project. We tested for an association between these ECG traits and >930K SNPs. We identified a total 36 novel associations with PR interval, QRS duration, QT interval, and heart rate at p < 1.0 × 10(-6). Using published GWAS data, we compared our results with those previously identified in other populations. Five associations originally identified in other populations generalized with respect to statistical significance and direction of effect. A total of 43 associations have a consistent direction of effect with European and/or Asian populations. This work provides a catalogue of generalized versus nongeneralized associations, a necessary step in prioritizing GWAS-identified regions for further fine-mapping in diverse populations.
© 2013 John Wiley & Sons Ltd/University College London.

Entities:  

Keywords:  African Americans; Electrocardiography; GWAS; electronic medical records; generalization

Mesh:

Year:  2013        PMID: 23534349      PMCID: PMC3743946          DOI: 10.1111/ahg.12023

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  41 in total

1.  Modulators of normal electrocardiographic intervals identified in a large electronic medical record.

Authors:  Andrea H Ramirez; Jonathan S Schildcrout; Dana L Blakemore; Dan R Masys; Jill M Pulley; Melissa A Basford; Dan M Roden; Joshua C Denny
Journal:  Heart Rhythm       Date:  2010-10-29       Impact factor: 6.343

2.  Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.

Authors:  Solveig Gretarsdottir; Annette F Baas; Gudmar Thorleifsson; Hilma Holm; Martin den Heijer; Jean-Paul P M de Vries; Steef E Kranendonk; Clark J A M Zeebregts; Steven M van Sterkenburg; Robert H Geelkerken; Andre M van Rij; Michael J A Williams; Albert P M Boll; Jelena P Kostic; Adalbjorg Jonasdottir; Aslaug Jonasdottir; G Bragi Walters; Gisli Masson; Patrick Sulem; Jona Saemundsdottir; Magali Mouy; Kristinn P Magnusson; Gerard Tromp; James R Elmore; Natzi Sakalihasan; Raymond Limet; Jean-Olivier Defraigne; Robert E Ferrell; Antti Ronkainen; Ynte M Ruigrok; Cisca Wijmenga; Diederick E Grobbee; Svati H Shah; Christopher B Granger; Arshed A Quyyumi; Viola Vaccarino; Riyaz S Patel; A Maziar Zafari; Allan I Levey; Harland Austin; Domenico Girelli; Pier Franco Pignatti; Oliviero Olivieri; Nicola Martinelli; Giovanni Malerba; Elisabetta Trabetti; Lewis C Becker; Diane M Becker; Muredach P Reilly; Daniel J Rader; Thomas Mueller; Benjamin Dieplinger; Meinhard Haltmayer; Sigitas Urbonavicius; Bengt Lindblad; Anders Gottsäter; Eleonora Gaetani; Roberto Pola; Philip Wells; Marc Rodger; Melissa Forgie; Nicole Langlois; Javier Corral; Vicente Vicente; Jordi Fontcuberta; Francisco España; Niels Grarup; Torben Jørgensen; Daniel R Witte; Torben Hansen; Oluf Pedersen; Katja K Aben; Jacqueline de Graaf; Suzanne Holewijn; Lasse Folkersen; Anders Franco-Cereceda; Per Eriksson; David A Collier; Hreinn Stefansson; Valgerdur Steinthorsdottir; Thorunn Rafnar; Einar M Valdimarsson; Hulda B Magnadottir; Sigurlaug Sveinbjornsdottir; Isleifur Olafsson; Magnus Karl Magnusson; Robert Palmason; Vilhelmina Haraldsdottir; Karl Andersen; Pall T Onundarson; Gudmundur Thorgeirsson; Lambertus A Kiemeney; Janet T Powell; David J Carey; Helena Kuivaniemi; Jes S Lindholt; Gregory T Jones; Augustine Kong; Jan D Blankensteijn; Stefan E Matthiasson; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Nat Genet       Date:  2010-07-11       Impact factor: 38.330

3.  Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.

Authors:  David R Crosslin; Andrew McDavid; Noah Weston; Sarah C Nelson; Xiuwen Zheng; Eugene Hart; Mariza de Andrade; Iftikhar J Kullo; Catherine A McCarty; Kimberly F Doheny; Elizabeth Pugh; Abel Kho; M Geoffrey Hayes; Stephanie Pretel; Alexander Saip; Marylyn D Ritchie; Dana C Crawford; Paul K Crane; Katherine Newton; Rongling Li; Daniel B Mirel; Andrew Crenshaw; Eric B Larson; Chris S Carlson; Gail P Jarvik
Journal:  Hum Genet       Date:  2011-10-30       Impact factor: 4.132

Review 4.  Genome-wide association studies in diverse populations.

Authors:  Noah A Rosenberg; Lucy Huang; Ethan M Jewett; Zachary A Szpiech; Ivana Jankovic; Michael Boehnke
Journal:  Nat Rev Genet       Date:  2010-05       Impact factor: 53.242

5.  Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.

Authors:  Rebecca L Zuvich; Loren L Armstrong; Suzette J Bielinski; Yuki Bradford; Christopher S Carlson; Dana C Crawford; Andrew T Crenshaw; Mariza de Andrade; Kimberly F Doheny; Jonathan L Haines; M Geoffrey Hayes; Gail P Jarvik; Lan Jiang; Iftikhar J Kullo; Rongling Li; Hua Ling; Teri A Manolio; Martha E Matsumoto; Catherine A McCarty; Andrew N McDavid; Daniel B Mirel; Lana M Olson; Justin E Paschall; Elizabeth W Pugh; Luke V Rasmussen; Laura J Rasmussen-Torvik; Stephen D Turner; Russell A Wilke; Marylyn D Ritchie
Journal:  Genet Epidemiol       Date:  2011-12       Impact factor: 2.135

6.  Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae.

Authors:  J Gustav Smith; Jennifer K Lowe; Sirisha Kovvali; Julian B Maller; Jacqueline Salit; Mark J Daly; Markus Stoffel; David M Altshuler; Jeffrey M Friedman; Jan L Breslow; Christopher Newton-Cheh
Journal:  Heart Rhythm       Date:  2009-02-15       Impact factor: 6.343

7.  Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.

Authors:  Hua Zhong; Ross L Prentice
Journal:  Genet Epidemiol       Date:  2010-01       Impact factor: 2.135

8.  Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

Authors:  Stephen D Turner; Richard L Berg; James G Linneman; Peggy L Peissig; Dana C Crawford; Joshua C Denny; Dan M Roden; Catherine A McCarty; Marylyn D Ritchie; Russell A Wilke
Journal:  PLoS One       Date:  2011-05-11       Impact factor: 3.240

9.  Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis.

Authors:  Sarah A Pendergrass; Scott M Dudek; Dana C Crawford; Marylyn D Ritchie
Journal:  BioData Min       Date:  2010-12-16       Impact factor: 2.522

10.  Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip.

Authors:  Chris C A Spencer; Zhan Su; Peter Donnelly; Jonathan Marchini
Journal:  PLoS Genet       Date:  2009-05-15       Impact factor: 5.917

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  21 in total

1.  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
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2.  An endophenotype approach to the genetics of alcohol dependence: a genome wide association study of fast beta EEG in families of African ancestry.

Authors:  J L Meyers; J Zhang; J C Wang; J Su; S I Kuo; M Kapoor; L Wetherill; S Bertelsen; D Lai; J E Salvatore; C Kamarajan; D Chorlian; A Agrawal; L Almasy; L Bauer; K K Bucholz; G Chan; V Hesselbrock; L Koganti; J Kramer; S Kuperman; N Manz; A Pandey; M Seay; D Scott; R E Taylor; D M Dick; H J Edenberg; A Goate; T Foroud; B Porjesz
Journal:  Mol Psychiatry       Date:  2017-01-10       Impact factor: 15.992

3.  Novel Therapeutic Strategies for the Management of Ventricular Arrhythmias Associated with the Brugada Syndrome.

Authors:  Bence Patocskai; Charles Antzelevitch
Journal:  Expert Opin Orphan Drugs       Date:  2015-05-13       Impact factor: 0.694

Review 4.  Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.

Authors:  Emmanuel Peprah; Huichun Xu; Fasil Tekola-Ayele; Charmaine D Royal
Journal:  Public Health Genomics       Date:  2014-11-26       Impact factor: 2.000

5.  Replication of SCN5A Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies.

Authors:  Janina M Jeff; Kristin Brown-Gentry; Robert Goodloe; Marylyn D Ritchie; Joshua C Denny; Abel N Kho; Loren L Armstrong; Bob McClellan; Ping Mayo; Melissa Allen; Hailing Jin; Niloufar B Gillani; Nathalie Schnetz-Boutaud; Holli H Dilks; Melissa A Basford; Jennifer A Pacheco; Gail P Jarvik; Rex L Chisholm; Dan M Roden; M Geoffrey Hayes; Dana C Crawford
Journal:  Evol Comput Mach Learn Data Min Bioinform       Date:  2014

6.  Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome.

Authors:  Dan Hu; Hector Barajas-Martínez; Ryan Pfeiffer; Fabio Dezi; Jenna Pfeiffer; Tapan Buch; Matthew J Betzenhauser; Luiz Belardinelli; Kristopher M Kahlig; Sridharan Rajamani; Harry J DeAntonio; Robert J Myerburg; Hiroyuki Ito; Pramod Deshmukh; Mark Marieb; Gi-Byoung Nam; Atul Bhatia; Can Hasdemir; Michel Haïssaguerre; Christian Veltmann; Rainer Schimpf; Martin Borggrefe; Sami Viskin; Charles Antzelevitch
Journal:  J Am Coll Cardiol       Date:  2014-07-08       Impact factor: 24.094

Review 7.  The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology.

Authors:  Christiaan C Veerman; Arthur A M Wilde; Elisabeth M Lodder
Journal:  Gene       Date:  2015-09-08       Impact factor: 3.688

Review 8.  Brugada Syndrome: Clinical, Genetic, Molecular, Cellular, and Ionic Aspects.

Authors:  Charles Antzelevitch; Bence Patocskai
Journal:  Curr Probl Cardiol       Date:  2015-06-11       Impact factor: 5.200

9.  Secondary use of clinical data: the Vanderbilt approach.

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10.  The anatomical distribution of genetic associations.

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Journal:  Nucleic Acids Res       Date:  2015-11-19       Impact factor: 16.971

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