Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram
Author(s)
Verweij, Niek; Mateo Leach, Irene; Isaacs, Aaron; Arking, Dan E.; Bis, Joshua C.; Pers, Tune H.; Van Den Berg, Marten E.; Lyytikäinen, Leo-Pekka; Barnett, Phil; Soliman, Elsayed Z.; Van Duijn, Cornelia M.; Kähönen, Mika; Van Veldhuisen, Dirk J.; Kors, Jan A.; Raitakari, Olli T.; Silva, Claudia T.; Lehtimäki, Terho; Hillege, Hans L.; Hirschhorn, Joel N.; Van Gilst, Wiek H.; Alonso, Alvaro; Sotoodehnia, Nona; Eijgelsheim, Mark; De Boer, Rudolf A.; De Bakker, Paul I. W.; Franke, Lude; Van Der Harst, Pim; Wang, Xinchen; Boyer, Laurie Ann; ... Show more Show less
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The ST-segment and adjacent T-wave (ST-T wave) amplitudes of the electrocardiogram are quantitative characteristics of cardiac repolarization. Repolarization abnormalities have been linked to ventricular arrhythmias and sudden cardiac death. We performed the first genome-wide association meta-analysis of ST-T-wave amplitudes in up to 37 977 individuals identifying 71 robust genotype–phenotype associations clustered within 28 independent loci. Fifty-four genes were prioritized as candidates underlying the phenotypes, including genes with established roles in the cardiac repolarization phase (SCN5A/SCN10A, KCND3, KCNB1, NOS1AP and HEY2) and others with as yet undefined cardiac function. These associations may provide insights in the spatiotemporal contribution of genetic variation influencing cardiac repolarization and provide novel leads for future functional follow-up.
Date issued
2016-02Department
Massachusetts Institute of Technology. Department of BiologyJournal
Human Molecular Genetics
Publisher
Oxford University Press
Citation
Verweij, Niek et al. “Twenty-Eight Genetic Loci Associated with ST-T-Wave Amplitudes of the Electrocardiogram.” Human Molecular Genetics 25.10 (2016): 2093–2103.
Version: Final published version
ISSN
0964-6906
1460-2083