Literature DB >> 19019189

Common candidate gene variants are associated with QT interval duration in the general population.

A Marjamaa1, C Newton-Cheh, K Porthan, A Reunanen, P Lahermo, H Väänänen, A Jula, H Karanko, H Swan, L Toivonen, M S Nieminen, M Viitasalo, L Peltonen, L Oikarinen, A Palotie, K Kontula, V Salomaa.   

Abstract

OBJECTIVES: QT interval prolongation is associated with increased risk of sudden cardiac death at the population level. As 30-40% of the QT-interval variability is heritable, we tested the association of common LQTS and NOS1AP gene variants with QT interval in a Finnish population-based sample.
METHODS: We genotyped 12 common LQTS and NOS1AP genetic variants in Health 2000, an epidemiological sample of 5043 Finnish individuals, using Sequenom MALDI-TOF mass spectrometry. ECG parameters were measured from digital 12-lead ECGs and QT intervals were adjusted for age, gender and heart rate with a nomogram (Nc) method derived from the present study population.
RESULTS: The KCNE1 D85N minor allele (frequency 1.4%) was associated with a 10.5 ms (SE 1.6) or 0.57 SD prolongation of the adjusted QT(Nc) interval (P=3.6 x 10(-11)) in gender-pooled analysis. In agreement with previous studies, we replicated the association with QT(Nc) interval with minor alleles of KCNH2 intronic SNP rs3807375 [1.6 ms (SE 0.4) or 0.08 SD, P=4.7 x 10(-5)], KCNH2 K897T [-2.6 ms (SE 0.5) or -0.14 SD, P=2.1 x 10(-7)] and NOSA1P variants including rs2880058 [4.0 ms (SE 0.4) or 0.22 SD, P=3.2 x 10(-24)] under additive models.
CONCLUSIONS: We demonstrate that each additional copy of the KCNE1 D85N minor allele is associated with a considerable 10.5 ms prolongation of the age-, gender- and heart rate-adjusted QT interval and could thus modulate repolarization-related arrhythmia susceptibility at the population level. In addition, we robustly confirm the previous findings that three independent KCNH2 and NOSA1P variants are associated with adjusted QT interval.

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Year:  2009        PMID: 19019189      PMCID: PMC2668713          DOI: 10.1111/j.1365-2796.2008.02026.x

Source DB:  PubMed          Journal:  J Intern Med        ISSN: 0954-6820            Impact factor:   8.989


  50 in total

1.  QT interval as a cardiac risk factor in a middle aged population.

Authors:  J Karjalainen; A Reunanen; P Ristola; M Viitasalo
Journal:  Heart       Date:  1997-06       Impact factor: 5.994

2.  The normal unipolar precordial and limb lead electrocardiogram.

Authors:  M SOKOLOW; R D FREIDLANDER
Journal:  Am Heart J       Date:  1949-11       Impact factor: 4.749

3.  MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.

Authors:  G W Abbott; F Sesti; I Splawski; M E Buck; M H Lehmann; K W Timothy; M T Keating; S A Goldstein
Journal:  Cell       Date:  1999-04-16       Impact factor: 41.582

4.  Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome.

Authors:  F Tesson; C Donger; I Denjoy; M Berthet; M Bennaceur; C Petit; P Coumel; K Schwarts; P Guicheney
Journal:  J Mol Cell Cardiol       Date:  1996-09       Impact factor: 5.000

5.  Polymorphism of the gene encoding a human minimal potassium ion channel (minK).

Authors:  L P Lai; C L Deng; A J Moss; R S Kass; C S Liang
Journal:  Gene       Date:  1994-12-30       Impact factor: 3.688

6.  Role of a KCNH2 polymorphism (R1047 L) in dofetilide-induced Torsades de Pointes.

Authors:  Zhuoqian Sun; Patrice M Milos; John F Thompson; David B Lloyd; Amy Mank-Seymour; Jodi Richmond; Jason S Cordes; Jun Zhou
Journal:  J Mol Cell Cardiol       Date:  2004-11       Impact factor: 5.000

7.  Magnetocardiographic QT interval dispersion in postmyocardial infarction patients with sustained ventricular tachycardia: validation of automated QT measurements.

Authors:  L Oikarinen; M Paavola; J Montonen; M Viitasalo; M Mäkijärvi; L Toivonen; T Katila
Journal:  Pacing Clin Electrophysiol       Date:  1998-10       Impact factor: 1.976

8.  Electrocardiographic detection of left ventricular hypertrophy by the simple QRS voltage-duration product.

Authors:  T J Molloy; P M Okin; R B Devereux; P Kligfield
Journal:  J Am Coll Cardiol       Date:  1992-11-01       Impact factor: 24.094

9.  Common genetic variation in KCNH2 is associated with QT interval duration: the Framingham Heart Study.

Authors:  Christopher Newton-Cheh; Chao-Yu Guo; Martin G Larson; Stacy L Musone; Aarti Surti; Amy L Camargo; Jared A Drake; Emelia J Benjamin; Daniel Levy; Ralph B D'Agostino; Joel N Hirschhorn; Christopher J O'donnell
Journal:  Circulation       Date:  2007-08-20       Impact factor: 29.690

10.  Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry.

Authors:  E H Locati; W Zareba; A J Moss; P J Schwartz; G M Vincent; M H Lehmann; J A Towbin; S G Priori; C Napolitano; J L Robinson; M Andrews; K Timothy; W J Hall
Journal:  Circulation       Date:  1998-06-09       Impact factor: 29.690

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  33 in total

1.  Common genetic variants, QT interval, and sudden cardiac death in a Finnish population-based study.

Authors:  Peter A Noseworthy; Aki S Havulinna; Kimmo Porthan; Annukka M Lahtinen; Antti Jula; Pekka J Karhunen; Markus Perola; Lasse Oikarinen; Kimmo K Kontula; Veikko Salomaa; Christopher Newton-Cheh
Journal:  Circ Cardiovasc Genet       Date:  2011-04-21

2.  Trafficking of the human ether-a-go-go-related gene (hERG) potassium channel is regulated by the ubiquitin ligase rififylin (RFFL).

Authors:  Karim Roder; Anatoli Kabakov; Karni S Moshal; Kevin R Murphy; An Xie; Samuel Dudley; Nilüfer N Turan; Yichun Lu; Calum A MacRae; Gideon Koren
Journal:  J Biol Chem       Date:  2018-11-06       Impact factor: 5.157

3.  Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant.

Authors:  Conor M Lane; John R Giudicessi; Dan Ye; David J Tester; Ram K Rohatgi; J Martijn Bos; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2018-04-03       Impact factor: 6.343

4.  Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.

Authors:  Annukka M Lahtinen; Aki S Havulinna; Peter A Noseworthy; Antti Jula; Pekka J Karhunen; Markus Perola; Christopher Newton-Cheh; Veikko Salomaa; Kimmo Kontula
Journal:  Ann Med       Date:  2013-05-08       Impact factor: 4.709

5.  The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.

Authors:  Iliana Tzimas; Jana-Christin Zingraf; Thomas Bajanowski; Micaela Poetsch
Journal:  Int J Legal Med       Date:  2016-07-26       Impact factor: 2.686

6.  A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.

Authors:  Annukka Marjamaa; Lasse Oikarinen; Kimmo Porthan; Samuli Ripatti; Gina Peloso; Peter A Noseworthy; Matti Viitasalo; Markku S Nieminen; Lauri Toivonen; Kimmo Kontula; Leena Peltonen; Aki S Havulinna; Antti Jula; Christopher J O'Donnell; Christopher Newton-Cheh; Markus Perola; Veikko Salomaa
Journal:  Heart Rhythm       Date:  2012-02-15       Impact factor: 6.343

7.  Relationship of common candidate gene variants to electrocardiographic T-wave peak to T-wave end interval and T-wave morphology parameters.

Authors:  Kimmo Porthan; Annukka Marjamaa; Matti Viitasalo; Heikki Väänänen; Antti Jula; Lauri Toivonen; Markku S Nieminen; Christopher Newton-Cheh; Veikko Salomaa; Kimmo Kontula; Lasse Oikarinen
Journal:  Heart Rhythm       Date:  2010-03-04       Impact factor: 6.343

8.  Non optical semi-conductor next generation sequencing of the main cardiac QT-interval duration genes in pooled DNA samples.

Authors:  Juan Gómez; Julian R Reguero; César Morís; Victoria Alvarez; Eliecer Coto
Journal:  J Cardiovasc Transl Res       Date:  2013-11-05       Impact factor: 4.132

9.  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

10.  Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

Authors:  Ilja M Nolte; Chris Wallace; Stephen J Newhouse; Daryl Waggott; Jingyuan Fu; Nicole Soranzo; Rhian Gwilliam; Panos Deloukas; Irina Savelieva; Dongling Zheng; Chrysoula Dalageorgou; Martin Farrall; Nilesh J Samani; John Connell; Morris Brown; Anna Dominiczak; Mark Lathrop; Eleftheria Zeggini; Louise V Wain; Christopher Newton-Cheh; Mark Eijgelsheim; Kenneth Rice; Paul I W de Bakker; Arne Pfeufer; Serena Sanna; Dan E Arking; Folkert W Asselbergs; Tim D Spector; Nicholas D Carter; Steve Jeffery; Martin Tobin; Mark Caulfield; Harold Snieder; Andrew D Paterson; Patricia B Munroe; Yalda Jamshidi
Journal:  PLoS One       Date:  2009-07-09       Impact factor: 3.240

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