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Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis

Autonomic dysfunction is recognized to contribute to cardiovascular consequences in obstructive sleep apnea/hypopnea syndrome (OSAHS) patients who present predominant cardiovascular sympathetic activity that persists during wakefulness. Here, we examined 1) the factors that influence sympathetic car...

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Autores principales: Chouchou, Florian, Pichot, Vincent, Barthélémy, Jean-Claude, Bastuji, Hélène, Roche, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899280/
https://www.ncbi.nlm.nih.gov/pubmed/24466093
http://dx.doi.org/10.1371/journal.pone.0086434
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author Chouchou, Florian
Pichot, Vincent
Barthélémy, Jean-Claude
Bastuji, Hélène
Roche, Frédéric
author_facet Chouchou, Florian
Pichot, Vincent
Barthélémy, Jean-Claude
Bastuji, Hélène
Roche, Frédéric
author_sort Chouchou, Florian
collection PubMed
description Autonomic dysfunction is recognized to contribute to cardiovascular consequences in obstructive sleep apnea/hypopnea syndrome (OSAHS) patients who present predominant cardiovascular sympathetic activity that persists during wakefulness. Here, we examined 1) the factors that influence sympathetic cardiac modulation in response to apneas/hypopneas; and 2) the influence of autonomic activity during apneas/hypopneas on CA. Sixteen OSAHS patients underwent in-hospital polysomnography. RR interval (RR) and RR spectral analysis using wavelet transform were used to study parasympathetic (high frequency power: HF(WV)) and sympathetic (low frequency power: LF(WV) and LF(WV)/HF(WV) ratio) activity before and after apnea/hypopnea termination. Autonomic cardiac modulations were compared according to sleep stage, apnea/hypopnea type and duration, arterial oxygen saturation, and presence of CA. At apnea/hypopnea termination, RR decreased (p<0.001) while LF(WV) (p = 0.001) and LF(WV)/HF(WV) ratio (p = 0.001) increased. Only RR and LF(WV)/HF(WV) ratio changes were higher when apneas/hypopneas produced CA (p = 0.030 and p = 0.035, respectively) or deep hypoxia (p = 0.023 and p = 0.046, respectively). Multivariate statistical analysis showed that elevated LF(WV) (p = 0.006) and LF(WV)/HF(WV) ratio (p = 0.029) during apneas/hypopneas were independently related to higher CA occurrence. Both the arousal and hypoxia processes may contribute to sympathetic cardiovascular overactivity by recurrent cardiac sympathetic modulation in response to apneas/hypopneas. Sympathetic overactivity also may play an important role in the acute central response to apneas/hypopneas, and in the sleep fragmentation.
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spelling pubmed-38992802014-01-24 Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis Chouchou, Florian Pichot, Vincent Barthélémy, Jean-Claude Bastuji, Hélène Roche, Frédéric PLoS One Research Article Autonomic dysfunction is recognized to contribute to cardiovascular consequences in obstructive sleep apnea/hypopnea syndrome (OSAHS) patients who present predominant cardiovascular sympathetic activity that persists during wakefulness. Here, we examined 1) the factors that influence sympathetic cardiac modulation in response to apneas/hypopneas; and 2) the influence of autonomic activity during apneas/hypopneas on CA. Sixteen OSAHS patients underwent in-hospital polysomnography. RR interval (RR) and RR spectral analysis using wavelet transform were used to study parasympathetic (high frequency power: HF(WV)) and sympathetic (low frequency power: LF(WV) and LF(WV)/HF(WV) ratio) activity before and after apnea/hypopnea termination. Autonomic cardiac modulations were compared according to sleep stage, apnea/hypopnea type and duration, arterial oxygen saturation, and presence of CA. At apnea/hypopnea termination, RR decreased (p<0.001) while LF(WV) (p = 0.001) and LF(WV)/HF(WV) ratio (p = 0.001) increased. Only RR and LF(WV)/HF(WV) ratio changes were higher when apneas/hypopneas produced CA (p = 0.030 and p = 0.035, respectively) or deep hypoxia (p = 0.023 and p = 0.046, respectively). Multivariate statistical analysis showed that elevated LF(WV) (p = 0.006) and LF(WV)/HF(WV) ratio (p = 0.029) during apneas/hypopneas were independently related to higher CA occurrence. Both the arousal and hypoxia processes may contribute to sympathetic cardiovascular overactivity by recurrent cardiac sympathetic modulation in response to apneas/hypopneas. Sympathetic overactivity also may play an important role in the acute central response to apneas/hypopneas, and in the sleep fragmentation. Public Library of Science 2014-01-22 /pmc/articles/PMC3899280/ /pubmed/24466093 http://dx.doi.org/10.1371/journal.pone.0086434 Text en © 2014 Chouchou et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chouchou, Florian
Pichot, Vincent
Barthélémy, Jean-Claude
Bastuji, Hélène
Roche, Frédéric
Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis
title Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis
title_full Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis
title_fullStr Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis
title_full_unstemmed Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis
title_short Cardiac Sympathetic Modulation in Response to Apneas/Hypopneas through Heart Rate Variability Analysis
title_sort cardiac sympathetic modulation in response to apneas/hypopneas through heart rate variability analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899280/
https://www.ncbi.nlm.nih.gov/pubmed/24466093
http://dx.doi.org/10.1371/journal.pone.0086434
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