Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram
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-analys...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2016
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/27140
- Acceso en línea:
- https://doi.org/10.1093/hmg/ddw058
https://repository.urosario.edu.co/handle/10336/27140
- Palabra clave:
- Phenotype
electrocardiogram
ST segment
Sudden cardiac death
T wave feature
Follow-up
Genes
Genome
Single
Nucleotide polymorphism
Genetics
Heart ventricular arrhythmia
Cardiac function
Scn5a
Gene
Genotype-phenotype
Association
Snos1ap gene
Scn10a gene
Imputation
- Rights
- License
- Abierto (Texto Completo)
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dd7f780f-5aab-489d-a185-52fe7796fcf2-1124687e2-b3d7-4d61-822c-7ebfb7213811-1a973d5a7-cb60-4a89-8167-f2811c5918b3-189f7a083-04b3-41ec-aa82-a2ab9902eea8-151851907-12020-08-19T14:41:07Z2020-08-19T14:41:07Z2016-03-08The 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.application/pdfhttps://doi.org/10.1093/hmg/ddw058ISSN: 0964-6906EISSN: 1460-2083https://repository.urosario.edu.co/handle/10336/27140engOxford University Press2103No. 102093Human Molecular GeneticsVol. 25Human Molecular Genetics, ISSN: 0964-6906;EISSN: 1460-2083, Vol.25, No.10 (15 May 2016); pp. 2093–2103https://academic.oup.com/hmg/article/25/10/2093/2236414Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Human Molecular Geneticsinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURPhenotypeelectrocardiogramST segmentSudden cardiac deathT wave featureFollow-upGenesGenomeSingleNucleotide polymorphismGeneticsHeart ventricular arrhythmiaCardiac functionScn5aGeneGenotype-phenotypeAssociationSnos1ap geneScn10a geneImputationTwenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogramVeintiocho loci genéticos asociados con amplitudes de onda ST-T del electrocardiogramaarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Verweij, NiekMateo Leach, IreneIsaacs, AaronArkin, Dan E.Silva, Claudia T.10336/27140oai:repository.urosario.edu.co:10336/271402021-06-03 00:50:06.421https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram |
dc.title.TranslatedTitle.spa.fl_str_mv |
Veintiocho loci genéticos asociados con amplitudes de onda ST-T del electrocardiograma |
title |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram |
spellingShingle |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram Phenotype electrocardiogram ST segment Sudden cardiac death T wave feature Follow-up Genes Genome Single Nucleotide polymorphism Genetics Heart ventricular arrhythmia Cardiac function Scn5a Gene Genotype-phenotype Association Snos1ap gene Scn10a gene Imputation |
title_short |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram |
title_full |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram |
title_fullStr |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram |
title_full_unstemmed |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram |
title_sort |
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram |
dc.subject.keyword.spa.fl_str_mv |
Phenotype electrocardiogram ST segment Sudden cardiac death T wave feature Follow-up Genes Genome Single Nucleotide polymorphism Genetics Heart ventricular arrhythmia Cardiac function Scn5a Gene Genotype-phenotype Association Snos1ap gene Scn10a gene Imputation |
topic |
Phenotype electrocardiogram ST segment Sudden cardiac death T wave feature Follow-up Genes Genome Single Nucleotide polymorphism Genetics Heart ventricular arrhythmia Cardiac function Scn5a Gene Genotype-phenotype Association Snos1ap gene Scn10a gene Imputation |
description |
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. |
publishDate |
2016 |
dc.date.created.spa.fl_str_mv |
2016-03-08 |
dc.date.accessioned.none.fl_str_mv |
2020-08-19T14:41:07Z |
dc.date.available.none.fl_str_mv |
2020-08-19T14:41:07Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1093/hmg/ddw058 |
dc.identifier.issn.none.fl_str_mv |
ISSN: 0964-6906 EISSN: 1460-2083 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/27140 |
url |
https://doi.org/10.1093/hmg/ddw058 https://repository.urosario.edu.co/handle/10336/27140 |
identifier_str_mv |
ISSN: 0964-6906 EISSN: 1460-2083 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
2103 |
dc.relation.citationIssue.none.fl_str_mv |
No. 10 |
dc.relation.citationStartPage.none.fl_str_mv |
2093 |
dc.relation.citationTitle.none.fl_str_mv |
Human Molecular Genetics |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 25 |
dc.relation.ispartof.spa.fl_str_mv |
Human Molecular Genetics, ISSN: 0964-6906;EISSN: 1460-2083, Vol.25, No.10 (15 May 2016); pp. 2093–2103 |
dc.relation.uri.spa.fl_str_mv |
https://academic.oup.com/hmg/article/25/10/2093/2236414 |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Oxford University Press |
dc.source.spa.fl_str_mv |
Human Molecular Genetics |
institution |
Universidad del Rosario |
dc.source.instname.none.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.none.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1814167600375005184 |