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)
Summary: | 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. |
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