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Alterations of oral microbiota are associated with the development and severity of acute pancreatitis
Acute pancreatitis (AP) is a common abdomen clinical emergency. Most APs have mild clinical symptoms and a good prognosis. However, about 20% of patients develop severe acute pancreatitis (SAP), increasing morbidity and mortality. The microbiome’s impact on AP pathophysiology has received increasing...
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/PMC10557549/ https://www.ncbi.nlm.nih.gov/pubmed/37808891 http://dx.doi.org/10.1080/20002297.2023.2264619 |
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author | Liu, Yiting Liu, Hang Rong, Yuping Shi, Qiao Yang, Qiang Li, Hanjun Zhang, Zhengle Tao, Jing |
author_facet | Liu, Yiting Liu, Hang Rong, Yuping Shi, Qiao Yang, Qiang Li, Hanjun Zhang, Zhengle Tao, Jing |
author_sort | Liu, Yiting |
collection | PubMed |
description | Acute pancreatitis (AP) is a common abdomen clinical emergency. Most APs have mild clinical symptoms and a good prognosis. However, about 20% of patients develop severe acute pancreatitis (SAP), increasing morbidity and mortality. The microbiome’s impact on AP pathophysiology has received increasing attention. Hence, to explore changes in oral microbial composition in acute pancreatitis, we collected clinical information and oral saliva samples from 136 adult participants: 47 healthy controls, 43 acute mild AP (MAP), 29 moderate AP (MSAP), and 17 severe AP (SAP). Using 16S rRNA gene sequencing, 663,175 high-quality sequences were identified. The relative abundance and diversity of oral microorganisms in AP patients increased, with decreased beneficial bacteria such as Streptococcus, Neisseria, and Gemella, and increased Prevotella, Veillonella, Granulicatella, Actinomyces, and Peptostreptococcus in the AP group. Further changes in microbial composition occurred with increasing disease severity, including a decreased abundance of beneficial bacteria such as Neisseria, Haemophilus, and Gemella in MSAP and SAP compared to MAP. Moreover, the Lefse analysis showed that Prevotella, Peptostreptococcus, Actinomyces, and Porphyromonas were better microbial markers for AP. Therefore, oral microbiome changes could distinguish AP from healthy individuals and serve as an early novel predictor of disease severity in AP patients. |
format | Online Article Text |
id | pubmed-10557549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-105575492023-10-07 Alterations of oral microbiota are associated with the development and severity of acute pancreatitis Liu, Yiting Liu, Hang Rong, Yuping Shi, Qiao Yang, Qiang Li, Hanjun Zhang, Zhengle Tao, Jing J Oral Microbiol Research Article Acute pancreatitis (AP) is a common abdomen clinical emergency. Most APs have mild clinical symptoms and a good prognosis. However, about 20% of patients develop severe acute pancreatitis (SAP), increasing morbidity and mortality. The microbiome’s impact on AP pathophysiology has received increasing attention. Hence, to explore changes in oral microbial composition in acute pancreatitis, we collected clinical information and oral saliva samples from 136 adult participants: 47 healthy controls, 43 acute mild AP (MAP), 29 moderate AP (MSAP), and 17 severe AP (SAP). Using 16S rRNA gene sequencing, 663,175 high-quality sequences were identified. The relative abundance and diversity of oral microorganisms in AP patients increased, with decreased beneficial bacteria such as Streptococcus, Neisseria, and Gemella, and increased Prevotella, Veillonella, Granulicatella, Actinomyces, and Peptostreptococcus in the AP group. Further changes in microbial composition occurred with increasing disease severity, including a decreased abundance of beneficial bacteria such as Neisseria, Haemophilus, and Gemella in MSAP and SAP compared to MAP. Moreover, the Lefse analysis showed that Prevotella, Peptostreptococcus, Actinomyces, and Porphyromonas were better microbial markers for AP. Therefore, oral microbiome changes could distinguish AP from healthy individuals and serve as an early novel predictor of disease severity in AP patients. Taylor & Francis 2023-10-05 /pmc/articles/PMC10557549/ /pubmed/37808891 http://dx.doi.org/10.1080/20002297.2023.2264619 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. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Research Article Liu, Yiting Liu, Hang Rong, Yuping Shi, Qiao Yang, Qiang Li, Hanjun Zhang, Zhengle Tao, Jing Alterations of oral microbiota are associated with the development and severity of acute pancreatitis |
title | Alterations of oral microbiota are associated with the development and severity of acute pancreatitis |
title_full | Alterations of oral microbiota are associated with the development and severity of acute pancreatitis |
title_fullStr | Alterations of oral microbiota are associated with the development and severity of acute pancreatitis |
title_full_unstemmed | Alterations of oral microbiota are associated with the development and severity of acute pancreatitis |
title_short | Alterations of oral microbiota are associated with the development and severity of acute pancreatitis |
title_sort | alterations of oral microbiota are associated with the development and severity of acute pancreatitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557549/ https://www.ncbi.nlm.nih.gov/pubmed/37808891 http://dx.doi.org/10.1080/20002297.2023.2264619 |
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