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Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system
Impaired capacity to increase heart rate (HR) during exercise (ΔHR(ex)), and a reduced rate of recovery post-exercise (ΔHR(rec)) are associated with higher cardiovascular mortality rates. Currently, the genetic basis of both phenotypes remains to be elucidated. We conduct genome-wide association stu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955978/ https://www.ncbi.nlm.nih.gov/pubmed/29769521 http://dx.doi.org/10.1038/s41467-018-04148-1 |
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author | Ramírez, Julia Duijvenboden, Stefan van Ntalla, Ioanna Mifsud, Borbala Warren, Helen R Tzanis, Evan Orini, Michele Tinker, Andrew Lambiase, Pier D. Munroe, Patricia B. |
author_facet | Ramírez, Julia Duijvenboden, Stefan van Ntalla, Ioanna Mifsud, Borbala Warren, Helen R Tzanis, Evan Orini, Michele Tinker, Andrew Lambiase, Pier D. Munroe, Patricia B. |
author_sort | Ramírez, Julia |
collection | PubMed |
description | Impaired capacity to increase heart rate (HR) during exercise (ΔHR(ex)), and a reduced rate of recovery post-exercise (ΔHR(rec)) are associated with higher cardiovascular mortality rates. Currently, the genetic basis of both phenotypes remains to be elucidated. We conduct genome-wide association studies (GWASs) for ΔHR(ex) and ΔHR(rec) in ~40,000 individuals, followed by replication in ~27,000 independent samples, all from UK Biobank. Six and seven single-nucleotide polymorphisms for ΔHR(ex) and ΔHR(rec), respectively, formally replicate. In a full data set GWAS, eight further loci for ΔHR(ex) and nine for ΔHR(rec) are genome-wide significant (P ≤ 5 × 10(−8)). In total, 30 loci are discovered, 8 being common across traits. Processes of neural development and modulation of adrenergic activity by the autonomic nervous system are enriched in these results. Our findings reinforce current understanding of HR response to exercise and recovery and could guide future studies evaluating its contribution to cardiovascular risk prediction. |
format | Online Article Text |
id | pubmed-5955978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59559782018-05-21 Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system Ramírez, Julia Duijvenboden, Stefan van Ntalla, Ioanna Mifsud, Borbala Warren, Helen R Tzanis, Evan Orini, Michele Tinker, Andrew Lambiase, Pier D. Munroe, Patricia B. Nat Commun Article Impaired capacity to increase heart rate (HR) during exercise (ΔHR(ex)), and a reduced rate of recovery post-exercise (ΔHR(rec)) are associated with higher cardiovascular mortality rates. Currently, the genetic basis of both phenotypes remains to be elucidated. We conduct genome-wide association studies (GWASs) for ΔHR(ex) and ΔHR(rec) in ~40,000 individuals, followed by replication in ~27,000 independent samples, all from UK Biobank. Six and seven single-nucleotide polymorphisms for ΔHR(ex) and ΔHR(rec), respectively, formally replicate. In a full data set GWAS, eight further loci for ΔHR(ex) and nine for ΔHR(rec) are genome-wide significant (P ≤ 5 × 10(−8)). In total, 30 loci are discovered, 8 being common across traits. Processes of neural development and modulation of adrenergic activity by the autonomic nervous system are enriched in these results. Our findings reinforce current understanding of HR response to exercise and recovery and could guide future studies evaluating its contribution to cardiovascular risk prediction. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955978/ /pubmed/29769521 http://dx.doi.org/10.1038/s41467-018-04148-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ramírez, Julia Duijvenboden, Stefan van Ntalla, Ioanna Mifsud, Borbala Warren, Helen R Tzanis, Evan Orini, Michele Tinker, Andrew Lambiase, Pier D. Munroe, Patricia B. Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system |
title | Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system |
title_full | Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system |
title_fullStr | Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system |
title_full_unstemmed | Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system |
title_short | Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system |
title_sort | thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955978/ https://www.ncbi.nlm.nih.gov/pubmed/29769521 http://dx.doi.org/10.1038/s41467-018-04148-1 |
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