Literature DB >> 23139255

Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts.

Anne M Butler1, Xiaoyan Yin, Daniel S Evans, Michael A Nalls, Erin N Smith, Toshiko Tanaka, Guo Li, Sarah G Buxbaum, Eric A Whitsel, Alvaro Alonso, Dan E Arking, Emelia J Benjamin, Gerald S Berenson, Josh C Bis, Wei Chen, Rajat Deo, Patrick T Ellinor, Susan R Heckbert, Gerardo Heiss, Wen-Chi Hsueh, Brendan J Keating, Kathleen F Kerr, Yun Li, Marian C Limacher, Yongmei Liu, Steven A Lubitz, Kristin D Marciante, Reena Mehra, Yan A Meng, Anne B Newman, Christopher Newton-Cheh, Kari E North, Cameron D Palmer, Bruce M Psaty, P Miguel Quibrera, Susan Redline, Alex P Reiner, Jerome I Rotter, Renate B Schnabel, Nicholas J Schork, Andrew B Singleton, J Gustav Smith, Elsayed Z Soliman, Sathanur R Srinivasan, Zhu-ming Zhang, Alan B Zonderman, Luigi Ferrucci, Sarah S Murray, Michele K Evans, Nona Sotoodehnia, Jared W Magnani, Christy L Avery.   

Abstract

BACKGROUND: The PR interval, as measured by the resting, standard 12-lead ECG, reflects the duration of atrial/atrioventricular nodal depolarization. Substantial evidence exists for a genetic contribution to PR, including genome-wide association studies that have identified common genetic variants at 9 loci influencing PR in populations of European and Asian descent. However, few studies have examined loci associated with PR in African Americans. METHODS AND
RESULTS: We present results from the largest genome-wide association study to date of PR in 13 415 adults of African descent from 10 cohorts. We tested for association between PR (ms) and ≈2.8 million genotyped and imputed single-nucleotide polymorphisms. Imputation was performed using HapMap 2 YRI and CEU panels. Study-specific results, adjusted for global ancestry and clinical correlates of PR, were meta-analyzed using the inverse variance method. Variation in genome-wide test statistic distributions was noted within studies (λ range: 0.9-1.1), although not after genomic control correction was applied to the overall meta-analysis (λ: 1.008). In addition to generalizing previously reported associations with MEIS1, SCN5A, ARHGAP24, CAV1, and TBX5 to African American populations at the genome-wide significance level (P<5.0 × 10(-8)), we also identified a novel locus: ITGA9, located in a region previously implicated in SCN5A expression. The 3p21 region harboring SCN5A also contained 2 additional independent secondary signals influencing PR (P<5.0 × 10(-8)).
CONCLUSIONS: This study demonstrates the ability to map novel loci in African Americans as well as the generalizability of loci associated with PR across populations of African, European, and Asian descent.

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Mesh:

Year:  2012        PMID: 23139255      PMCID: PMC3560365          DOI: 10.1161/CIRCGENETICS.112.963991

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


  42 in total

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Journal:  Circulation       Date:  2007-10-29       Impact factor: 29.690

4.  Practical aspects of imputation-driven meta-analysis of genome-wide association studies.

Authors:  Paul I W de Bakker; Manuel A R Ferreira; Xiaoming Jia; Benjamin M Neale; Soumya Raychaudhuri; Benjamin F Voight
Journal:  Hum Mol Genet       Date:  2008-10-15       Impact factor: 6.150

5.  Ethnic distribution of ECG predictors of atrial fibrillation and its impact on understanding the ethnic distribution of ischemic stroke in the Atherosclerosis Risk in Communities (ARIC) study.

Authors:  Elsayed Z Soliman; Ronald J Prineas; L Douglas Case; Zhu-ming Zhang; David C Goff
Journal:  Stroke       Date:  2009-02-12       Impact factor: 7.914

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

Review 7.  Atrial fibrillation and congestive heart failure.

Authors:  Denis Roy; Mario Talajic; Marc Dubuc; Bernard Thibault; Peter Guerra; Laurent Macle; Paul Khairy
Journal:  Curr Opin Cardiol       Date:  2009-01       Impact factor: 2.161

Review 8.  Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations.

Authors:  Carol Ann Remme; Arthur A M Wilde; Connie R Bezzina
Journal:  Trends Cardiovasc Med       Date:  2008-04       Impact factor: 6.677

9.  Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

Authors:  Arne Pfeufer; Serena Sanna; Dan E Arking; Martina Müller; Vesela Gateva; Christian Fuchsberger; Georg B Ehret; Marco Orrú; Cristian Pattaro; Anna Köttgen; Siegfried Perz; Gianluca Usala; Maja Barbalic; Man Li; Benno Pütz; Angelo Scuteri; Ronald J Prineas; Moritz F Sinner; Christian Gieger; Samer S Najjar; W H Linda Kao; Thomas W Mühleisen; Mariano Dei; Christine Happle; Stefan Möhlenkamp; Laura Crisponi; Raimund Erbel; Karl-Heinz Jöckel; Silvia Naitza; Gerhard Steinbeck; Fabio Marroni; Andrew A Hicks; Edward Lakatta; Bertram Müller-Myhsok; Peter P Pramstaller; H-Erich Wichmann; David Schlessinger; Eric Boerwinkle; Thomas Meitinger; Manuela Uda; Josef Coresh; Stefan Kääb; Gonçalo R Abecasis; Aravinda Chakravarti
Journal:  Nat Genet       Date:  2009-03-22       Impact factor: 38.330

10.  Common variants at ten loci influence QT interval duration in the QTGEN Study.

Authors:  Christopher Newton-Cheh; Mark Eijgelsheim; Kenneth M Rice; Paul I W de Bakker; Xiaoyan Yin; Karol Estrada; Joshua C Bis; Kristin Marciante; Fernando Rivadeneira; Peter A Noseworthy; Nona Sotoodehnia; Nicholas L Smith; Jerome I Rotter; Jan A Kors; Jacqueline C M Witteman; Albert Hofman; Susan R Heckbert; Christopher J O'Donnell; André G Uitterlinden; Bruce M Psaty; Thomas Lumley; Martin G Larson; Bruno H Ch Stricker
Journal:  Nat Genet       Date:  2009-03-22       Impact factor: 38.330

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  30 in total

Review 1.  First-degree AV block-an entirely benign finding or a potentially curable cause of cardiac disease?

Authors:  Fredrik Holmqvist; James P Daubert
Journal:  Ann Noninvasive Electrocardiol       Date:  2013-05       Impact factor: 1.468

2.  Genetic determinants of P wave duration and PR segment.

Authors:  Niek Verweij; Irene Mateo Leach; Malou van den Boogaard; Dirk J van Veldhuisen; Vincent M Christoffels; Hans L Hillege; Wiek H van Gilst; Phil Barnett; Rudolf A de Boer; Pim van der Harst
Journal:  Circ Cardiovasc Genet       Date:  2014-05-21

3.  Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation.

Authors:  Mariam B Seifert; Morten S Olesen; Ingrid E Christophersen; Jonas B Nielsen; Jonas Carlson; Fredrik Holmqvist; Arnljot Tveit; Stig Haunsø; Jesper H Svendsen; Pyotr G Platonov
Journal:  Ann Noninvasive Electrocardiol       Date:  2019-06-01       Impact factor: 1.468

4.  Lack of association between rs3807989 in cav1 and atrial fibrillation.

Authors:  Guocao Li; Rongfeng Zhang; Lianjun Gao; Shulong Zhang; Yingxue Dong; Xiaomeng Yin; Dong Chang; Yanzong Yang; Yunlong Xia
Journal:  Int J Clin Exp Pathol       Date:  2014-06-15

5.  Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population.

Authors:  Qingyi Wei; Dianke Yu; Mingbo Liu; Mengyun Wang; Miaoqing Zhao; Ming Liu; Weihua Jia; Hongxia Ma; Jugao Fang; Wei Xu; Kexing Chen; Zhengang Xu; Jialing Wang; Linli Tian; Hua Yuan; Jiang Chang; Zhibin Hu; Lixun Wei; Ying Huang; Yaling Han; Jie Liu; Demin Han; Hongbing Shen; Shiming Yang; Hong Zheng; Qinghai Ji; Duanshu Li; Wen Tan; Chen Wu; Dongxin Lin
Journal:  Nat Genet       Date:  2014-09-07       Impact factor: 38.330

6.  GAREM1 regulates the PR interval on electrocardiograms.

Authors:  Hye Ok Kim; Ji Eun Lim; Myung Jun Kim; Ji-One Kang; Sung-Moon Kim; Jeong Min Nam; Jihoon Tak; Hiroaki Konishi; Tasuku Nishino; In Song Koh; Young-Ho Jin; Hyung Hwan Baik; Jin-Bae Kim; Mi Kyung Kim; Bo Youl Choi; Sang-Hak Lee; Yangsoo Jang; Jinho Shin; Bermseok Oh
Journal:  J Hum Genet       Date:  2017-12-22       Impact factor: 3.172

7.  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

8.  Functional characterization of SCN10A variants in several cases of sudden unexplained death.

Authors:  Ivan Gando; Nori Williams; Glenn I Fishman; Barbara A Sampson; Yingying Tang; William A Coetzee
Journal:  Forensic Sci Int       Date:  2019-05-29       Impact factor: 2.395

9.  Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF).

Authors:  Sanghamitra Mohanty; Amelia W Hall; Prasant Mohanty; Sameer Prakash; Chintan Trivedi; Luigi Di Biase; Pasquale Santangeli; Rong Bai; J David Burkhardt; G Joseph Gallinghouse; Rodney Horton; Javier E Sanchez; Patrick M Hranitzky; Amin Al-Ahmad; Vishwanath R Iyer; Andrea Natale
Journal:  J Interv Card Electrophysiol       Date:  2016-01       Impact factor: 1.900

10.  Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.

Authors:  Honghuang Lin; Jessica van Setten; Albert V Smith; Nathan A Bihlmeyer; Helen R Warren; Jennifer A Brody; Farid Radmanesh; Leanne Hall; Niels Grarup; Martina Müller-Nurasyid; Thibaud Boutin; Niek Verweij; Henry J Lin; Ruifang Li-Gao; Marten E van den Berg; Jonathan Marten; Stefan Weiss; Bram P Prins; Jeffrey Haessler; Leo-Pekka Lyytikäinen; Hao Mei; Tamara B Harris; Lenore J Launer; Man Li; Alvaro Alonso; Elsayed Z Soliman; John M Connell; Paul L Huang; Lu-Chen Weng; Heather S Jameson; William Hucker; Alan Hanley; Nathan R Tucker; Yii-Der Ida Chen; Joshua C Bis; Kenneth M Rice; Colleen M Sitlani; Jan A Kors; Zhijun Xie; Chengping Wen; Jared W Magnani; Christopher P Nelson; Jørgen K Kanters; Moritz F Sinner; Konstantin Strauch; Annette Peters; Melanie Waldenberger; Thomas Meitinger; Jette Bork-Jensen; Oluf Pedersen; Allan Linneberg; Igor Rudan; Rudolf A de Boer; Peter van der Meer; Jie Yao; Xiuqing Guo; Kent D Taylor; Nona Sotoodehnia; Jerome I Rotter; Dennis O Mook-Kanamori; Stella Trompet; Fernando Rivadeneira; André Uitterlinden; Mark Eijgelsheim; Sandosh Padmanabhan; Blair H Smith; Henry Völzke; Stephan B Felix; Georg Homuth; Uwe Völker; Massimo Mangino; Timothy D Spector; Michiel L Bots; Marco Perez; Mika Kähönen; Olli T Raitakari; Vilmundur Gudnason; Dan E Arking; Patricia B Munroe; Bruce M Psaty; Cornelia M van Duijn; Emelia J Benjamin; Jonathan Rosand; Nilesh J Samani; Torben Hansen; Stefan Kääb; Ozren Polasek; Pim van der Harst; Susan R Heckbert; J Wouter Jukema; Bruno H Stricker; Caroline Hayward; Marcus Dörr; Yalda Jamshidi; Folkert W Asselbergs; Charles Kooperberg; Terho Lehtimäki; James G Wilson; Patrick T Ellinor; Steven A Lubitz; Aaron Isaacs
Journal:  Circ Genom Precis Med       Date:  2018-05
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