Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram

Título traducido de la contribución: Veintiocho loci genéticos asociados con las amplitudes de onda ST-T del electrocardiograma

Niek Verweij, Irene Mateo Leach, Aaron Isaacs, Dan E. Arking, Joshua C. Bis, Tune H. Pers, Marten E. Van Den Berg, Leo Pekka Lyytikäinen, Phil Barnett, Xinchen Wang, Elsayed Z. Soliman, Cornelia M. Van Duijn, Mika Kähönen, Dirk J. Van Veldhuisen, Jan A. Kors, Olli T. Raitakari, Claudia T. Silva, Terho Lehtimäki, Hans L. Hillege, Joel N. HirschhornLaurie A. Boyer, Wiek H. Van Gilst, Alvaro Alonso, Nona Sotoodehnia, Mark Eijgelsheim, Rudolf A. De Boer, Paul I W De Bakker, Lude Franke, Pim Van Der Harst, Melanie van der Klauw, Gerjan Navis, Hans Ormel, Dirkje Postma, Judith Rosmalen, Joris Slaets, Ronald Stolk, Bruce Wolffenbuttel, Behrooz Alizadeh, Marike Boezen, Marcel Bruinenberg, Noortje Festen, Harold Snieder, Cisca Wijmenga

Resultado de la investigación: Contribución a RevistaArtículo

15 Citas (Scopus)

Resumen

El Autor 2016. El segmento ST y las amplitudes adyacentes de onda T (onda ST-T) del electrocardiograma son características cuantitativas de la repolarización cardiaca. Las anomalías de repolarización se han relacionado con arritmias ventriculares y muerte cardiaca súbita. Realizamos el primer metaanálisis de asociación de amplitudes de onda ST-T de todo el genoma en hasta 37 977 individuos, identificando 71 asociaciones robustas de genotipo-fenotipo agrupadas en 28 loci independientes. Cincuenta y cuatro genes fueron priorizados como candidatos subyacentes a los fenotipos, incluyendo genes con roles establecidos en la fase de repolarización cardiaca (SCN5A/SCN10A, KCND3, KCNB1, NOS1AP y HEY2) y otros con función cardiaca aún no definida. Estas asociaciones pueden proporcionar información sobre la contribución espacio temporal de la variación genética que influye en la repolarización cardiaca y proporcionar pistas novedosas para el seguimiento funcional futuro.
Idioma originalEnglish (US)
Páginas (desde-hasta)2093-2103
Número de páginas11
PublicaciónHuman Molecular Genetics
Volumen25
N.º10
DOI
EstadoPublished - may 15 2016

Huella dactilar

Genetic Loci
Electrocardiography
Genome-Wide Association Study
Sudden Cardiac Death
Genetic Association Studies
Genes
Meta-Analysis
Cardiac Arrhythmias
Phenotype

Citar esto

Verweij, N., Leach, I. M., Isaacs, A., Arking, D. E., Bis, J. C., Pers, T. H., ... Wijmenga, C. (2016). Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram. Human Molecular Genetics, 25(10), 2093-2103. https://doi.org/10.1093/hmg/ddw058
Verweij, Niek ; Leach, Irene Mateo ; Isaacs, Aaron ; Arking, Dan E. ; Bis, Joshua C. ; Pers, Tune H. ; Van Den Berg, Marten E. ; Lyytikäinen, Leo Pekka ; Barnett, Phil ; Wang, Xinchen ; 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. ; Boyer, Laurie A. ; 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 ; Klauw, Melanie van der ; Navis, Gerjan ; Ormel, Hans ; Postma, Dirkje ; Rosmalen, Judith ; Slaets, Joris ; Stolk, Ronald ; Wolffenbuttel, Bruce ; Alizadeh, Behrooz ; Boezen, Marike ; Bruinenberg, Marcel ; Festen, Noortje ; Snieder, Harold ; Wijmenga, Cisca. / Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram. En: Human Molecular Genetics. 2016 ; Vol. 25, N.º 10. pp. 2093-2103.
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title = "Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram",
abstract = "{\circledC} The Author 2016. Published by Oxford University Press.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.",
author = "Niek Verweij and Leach, {Irene Mateo} and Aaron Isaacs and Arking, {Dan E.} and Bis, {Joshua C.} and Pers, {Tune H.} and {Van Den Berg}, {Marten E.} and Lyytik{\"a}inen, {Leo Pekka} and Phil Barnett and Xinchen Wang and Soliman, {Elsayed Z.} and {Van Duijn}, {Cornelia M.} and Mika K{\"a}h{\"o}nen and {Van Veldhuisen}, {Dirk J.} and Kors, {Jan A.} and Raitakari, {Olli T.} and Silva, {Claudia T.} and Terho Lehtim{\"a}ki and Hillege, {Hans L.} and Hirschhorn, {Joel N.} and Boyer, {Laurie A.} and {Van Gilst}, {Wiek H.} and Alvaro Alonso and Nona Sotoodehnia and Mark Eijgelsheim and {De Boer}, {Rudolf A.} and {De Bakker}, {Paul I W} and Lude Franke and {Van Der Harst}, Pim and Klauw, {Melanie van der} and Gerjan Navis and Hans Ormel and Dirkje Postma and Judith Rosmalen and Joris Slaets and Ronald Stolk and Bruce Wolffenbuttel and Behrooz Alizadeh and Marike Boezen and Marcel Bruinenberg and Noortje Festen and Harold Snieder and Cisca Wijmenga",
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Verweij, N, Leach, IM, Isaacs, A, Arking, DE, Bis, JC, Pers, TH, Van Den Berg, ME, Lyytikäinen, LP, Barnett, P, Wang, X, Soliman, EZ, Van Duijn, CM, Kähönen, M, Van Veldhuisen, DJ, Kors, JA, Raitakari, OT, Silva, CT, Lehtimäki, T, Hillege, HL, Hirschhorn, JN, Boyer, LA, Van Gilst, WH, Alonso, A, Sotoodehnia, N, Eijgelsheim, M, De Boer, RA, De Bakker, PIW, Franke, L, Van Der Harst, P, Klauw, MVD, Navis, G, Ormel, H, Postma, D, Rosmalen, J, Slaets, J, Stolk, R, Wolffenbuttel, B, Alizadeh, B, Boezen, M, Bruinenberg, M, Festen, N, Snieder, H & Wijmenga, C 2016, 'Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram', Human Molecular Genetics, vol. 25, n.º 10, pp. 2093-2103. https://doi.org/10.1093/hmg/ddw058

Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram. / Verweij, Niek; Leach, Irene Mateo; Isaacs, Aaron; Arking, Dan E.; Bis, Joshua C.; Pers, Tune H.; Van Den Berg, Marten E.; Lyytikäinen, Leo Pekka; Barnett, Phil; Wang, Xinchen; 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.; Boyer, Laurie A.; 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; Klauw, Melanie van der; Navis, Gerjan; Ormel, Hans; Postma, Dirkje; Rosmalen, Judith; Slaets, Joris; Stolk, Ronald; Wolffenbuttel, Bruce; Alizadeh, Behrooz; Boezen, Marike; Bruinenberg, Marcel; Festen, Noortje; Snieder, Harold; Wijmenga, Cisca.

En: Human Molecular Genetics, Vol. 25, N.º 10, 15.05.2016, p. 2093-2103.

Resultado de la investigación: Contribución a RevistaArtículo

TY - JOUR

T1 - Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram

AU - Verweij, Niek

AU - Leach, Irene Mateo

AU - Isaacs, Aaron

AU - Arking, Dan E.

AU - Bis, Joshua C.

AU - Pers, Tune H.

AU - Van Den Berg, Marten E.

AU - Lyytikäinen, Leo Pekka

AU - Barnett, Phil

AU - Wang, Xinchen

AU - Soliman, Elsayed Z.

AU - Van Duijn, Cornelia M.

AU - Kähönen, Mika

AU - Van Veldhuisen, Dirk J.

AU - Kors, Jan A.

AU - Raitakari, Olli T.

AU - Silva, Claudia T.

AU - Lehtimäki, Terho

AU - Hillege, Hans L.

AU - Hirschhorn, Joel N.

AU - Boyer, Laurie A.

AU - Van Gilst, Wiek H.

AU - Alonso, Alvaro

AU - Sotoodehnia, Nona

AU - Eijgelsheim, Mark

AU - De Boer, Rudolf A.

AU - De Bakker, Paul I W

AU - Franke, Lude

AU - Van Der Harst, Pim

AU - Klauw, Melanie van der

AU - Navis, Gerjan

AU - Ormel, Hans

AU - Postma, Dirkje

AU - Rosmalen, Judith

AU - Slaets, Joris

AU - Stolk, Ronald

AU - Wolffenbuttel, Bruce

AU - Alizadeh, Behrooz

AU - Boezen, Marike

AU - Bruinenberg, Marcel

AU - Festen, Noortje

AU - Snieder, Harold

AU - Wijmenga, Cisca

PY - 2016/5/15

Y1 - 2016/5/15

N2 - © The Author 2016. Published by Oxford University Press.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.

AB - © The Author 2016. Published by Oxford University Press.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.

U2 - 10.1093/hmg/ddw058

DO - 10.1093/hmg/ddw058

M3 - Article

C2 - 26962151

VL - 25

SP - 2093

EP - 2103

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 10

ER -

Verweij N, Leach IM, Isaacs A, Arking DE, Bis JC, Pers TH y otros. Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram. Human Molecular Genetics. 2016 may 15;25(10):2093-2103. https://doi.org/10.1093/hmg/ddw058