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Cardiac autonomic control in the obstructive sleep apnea

INTRODUCTION: The sympathetic activation is considered to be the main mechanism involved in the development of cardiovascular diseases in obstructive sleep apnea (OSA). The heart rate variability (HRV) analysis represents a non-invasive tool allowing the study of the autonomic nervous system. The im...

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Autores principales: Gammoudi, Nouha, Ben Cheikh, Ridha, Saafi, Mohamed Ali, Sakly, Ghazi, Dogui, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393423/
https://www.ncbi.nlm.nih.gov/pubmed/25861821
http://dx.doi.org/10.3402/ljm.v10.26989
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author Gammoudi, Nouha
Ben Cheikh, Ridha
Saafi, Mohamed Ali
Sakly, Ghazi
Dogui, Mohamed
author_facet Gammoudi, Nouha
Ben Cheikh, Ridha
Saafi, Mohamed Ali
Sakly, Ghazi
Dogui, Mohamed
author_sort Gammoudi, Nouha
collection PubMed
description INTRODUCTION: The sympathetic activation is considered to be the main mechanism involved in the development of cardiovascular diseases in obstructive sleep apnea (OSA). The heart rate variability (HRV) analysis represents a non-invasive tool allowing the study of the autonomic nervous system. The impairment of HRV parameters in OSA has been documented. However, only a few studies tackled the dynamics of the autonomic nervous system during sleep in patients having OSA. AIMS: To analyze the HRV over sleep stages and across sleep periods in order to clarify the impact of OSA on cardiac autonomic modulation. The second objective is to examine the nocturnal HRV of OSA patients to find out which HRV parameter is the best to reflect the symptoms severity. METHODS: The study was retrospective. We have included 30 patients undergoing overnight polysomnography. Subjects were categorized into two groups according to apnea–hypopnea index (AHI): mild-to-moderate OSAS group (AHI: 5–30) and severe OSAS group (AHI>30). The HRV measures for participants with low apnea–hypopnea indices were compared to those of patients with high rates of apnea–hypopnea across the sleep period and sleep stages. RESULTS: HRV measures during sleep stages for the group with low rates of apnea–hypopnea have indicated a parasympathetic activation during non-rapid eye movement (NREM) sleep. However, no significant difference has been observed in the high AHI group except for the mean of RR intervals (mean RR). The parasympathetic activity tended to increase across the night but without a statistical difference. After control of age and body mass index, the most significant correlation found was for the mean RR (p=0.0001, r=−0.248). CONCLUSION: OSA affects sympathovagal modulation during sleep, and this impact has been correlated to the severity of the disease. The mean RR seemed to be a better index allowing the sympathovagal balance appreciation during the night in OSA.
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spelling pubmed-43934232015-04-16 Cardiac autonomic control in the obstructive sleep apnea Gammoudi, Nouha Ben Cheikh, Ridha Saafi, Mohamed Ali Sakly, Ghazi Dogui, Mohamed Libyan J Med Original Article INTRODUCTION: The sympathetic activation is considered to be the main mechanism involved in the development of cardiovascular diseases in obstructive sleep apnea (OSA). The heart rate variability (HRV) analysis represents a non-invasive tool allowing the study of the autonomic nervous system. The impairment of HRV parameters in OSA has been documented. However, only a few studies tackled the dynamics of the autonomic nervous system during sleep in patients having OSA. AIMS: To analyze the HRV over sleep stages and across sleep periods in order to clarify the impact of OSA on cardiac autonomic modulation. The second objective is to examine the nocturnal HRV of OSA patients to find out which HRV parameter is the best to reflect the symptoms severity. METHODS: The study was retrospective. We have included 30 patients undergoing overnight polysomnography. Subjects were categorized into two groups according to apnea–hypopnea index (AHI): mild-to-moderate OSAS group (AHI: 5–30) and severe OSAS group (AHI>30). The HRV measures for participants with low apnea–hypopnea indices were compared to those of patients with high rates of apnea–hypopnea across the sleep period and sleep stages. RESULTS: HRV measures during sleep stages for the group with low rates of apnea–hypopnea have indicated a parasympathetic activation during non-rapid eye movement (NREM) sleep. However, no significant difference has been observed in the high AHI group except for the mean of RR intervals (mean RR). The parasympathetic activity tended to increase across the night but without a statistical difference. After control of age and body mass index, the most significant correlation found was for the mean RR (p=0.0001, r=−0.248). CONCLUSION: OSA affects sympathovagal modulation during sleep, and this impact has been correlated to the severity of the disease. The mean RR seemed to be a better index allowing the sympathovagal balance appreciation during the night in OSA. Co-Action Publishing 2015-04-08 /pmc/articles/PMC4393423/ /pubmed/25861821 http://dx.doi.org/10.3402/ljm.v10.26989 Text en © 2015 Nouha Gammoudi et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gammoudi, Nouha
Ben Cheikh, Ridha
Saafi, Mohamed Ali
Sakly, Ghazi
Dogui, Mohamed
Cardiac autonomic control in the obstructive sleep apnea
title Cardiac autonomic control in the obstructive sleep apnea
title_full Cardiac autonomic control in the obstructive sleep apnea
title_fullStr Cardiac autonomic control in the obstructive sleep apnea
title_full_unstemmed Cardiac autonomic control in the obstructive sleep apnea
title_short Cardiac autonomic control in the obstructive sleep apnea
title_sort cardiac autonomic control in the obstructive sleep apnea
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393423/
https://www.ncbi.nlm.nih.gov/pubmed/25861821
http://dx.doi.org/10.3402/ljm.v10.26989
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