Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver disease

Abstract Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD), is associated with altered gut microbiota; however, there has been a focus on fecal samples, which are not representative of the entire digestive tract. Mucosal biop...

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Main Authors: Mengting Ren, Hanghai Pan, Xinxin Zhou, Mosang Yu, Feng Ji
Format: Article
Language:English
Published: Nature Portfolio 2024-04-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-024-59605-3
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author Mengting Ren
Hanghai Pan
Xinxin Zhou
Mosang Yu
Feng Ji
author_facet Mengting Ren
Hanghai Pan
Xinxin Zhou
Mosang Yu
Feng Ji
author_sort Mengting Ren
collection DOAJ
description Abstract Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD), is associated with altered gut microbiota; however, there has been a focus on fecal samples, which are not representative of the entire digestive tract. Mucosal biopsies of the descending duodenum were collected. Five regions of the 16S rRNA gene were amplified and sequenced. Other assessments conducted on the study subjects included body mass index, transient elastography, liver enzymes, and lipid profile. Fifty-one subjects (36 with MASLD and 15 controls) were evaluated. There was no significant difference between the two groups regarding alpha- or beta-diversity of the duodenal mucosal microbiota. Linear discriminant analysis effect size (LEfSe) analysis showed that the genera Serratia and Aggregatibacter were more abundant in the duodenal mucosa of patients with MASLD, whereas the duodenal mucosal microbiota of the healthy controls was enriched with the genus Petrobacter. PICRUSt2 analysis revealed that genes associated with amino acid degradation and carboxylate degradation were significantly enriched in the duodenal mucosal microbiota of patients with MASLD. Our findings reveal the duodenal mucosal microbiota in patients with MASLD, which could contribute to future studies investigating the causal relationship between duodenal microbiota and MASLD.
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spelling doaj.art-fd1b96baf37e40b98aabf7c2e0d11c3d2024-04-21T11:14:19ZengNature PortfolioScientific Reports2045-23222024-04-011411910.1038/s41598-024-59605-3Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver diseaseMengting Ren0Hanghai Pan1Xinxin Zhou2Mosang Yu3Feng Ji4Department of Gastroenterology, The First Affiliated Hospital, Zhejiang University School of MedicineDepartment of Gastroenterology, The First Affiliated Hospital, Zhejiang University School of MedicineDepartment of Gastroenterology, The First Affiliated Hospital, Zhejiang University School of MedicineDepartment of Gastroenterology, The First Affiliated Hospital, Zhejiang University School of MedicineDepartment of Gastroenterology, The First Affiliated Hospital, Zhejiang University School of MedicineAbstract Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD), is associated with altered gut microbiota; however, there has been a focus on fecal samples, which are not representative of the entire digestive tract. Mucosal biopsies of the descending duodenum were collected. Five regions of the 16S rRNA gene were amplified and sequenced. Other assessments conducted on the study subjects included body mass index, transient elastography, liver enzymes, and lipid profile. Fifty-one subjects (36 with MASLD and 15 controls) were evaluated. There was no significant difference between the two groups regarding alpha- or beta-diversity of the duodenal mucosal microbiota. Linear discriminant analysis effect size (LEfSe) analysis showed that the genera Serratia and Aggregatibacter were more abundant in the duodenal mucosa of patients with MASLD, whereas the duodenal mucosal microbiota of the healthy controls was enriched with the genus Petrobacter. PICRUSt2 analysis revealed that genes associated with amino acid degradation and carboxylate degradation were significantly enriched in the duodenal mucosal microbiota of patients with MASLD. Our findings reveal the duodenal mucosal microbiota in patients with MASLD, which could contribute to future studies investigating the causal relationship between duodenal microbiota and MASLD.https://doi.org/10.1038/s41598-024-59605-3Gut microbiotaMetabolic dysfunction-associated steatotic liver diseaseSmall intestineMucosa-associated microbiota
spellingShingle Mengting Ren
Hanghai Pan
Xinxin Zhou
Mosang Yu
Feng Ji
Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver disease
Scientific Reports
Gut microbiota
Metabolic dysfunction-associated steatotic liver disease
Small intestine
Mucosa-associated microbiota
title Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver disease
title_full Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver disease
title_fullStr Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver disease
title_full_unstemmed Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver disease
title_short Alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction-associated steatotic liver disease
title_sort alterations of the duodenal mucosal microbiome in patients with metabolic dysfunction associated steatotic liver disease
topic Gut microbiota
Metabolic dysfunction-associated steatotic liver disease
Small intestine
Mucosa-associated microbiota
url https://doi.org/10.1038/s41598-024-59605-3
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