Literature DB >> 18674739

Effect of common KCNE1 and SCN5A ion channel gene variants on T-wave alternans, a marker of cardiac repolarization, during clinical exercise stress test: the Finnish Cardiovascular Study.

Jenni Koskela1, Mika Kähönen, Meng Fan, Tuomo Nieminen, Rami Lehtinen, Jari Viik, Kjell Nikus, Kari Niemelä, Tiit Kööbi, Väinö Turjanmaa, Ilkka Pörsti, Terho Lehtimäki.   

Abstract

T-wave alternans (TWA) in electrocardiography (ECG) is a marker of cardiac repolarization, the molecular regulation of which is incompletely understood. High TWA and prolonged QT intervals are both associated with ventricular arrhythmias and sudden death. Therefore, we tested the hypothesis of whether the same mutations that influence the QT interval also affect TWA variation. We examined the effect of 3 ion channel gene single nucleotide polymorphisms (SNPs), rs1805127, rs727957 KCNE1, and rs1805124 SCN5A, on TWA during a clinical exercise test. A total of 2008 subjects from the Finnish Cardiovascular Study underwent an exercise test with online ECG recording. TWA was measured by using the time-domain, modified moving average method. Maximum values at rest, during maximal exercise, and during recovery were used as outcome measures in statistical analysis. Moreover, 4-year survival data were collected and ion channel SNPs were determined. TWA was lowest in subjects with the TT genotype of rs1805127 during all phases of the exercise test (RANOVA main effect for genotype, P = 0.018). The result remained significant after adjustment for age, existing coronary heart disease, and beta-blocker medication status (RANCOVA, P = 0.035). Of the polymorphisms studied, only rs1805127 had a significant association with mortality (P = 0.047). The most common G-C haplotype, formed by rs727957 and rs1805127, was associated with TWA (RANOVA, P = 0.007) but not with mortality. The rs1805124 polymorphism was not associated with TWA. The common KCNE1 gene variant rs1805127 is associated with TWA during an exercise test in a Finnish population, which provides additional evidence that KCNE1 genetics may influence cardiac repolarization and cardiovascular mortality.

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Year:  2008        PMID: 18674739     DOI: 10.1016/j.trsl.2008.06.003

Source DB:  PubMed          Journal:  Transl Res        ISSN: 1878-1810            Impact factor:   7.012


  4 in total

1.  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

2.  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

3.  Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.

Authors:  Holger Herlyn; Ulrich Zechner; Franz Oswald; Arne Pfeufer; Hans Zischler; Thomas Haaf
Journal:  BMC Evol Biol       Date:  2009-08-06       Impact factor: 3.260

Review 4.  Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis.

Authors:  Xiaoli Liu; Jianli Shi; Peilin Xiao
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.817

  4 in total

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