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Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome

INTRODUCTION: Intermittent hypoxia and sleep fragmentation are critical pathophysiological processes involved in obstructive sleep apnea‐hypopnea syndrome (OSAHS). Those manifestations independently affect similar brain regions and contribute to OSAHS‐related comorbidities that are known to be relat...

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Autores principales: Ko, Chih‐Yuan, Fan, Ji‐Mim, Hu, An‐Ke, Su, Huan‐Zhang, Yang, Jiao‐Hong, Huang, Li‐Mei, Yan, Fu‐Rong, Zhang, Hua‐Ping, Zeng, Yi‐Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520469/
https://www.ncbi.nlm.nih.gov/pubmed/30957979
http://dx.doi.org/10.1002/brb3.1287
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author Ko, Chih‐Yuan
Fan, Ji‐Mim
Hu, An‐Ke
Su, Huan‐Zhang
Yang, Jiao‐Hong
Huang, Li‐Mei
Yan, Fu‐Rong
Zhang, Hua‐Ping
Zeng, Yi‐Ming
author_facet Ko, Chih‐Yuan
Fan, Ji‐Mim
Hu, An‐Ke
Su, Huan‐Zhang
Yang, Jiao‐Hong
Huang, Li‐Mei
Yan, Fu‐Rong
Zhang, Hua‐Ping
Zeng, Yi‐Ming
author_sort Ko, Chih‐Yuan
collection PubMed
description INTRODUCTION: Intermittent hypoxia and sleep fragmentation are critical pathophysiological processes involved in obstructive sleep apnea‐hypopnea syndrome (OSAHS). Those manifestations independently affect similar brain regions and contribute to OSAHS‐related comorbidities that are known to be related to the host gut alteration microbiota. We hypothesized that gut microbiota disruption may cross talk the brain function via the microbiota–gut–brain axis. Thus, we aim to survey enterotypes and polysomnographic data of patients with OSAHS. METHODS: Subjects were diagnosed by polysomnography, from whom fecal samples were obtained and analyzed for the microbiome composition by variable regions 3–4 of 16S rRNA pyrosequencing and bioinformatic analyses. We examined the fasting levels of interleukin‐6 and tumor necrosis factor‐alpha of all subjects. RESULTS: Three enterotypes Bacteroides, Ruminococcus, and Prevotella were identified in patients with OSAHS. Arousal‐related parameters or sleep stages are significantly disrupted in apnea‐hypopnea index (AHI) ≥15 patients with Prevotella enterotype; further analysis this enterotype subjects, obstructive, central, and mixed apnea indices, and mean heart rate are also significantly elevated in AHI ≥15 patients. However, blood cytokines levels of all subjects were not significantly different. CONCLUSIONS: This study indicates the possibility of pathophysiological interplay between enterotypes and sleeps structure disruption in sleep apnea through a microbiota–gut–brain axis and offers some new insight toward the pathogenesis of OSAHS.
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spelling pubmed-65204692019-05-23 Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome Ko, Chih‐Yuan Fan, Ji‐Mim Hu, An‐Ke Su, Huan‐Zhang Yang, Jiao‐Hong Huang, Li‐Mei Yan, Fu‐Rong Zhang, Hua‐Ping Zeng, Yi‐Ming Brain Behav Original Research INTRODUCTION: Intermittent hypoxia and sleep fragmentation are critical pathophysiological processes involved in obstructive sleep apnea‐hypopnea syndrome (OSAHS). Those manifestations independently affect similar brain regions and contribute to OSAHS‐related comorbidities that are known to be related to the host gut alteration microbiota. We hypothesized that gut microbiota disruption may cross talk the brain function via the microbiota–gut–brain axis. Thus, we aim to survey enterotypes and polysomnographic data of patients with OSAHS. METHODS: Subjects were diagnosed by polysomnography, from whom fecal samples were obtained and analyzed for the microbiome composition by variable regions 3–4 of 16S rRNA pyrosequencing and bioinformatic analyses. We examined the fasting levels of interleukin‐6 and tumor necrosis factor‐alpha of all subjects. RESULTS: Three enterotypes Bacteroides, Ruminococcus, and Prevotella were identified in patients with OSAHS. Arousal‐related parameters or sleep stages are significantly disrupted in apnea‐hypopnea index (AHI) ≥15 patients with Prevotella enterotype; further analysis this enterotype subjects, obstructive, central, and mixed apnea indices, and mean heart rate are also significantly elevated in AHI ≥15 patients. However, blood cytokines levels of all subjects were not significantly different. CONCLUSIONS: This study indicates the possibility of pathophysiological interplay between enterotypes and sleeps structure disruption in sleep apnea through a microbiota–gut–brain axis and offers some new insight toward the pathogenesis of OSAHS. John Wiley and Sons Inc. 2019-04-08 /pmc/articles/PMC6520469/ /pubmed/30957979 http://dx.doi.org/10.1002/brb3.1287 Text en © 2019 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Ko, Chih‐Yuan
Fan, Ji‐Mim
Hu, An‐Ke
Su, Huan‐Zhang
Yang, Jiao‐Hong
Huang, Li‐Mei
Yan, Fu‐Rong
Zhang, Hua‐Ping
Zeng, Yi‐Ming
Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome
title Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome
title_full Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome
title_fullStr Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome
title_full_unstemmed Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome
title_short Disruption of sleep architecture in Prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome
title_sort disruption of sleep architecture in prevotella enterotype of patients with obstructive sleep apnea‐hypopnea syndrome
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520469/
https://www.ncbi.nlm.nih.gov/pubmed/30957979
http://dx.doi.org/10.1002/brb3.1287
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