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Characteristics of gut microbiota in patients with metabolic associated fatty liver disease

Metabolic associated fatty liver disease (MAFLD) is rising in incidence and is an increasingly common cause of cirrhosis and hepatocellular carcinoma (HCC). Alterations in the gut microbiota have been shown to correlate with the development and progression of MAFLD. However, little is known regardin...

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Autores principales: Yang, Chao, Xu, Jianguo, Xu, Xiaomin, Xu, Wen, Tong, Bangzhuo, Wang, Shulin, Ji, Rujie, Tan, Yan, Zhu, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281992/
https://www.ncbi.nlm.nih.gov/pubmed/37340081
http://dx.doi.org/10.1038/s41598-023-37163-4
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author Yang, Chao
Xu, Jianguo
Xu, Xiaomin
Xu, Wen
Tong, Bangzhuo
Wang, Shulin
Ji, Rujie
Tan, Yan
Zhu, Ying
author_facet Yang, Chao
Xu, Jianguo
Xu, Xiaomin
Xu, Wen
Tong, Bangzhuo
Wang, Shulin
Ji, Rujie
Tan, Yan
Zhu, Ying
author_sort Yang, Chao
collection PubMed
description Metabolic associated fatty liver disease (MAFLD) is rising in incidence and is an increasingly common cause of cirrhosis and hepatocellular carcinoma (HCC). Alterations in the gut microbiota have been shown to correlate with the development and progression of MAFLD. However, little is known regarding differences in the gut microbiomes of MAFLD patients and healthy cohorts, and subgroups at the abnormal activity of hepatic enzymes in China. In this study, we enrolled 81 MAFLD patients and 25 healthy volunteers. The fecal microbiota was assessed using 16S rRNA gene sequencing and metagenomic sequencing. The results suggested that Ruminococcus obeum and Alistipes were most enriched in healthy individuals when compared with MAFLD patients. Microbe‐set Enrichment Analysis (MSEA) results showed Dorea, Lactobacillus and Megasphaera are enriched in MAFLD group. We also found that Alistipes has negatively related to serum glucose (GLU), gamma-glutamyl transferase (GGT), and alanine aminotransferase (ALT). Moreover, the abundance of Dorea was found to be significantly overrepresented in the MAFLD patients and the degree of enrichment increased with the increasing abnormal liver enzyme. An increase in Dorea, combined with decreases in Alistipes appears to be characteristic of MAFLD patients. Further study of microbiota may provide a novel insight into the pathogenesis of MAFLD as well as a novel treatment strategy.
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spelling pubmed-102819922023-06-22 Characteristics of gut microbiota in patients with metabolic associated fatty liver disease Yang, Chao Xu, Jianguo Xu, Xiaomin Xu, Wen Tong, Bangzhuo Wang, Shulin Ji, Rujie Tan, Yan Zhu, Ying Sci Rep Article Metabolic associated fatty liver disease (MAFLD) is rising in incidence and is an increasingly common cause of cirrhosis and hepatocellular carcinoma (HCC). Alterations in the gut microbiota have been shown to correlate with the development and progression of MAFLD. However, little is known regarding differences in the gut microbiomes of MAFLD patients and healthy cohorts, and subgroups at the abnormal activity of hepatic enzymes in China. In this study, we enrolled 81 MAFLD patients and 25 healthy volunteers. The fecal microbiota was assessed using 16S rRNA gene sequencing and metagenomic sequencing. The results suggested that Ruminococcus obeum and Alistipes were most enriched in healthy individuals when compared with MAFLD patients. Microbe‐set Enrichment Analysis (MSEA) results showed Dorea, Lactobacillus and Megasphaera are enriched in MAFLD group. We also found that Alistipes has negatively related to serum glucose (GLU), gamma-glutamyl transferase (GGT), and alanine aminotransferase (ALT). Moreover, the abundance of Dorea was found to be significantly overrepresented in the MAFLD patients and the degree of enrichment increased with the increasing abnormal liver enzyme. An increase in Dorea, combined with decreases in Alistipes appears to be characteristic of MAFLD patients. Further study of microbiota may provide a novel insight into the pathogenesis of MAFLD as well as a novel treatment strategy. Nature Publishing Group UK 2023-06-20 /pmc/articles/PMC10281992/ /pubmed/37340081 http://dx.doi.org/10.1038/s41598-023-37163-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yang, Chao
Xu, Jianguo
Xu, Xiaomin
Xu, Wen
Tong, Bangzhuo
Wang, Shulin
Ji, Rujie
Tan, Yan
Zhu, Ying
Characteristics of gut microbiota in patients with metabolic associated fatty liver disease
title Characteristics of gut microbiota in patients with metabolic associated fatty liver disease
title_full Characteristics of gut microbiota in patients with metabolic associated fatty liver disease
title_fullStr Characteristics of gut microbiota in patients with metabolic associated fatty liver disease
title_full_unstemmed Characteristics of gut microbiota in patients with metabolic associated fatty liver disease
title_short Characteristics of gut microbiota in patients with metabolic associated fatty liver disease
title_sort characteristics of gut microbiota in patients with metabolic associated fatty liver disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281992/
https://www.ncbi.nlm.nih.gov/pubmed/37340081
http://dx.doi.org/10.1038/s41598-023-37163-4
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