Literature DB >> 20215044

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

Kimmo Porthan1, Annukka Marjamaa, Matti Viitasalo, Heikki Väänänen, Antti Jula, Lauri Toivonen, Markku S Nieminen, Christopher Newton-Cheh, Veikko Salomaa, Kimmo Kontula, Lasse Oikarinen.   

Abstract

BACKGROUND: Single-nucleotide polymorphisms (SNPs) in genes encoding cardiac ion channels and nitric oxide synthase-1 adaptor protein (NOS1AP) are associated with electrocardiographic (ECG) QT-interval duration, but the association of these SNPs with new, prognostically important ECG measures of ventricular repolarization is unknown.
OBJECTIVE: The purpose of this study was to examine the relationship of SNPs to ECG T-wave peak to T-wave end (TPE) interval and T-wave morphology parameters.
METHODS: We studied 5,890 adults attending the Health 2000 Study, a Finnish epidemiologic survey. TPE interval and four T-wave morphology parameters were measured from digital 12-lead ECGs and related to the seven SNPs showing a phenotypic effect on QT-interval duration in the Health 2000 Study population.
RESULTS: In multivariable analyses, the KCNH2 K897T minor allele was associated with a 1.2-ms TPE-interval shortening (P = .00005) and the KCNH2 intronic rs3807375 minor allele was associated with a 0.8-ms TPE-interval prolongation (P = .001), whereas the KCNE1 D85N variant had no TPE-interval effect (P = .20). NOS1AP minor alleles (rs2880058, rs4657139, rs10918594, rs10494366) were associated with a shorter TPE interval (effects from 0.5 to 0.8 ms, P from .032 to .002), which resulted from their stronger effects on QT(peak) than QT(end) interval. None of the SNPs showed a consistent association with T-wave morphology parameters.
CONCLUSION: KCNH2 K897T and rs3807375 as well as the four studied NOS1AP variants have modest effects on ECG TPE interval but are not related to T-wave morphology measures. The previously observed prognostic value of T-wave morphology parameters likely is not based on these SNPs. Copyright 2010 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20215044      PMCID: PMC2904845          DOI: 10.1016/j.hrthm.2010.03.002

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  33 in total

1.  Reproducibility of computerized measurements of QT interval from multiple leads at rest and during exercise.

Authors:  Anna-Mari Hekkala; Heikki Väänänen; Heikki Swan; Lasse Oikarinen; Matti Viitasalo; Lauri Toivonen
Journal:  Ann Noninvasive Electrocardiol       Date:  2006-10       Impact factor: 1.468

2.  CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart.

Authors:  Kuan-Cheng Chang; Andreas S Barth; Tetsuo Sasano; Eddy Kizana; Yuji Kashiwakura; Yiqiang Zhang; D Brian Foster; Eduardo Marbán
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-12       Impact factor: 11.205

3.  Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.

Authors:  W H Linda Kao; Dan E Arking; Wendy Post; Thomas D Rea; Nona Sotoodehnia; Ronald J Prineas; Bryan Bishe; Betty Q Doan; Eric Boerwinkle; Bruce M Psaty; Gordon F Tomaselli; Josef Coresh; David S Siscovick; Eduardo Marbán; Peter M Spooner; Gregory L Burke; Aravinda Chakravarti
Journal:  Circulation       Date:  2009-02-09       Impact factor: 29.690

Review 4.  Genetic determinants of sudden cardiac death.

Authors:  Peter A Noseworthy; Christopher Newton-Cheh
Journal:  Circulation       Date:  2008-10-28       Impact factor: 29.690

5.  New descriptors of T-wave morphology are independent of heart rate.

Authors:  Mads P Andersen; Joel Q Xue; Claus Graff; Jørgen K Kanters; Egon Toft; Johannes J Struijk
Journal:  J Electrocardiol       Date:  2008-09-19       Impact factor: 1.438

Review 6.  Cellular basis for the repolarization waves of the ECG.

Authors:  Charles Antzelevitch
Journal:  Ann N Y Acad Sci       Date:  2006-10       Impact factor: 5.691

7.  Relationship of electrocardiographic repolarization measures to echocardiographic left ventricular mass in men with hypertension.

Authors:  Kimmo Porthan; Juha Virolainen; Timo P Hiltunen; Matti Viitasalo; Heikki Väänänen; Juhani Dabek; Tuula Hannila-Handelberg; Lauri Toivonen; Markku S Nieminen; Kimmo Kontula; Lasse Oikarinen
Journal:  J Hypertens       Date:  2007-09       Impact factor: 4.844

8.  The human ERG1 channel polymorphism, K897T, creates a phosphorylation site that inhibits channel activity.

Authors:  Saverio Gentile; Negin Martin; Erica Scappini; Jason Williams; Christian Erxleben; David L Armstrong
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-12       Impact factor: 11.205

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.  Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.

Authors:  Xianqin Zhang; Shenghan Chen; Li Zhang; Mugen Liu; Sharon Redfearn; Randall M Bryant; Carlos Oberti; G Michael Vincent; Qing K Wang
Journal:  BMC Med Genet       Date:  2008-09-23       Impact factor: 2.103

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  12 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.  Functional differences between junctional and extrajunctional adrenergic receptor activation in mammalian ventricle.

Authors:  Olujimi A Ajijola; Marmar Vaseghi; Wei Zhou; Kentaro Yamakawa; Peyman Benharash; Joseph Hadaya; Robert L Lux; Aman Mahajan; Kalyanam Shivkumar
Journal:  Am J Physiol Heart Circ Physiol       Date:  2012-12-15       Impact factor: 4.733

Review 3.  Clinical and genetic determinants of torsade de pointes risk.

Authors:  Andrew J Sauer; Christopher Newton-Cheh
Journal:  Circulation       Date:  2012-04-03       Impact factor: 29.690

4.  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

5.  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

6.  A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.

Authors:  Stefan Kääb; Dana C Crawford; Moritz F Sinner; Elijah R Behr; Prince J Kannankeril; Arthur A M Wilde; Connie R Bezzina; Eric Schulze-Bahr; Pascale Guicheney; Nanette H Bishopric; Robert J Myerburg; Jean-Jacques Schott; Arne Pfeufer; Britt-Maria Beckmann; Eimo Martens; Taifang Zhang; Birgit Stallmeyer; Sven Zumhagen; Isabelle Denjoy; Abdennasser Bardai; Isabelle C Van Gelder; Yalda Jamshidi; Chrysoula Dalageorgou; Vanessa Marshall; Steve Jeffery; Saad Shakir; A John Camm; Gerhard Steinbeck; Siegfried Perz; Peter Lichtner; Thomas Meitinger; Annette Peters; H-Erich Wichmann; Christiana Ingram; Yuki Bradford; Shannon Carter; Kris Norris; Marylyn D Ritchie; Alfred L George; Dan M Roden
Journal:  Circ Cardiovasc Genet       Date:  2011-11-18

Review 7.  KCNE genetics and pharmacogenomics in cardiac arrhythmias: much ado about nothing?

Authors:  Geoffrey W Abbott
Journal:  Expert Rev Clin Pharmacol       Date:  2013-01       Impact factor: 5.045

8.  Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.

Authors:  Jonathan M Kocarnik; Melissa Richard; Misa Graff; Jeffrey Haessler; Stephanie Bien; Chris Carlson; Cara L Carty; Alexander P Reiner; Christy L Avery; Christie M Ballantyne; Andrea Z LaCroix; Themistocles L Assimes; Maja Barbalic; Nathan Pankratz; Weihong Tang; Ran Tao; Dongquan Chen; Gregory A Talavera; Martha L Daviglus; Diana A Chirinos-Medina; Rocio Pereira; Katie Nishimura; Petra Bužková; Lyle G Best; José Luis Ambite; Iona Cheng; Dana C Crawford; Lucia A Hindorff; Myriam Fornage; Gerardo Heiss; Kari E North; Christopher A Haiman; Ulrike Peters; Loic Le Marchand; Charles Kooperberg
Journal:  Hum Mol Genet       Date:  2018-08-15       Impact factor: 6.150

Review 9.  KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulation.

Authors:  Geoffrey W Abbott
Journal:  Gene       Date:  2015-09-26       Impact factor: 3.688

10.  The Relationship between Angiotensin-II Type 1 Receptor Gene Polymorphism and Repolarization Parameters after a First Anterior Acute Myocardial Infarction.

Authors:  Onder Ozturk; Unal Ozturk; Sebnem Nergiz; M Zulkif Karahan
Journal:  Korean Circ J       Date:  2016-11-01       Impact factor: 3.243

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