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Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study
BACKGROUND: Autonomic dysfunction appears to play a significant role in the development of atrial fibrillation (AF), and impaired heart rate recovery (HRR) during exercise treadmill testing (ETT) is a known marker for autonomic dysfunction. However, whether impaired HRR is associated with incident A...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660286/ https://www.ncbi.nlm.nih.gov/pubmed/19284627 http://dx.doi.org/10.1186/1471-2261-9-11 |
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author | Maddox, Thomas M Ross, Colleen Ho, P Michael Magid, David Rumsfeld, John S |
author_facet | Maddox, Thomas M Ross, Colleen Ho, P Michael Magid, David Rumsfeld, John S |
author_sort | Maddox, Thomas M |
collection | PubMed |
description | BACKGROUND: Autonomic dysfunction appears to play a significant role in the development of atrial fibrillation (AF), and impaired heart rate recovery (HRR) during exercise treadmill testing (ETT) is a known marker for autonomic dysfunction. However, whether impaired HRR is associated with incident AF is unknown. We studied the association of impaired HRR with the development of incident AF, after controlling for demographic and clinical confounders. METHODS: We studied 8236 patients referred for ETT between 2001 and 2004, and without a prior history of AF. Patients were categorized by normal or impaired HRR on ETT. The primary outcome was the development of AF. Cox proportional hazards modeling was used to control for demographic and clinical characteristics. Secondary analyses exploring a continuous relationship between impaired HRR and AF, and exploring interactions between cardiac medication use, HRR, and AF were also conducted. RESULTS: After adjustment, patients with impaired HRR were more likely to develop AF than patients with normal HRR (HR 1.43, 95% confidence interval (CI) 1.06, 1.93). In addition, there was a linear trend between impaired HRR and AF (HR 1.05 for each decreasing BPM in HRR, 95% CI 0.99, 1.11). No interactions between cardiac medications, HRR, and AF were noted. CONCLUSION: Patients with impaired HRR on ETT were more likely to develop new-onset AF, as compared to patients with normal HRR. These findings support the hypothesis that autonomic dysfunction mediates the development of AF, and suggest that interventions known to improve HRR, such as exercise training, may delay or prevent AF. |
format | Text |
id | pubmed-2660286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26602862009-03-25 Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study Maddox, Thomas M Ross, Colleen Ho, P Michael Magid, David Rumsfeld, John S BMC Cardiovasc Disord Research Article BACKGROUND: Autonomic dysfunction appears to play a significant role in the development of atrial fibrillation (AF), and impaired heart rate recovery (HRR) during exercise treadmill testing (ETT) is a known marker for autonomic dysfunction. However, whether impaired HRR is associated with incident AF is unknown. We studied the association of impaired HRR with the development of incident AF, after controlling for demographic and clinical confounders. METHODS: We studied 8236 patients referred for ETT between 2001 and 2004, and without a prior history of AF. Patients were categorized by normal or impaired HRR on ETT. The primary outcome was the development of AF. Cox proportional hazards modeling was used to control for demographic and clinical characteristics. Secondary analyses exploring a continuous relationship between impaired HRR and AF, and exploring interactions between cardiac medication use, HRR, and AF were also conducted. RESULTS: After adjustment, patients with impaired HRR were more likely to develop AF than patients with normal HRR (HR 1.43, 95% confidence interval (CI) 1.06, 1.93). In addition, there was a linear trend between impaired HRR and AF (HR 1.05 for each decreasing BPM in HRR, 95% CI 0.99, 1.11). No interactions between cardiac medications, HRR, and AF were noted. CONCLUSION: Patients with impaired HRR on ETT were more likely to develop new-onset AF, as compared to patients with normal HRR. These findings support the hypothesis that autonomic dysfunction mediates the development of AF, and suggest that interventions known to improve HRR, such as exercise training, may delay or prevent AF. BioMed Central 2009-03-12 /pmc/articles/PMC2660286/ /pubmed/19284627 http://dx.doi.org/10.1186/1471-2261-9-11 Text en Copyright © 2009 Maddox et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Maddox, Thomas M Ross, Colleen Ho, P Michael Magid, David Rumsfeld, John S Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study |
title | Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study |
title_full | Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study |
title_fullStr | Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study |
title_full_unstemmed | Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study |
title_short | Impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study |
title_sort | impaired heart rate recovery is associated with new-onset atrial fibrillation: a prospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660286/ https://www.ncbi.nlm.nih.gov/pubmed/19284627 http://dx.doi.org/10.1186/1471-2261-9-11 |
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