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The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model
The control mechanisms and implications of heart rate variability (HRV) under the sympathetic (SNS) and parasympathetic nervous system (PNS) modulation remain poorly understood. Here, we establish the HR model/HRV responder using a nonlinear process derived from Newton’s second law in stochastic sel...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075874/ https://www.ncbi.nlm.nih.gov/pubmed/32179768 http://dx.doi.org/10.1038/s41598-020-61562-6 |
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author | He, Zonglu |
author_facet | He, Zonglu |
author_sort | He, Zonglu |
collection | PubMed |
description | The control mechanisms and implications of heart rate variability (HRV) under the sympathetic (SNS) and parasympathetic nervous system (PNS) modulation remain poorly understood. Here, we establish the HR model/HRV responder using a nonlinear process derived from Newton’s second law in stochastic self-restoring systems through dynamic analysis of physiological properties. We conduct model validation by testing, predictions, simulations, and sensitivity and time-scale analysis. We confirm that the outputs of the HRV responder can be accepted as the real data-generating process. Empirical studies show that the dynamic control mechanism of heart rate is a stable fixed point, rather than a strange attractor or transitions between a fixed point and a limit cycle; HR slope (amplitude) may depend on the ratio of cardiac disturbance or metabolic demand mean (standard deviation) to myocardial electrical resistance (PNS-SNS activity). For example, when metabolic demands remain unchanged, HR amplitude depends on PNS to SNS activity; when autonomic activity remains unchanged, HR amplitude during resting reflects basal metabolism. HR parameter alterations suggest that age-related decreased HRV, ultrareduced HRV in heart failure, and ultraelevated HRV in ST segment alterations refer to age-related decreased basal metabolism, impaired myocardial metabolism, and SNS hyperactivity triggered by myocardial ischemia, respectively. |
format | Online Article Text |
id | pubmed-7075874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70758742020-03-22 The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model He, Zonglu Sci Rep Article The control mechanisms and implications of heart rate variability (HRV) under the sympathetic (SNS) and parasympathetic nervous system (PNS) modulation remain poorly understood. Here, we establish the HR model/HRV responder using a nonlinear process derived from Newton’s second law in stochastic self-restoring systems through dynamic analysis of physiological properties. We conduct model validation by testing, predictions, simulations, and sensitivity and time-scale analysis. We confirm that the outputs of the HRV responder can be accepted as the real data-generating process. Empirical studies show that the dynamic control mechanism of heart rate is a stable fixed point, rather than a strange attractor or transitions between a fixed point and a limit cycle; HR slope (amplitude) may depend on the ratio of cardiac disturbance or metabolic demand mean (standard deviation) to myocardial electrical resistance (PNS-SNS activity). For example, when metabolic demands remain unchanged, HR amplitude depends on PNS to SNS activity; when autonomic activity remains unchanged, HR amplitude during resting reflects basal metabolism. HR parameter alterations suggest that age-related decreased HRV, ultrareduced HRV in heart failure, and ultraelevated HRV in ST segment alterations refer to age-related decreased basal metabolism, impaired myocardial metabolism, and SNS hyperactivity triggered by myocardial ischemia, respectively. Nature Publishing Group UK 2020-03-16 /pmc/articles/PMC7075874/ /pubmed/32179768 http://dx.doi.org/10.1038/s41598-020-61562-6 Text en © The Author(s) 2020 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 He, Zonglu The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model |
title | The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model |
title_full | The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model |
title_fullStr | The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model |
title_full_unstemmed | The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model |
title_short | The control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model |
title_sort | control mechanisms of heart rate dynamics in a new heart rate nonlinear time series model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075874/ https://www.ncbi.nlm.nih.gov/pubmed/32179768 http://dx.doi.org/10.1038/s41598-020-61562-6 |
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