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Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea
BACKGROUND: Several clinical studies have demonstrated that pediatric obstructive sleep apnea (OSA) is associated with dysbiosis of airway mucosal microbiota. However, how oral and nasal microbial diversity, composition, and structure are altered in pediatric OSA has not been systemically explored....
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980019/ https://www.ncbi.nlm.nih.gov/pubmed/36875426 http://dx.doi.org/10.1080/20002297.2023.2182571 |
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author | Zhang, Xiaoman Li, Xinyi Xu, Huajun Fu, Zhihui Wang, Fan Huang, Weijun Wu, Kejia Li, Chenyang Liu, Yupu Zou, Jianyin Zhu, Huaming Yi, Hongliang Kaiming, Su Gu, Meizhen Guan, Jian Yin, Shankai |
author_facet | Zhang, Xiaoman Li, Xinyi Xu, Huajun Fu, Zhihui Wang, Fan Huang, Weijun Wu, Kejia Li, Chenyang Liu, Yupu Zou, Jianyin Zhu, Huaming Yi, Hongliang Kaiming, Su Gu, Meizhen Guan, Jian Yin, Shankai |
author_sort | Zhang, Xiaoman |
collection | PubMed |
description | BACKGROUND: Several clinical studies have demonstrated that pediatric obstructive sleep apnea (OSA) is associated with dysbiosis of airway mucosal microbiota. However, how oral and nasal microbial diversity, composition, and structure are altered in pediatric OSA has not been systemically explored. METHODS: 30 polysomnography-confirmed OSA patients with adenoid hypertrophy, and 30 controls who did not have adenoid hypertrophy, were enrolled. Swabs from four surface oral tissue sites (tongue base, soft palate, both palatine tonsils, and adenoid) and one nasal swab from both anterior nares were collected. The 16S ribosomal RNA (rRNA) V3–V4 region was sequenced to identify the microbial communities. RESULTS: The beta diversity and microbial profiles were significantly different between pediatric OSA patients and controls at the five upper airway sites. The abundances of Haemophilus, Fusobacterium, and Porphyromonas were higher at adenoid and tonsils sites of pediatric patients with OSA. Functional analysis revealed that the differential pathway between the pediatric OSA patients and controls involved glycerophospholipids and amino acid metabolism. CONCLUSIONS: In this study, the oral and nasal microbiome of pediatric OSA patients exhibited certain differences in composition compared with the controls. However, the microbiota data could be useful as a reference for studies on the upper airway microbiome. |
format | Online Article Text |
id | pubmed-9980019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-99800192023-03-03 Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea Zhang, Xiaoman Li, Xinyi Xu, Huajun Fu, Zhihui Wang, Fan Huang, Weijun Wu, Kejia Li, Chenyang Liu, Yupu Zou, Jianyin Zhu, Huaming Yi, Hongliang Kaiming, Su Gu, Meizhen Guan, Jian Yin, Shankai J Oral Microbiol Original Article BACKGROUND: Several clinical studies have demonstrated that pediatric obstructive sleep apnea (OSA) is associated with dysbiosis of airway mucosal microbiota. However, how oral and nasal microbial diversity, composition, and structure are altered in pediatric OSA has not been systemically explored. METHODS: 30 polysomnography-confirmed OSA patients with adenoid hypertrophy, and 30 controls who did not have adenoid hypertrophy, were enrolled. Swabs from four surface oral tissue sites (tongue base, soft palate, both palatine tonsils, and adenoid) and one nasal swab from both anterior nares were collected. The 16S ribosomal RNA (rRNA) V3–V4 region was sequenced to identify the microbial communities. RESULTS: The beta diversity and microbial profiles were significantly different between pediatric OSA patients and controls at the five upper airway sites. The abundances of Haemophilus, Fusobacterium, and Porphyromonas were higher at adenoid and tonsils sites of pediatric patients with OSA. Functional analysis revealed that the differential pathway between the pediatric OSA patients and controls involved glycerophospholipids and amino acid metabolism. CONCLUSIONS: In this study, the oral and nasal microbiome of pediatric OSA patients exhibited certain differences in composition compared with the controls. However, the microbiota data could be useful as a reference for studies on the upper airway microbiome. Taylor & Francis 2023-02-28 /pmc/articles/PMC9980019/ /pubmed/36875426 http://dx.doi.org/10.1080/20002297.2023.2182571 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Zhang, Xiaoman Li, Xinyi Xu, Huajun Fu, Zhihui Wang, Fan Huang, Weijun Wu, Kejia Li, Chenyang Liu, Yupu Zou, Jianyin Zhu, Huaming Yi, Hongliang Kaiming, Su Gu, Meizhen Guan, Jian Yin, Shankai Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea |
title | Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea |
title_full | Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea |
title_fullStr | Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea |
title_full_unstemmed | Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea |
title_short | Changes in the oral and nasal microbiota in pediatric obstructive sleep apnea |
title_sort | changes in the oral and nasal microbiota in pediatric obstructive sleep apnea |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980019/ https://www.ncbi.nlm.nih.gov/pubmed/36875426 http://dx.doi.org/10.1080/20002297.2023.2182571 |
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