The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota

Several animal studies have emphasized the role of gut microbiota in nonalcoholic fatty liver disease (NAFLD). However, data about gut dysbiosis in human NAFLD remain scarce in the literature, especially studies including the whole spectrum of NAFLD lesions. We aimed to evaluate the association betw...

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Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2016-03, Vol.63 (3), p.764-775
Hauptverfasser: Boursier, Jérôme, Mueller, Olaf, Barret, Matthieu, Machado, Mariana, Fizanne, Lionel, Araujo‐Perez, Felix, Guy, Cynthia D., Seed, Patrick C., Rawls, John F., David, Lawrence A., Hunault, Gilles, Oberti, Frédéric, Calès, Paul, Diehl, Anna Mae
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container_issue 3
container_start_page 764
container_title Hepatology (Baltimore, Md.)
container_volume 63
creator Boursier, Jérôme
Mueller, Olaf
Barret, Matthieu
Machado, Mariana
Fizanne, Lionel
Araujo‐Perez, Felix
Guy, Cynthia D.
Seed, Patrick C.
Rawls, John F.
David, Lawrence A.
Hunault, Gilles
Oberti, Frédéric
Calès, Paul
Diehl, Anna Mae
description Several animal studies have emphasized the role of gut microbiota in nonalcoholic fatty liver disease (NAFLD). However, data about gut dysbiosis in human NAFLD remain scarce in the literature, especially studies including the whole spectrum of NAFLD lesions. We aimed to evaluate the association between gut dysbiosis and severe NAFLD lesions, that is, nonalcoholic steatohepatitis (NASH) and fibrosis, in a well‐characterized population of adult NAFLD. Fifty‐seven patients with biopsy‐proven NAFLD were enrolled. Taxonomic composition of gut microbiota was determined using 16S ribosomal RNA gene sequencing of stool samples. Thirty patients had F0/F1 fibrosis stage at liver biopsy (10 with NASH), and 27 patients had significant F≥2 fibrosis (25 with NASH). Bacteroides abundance was significantly increased in NASH and F≥2 patients, whereas Prevotella abundance was decreased. Ruminococcus abundance was significantly higher in F≥2 patients. By multivariate analysis, Bacteroides abundance was independently associated with NASH and Ruminococcus with F≥2 fibrosis. Stratification according to the abundance of these two bacteria generated three patient subgroups with increasing severity of NAFLD lesions. Based on imputed metagenomic profiles, Kyoto Encyclopedia of Genes and Genomes pathways significantly related to NASH and fibrosis F≥2 were mostly related to carbohydrate, lipid, and amino acid metabolism. Conclusion: NAFLD severity associates with gut dysbiosis and a shift in metabolic function of the gut microbiota. We identified Bacteroides as independently associated with NASH and Ruminococcus with significant fibrosis. Thus, gut microbiota analysis adds information to classical predictors of NAFLD severity and suggests novel metabolic targets for pre‐/probiotics therapies. (Hepatology 2016;63:764–775)
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However, data about gut dysbiosis in human NAFLD remain scarce in the literature, especially studies including the whole spectrum of NAFLD lesions. We aimed to evaluate the association between gut dysbiosis and severe NAFLD lesions, that is, nonalcoholic steatohepatitis (NASH) and fibrosis, in a well‐characterized population of adult NAFLD. Fifty‐seven patients with biopsy‐proven NAFLD were enrolled. Taxonomic composition of gut microbiota was determined using 16S ribosomal RNA gene sequencing of stool samples. Thirty patients had F0/F1 fibrosis stage at liver biopsy (10 with NASH), and 27 patients had significant F≥2 fibrosis (25 with NASH). Bacteroides abundance was significantly increased in NASH and F≥2 patients, whereas Prevotella abundance was decreased. Ruminococcus abundance was significantly higher in F≥2 patients. By multivariate analysis, Bacteroides abundance was independently associated with NASH and Ruminococcus with F≥2 fibrosis. Stratification according to the abundance of these two bacteria generated three patient subgroups with increasing severity of NAFLD lesions. Based on imputed metagenomic profiles, Kyoto Encyclopedia of Genes and Genomes pathways significantly related to NASH and fibrosis F≥2 were mostly related to carbohydrate, lipid, and amino acid metabolism. Conclusion: NAFLD severity associates with gut dysbiosis and a shift in metabolic function of the gut microbiota. We identified Bacteroides as independently associated with NASH and Ruminococcus with significant fibrosis. Thus, gut microbiota analysis adds information to classical predictors of NAFLD severity and suggests novel metabolic targets for pre‐/probiotics therapies. 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Stratification according to the abundance of these two bacteria generated three patient subgroups with increasing severity of NAFLD lesions. Based on imputed metagenomic profiles, Kyoto Encyclopedia of Genes and Genomes pathways significantly related to NASH and fibrosis F≥2 were mostly related to carbohydrate, lipid, and amino acid metabolism. Conclusion: NAFLD severity associates with gut dysbiosis and a shift in metabolic function of the gut microbiota. We identified Bacteroides as independently associated with NASH and Ruminococcus with significant fibrosis. Thus, gut microbiota analysis adds information to classical predictors of NAFLD severity and suggests novel metabolic targets for pre‐/probiotics therapies. 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Mueller, Olaf ; Barret, Matthieu ; Machado, Mariana ; Fizanne, Lionel ; Araujo‐Perez, Felix ; Guy, Cynthia D. ; Seed, Patrick C. ; Rawls, John F. ; David, Lawrence A. ; Hunault, Gilles ; Oberti, Frédéric ; Calès, Paul ; Diehl, Anna Mae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4836-b95a84f91f6c8e54eb8b1c162e8bd109edc40c74cf44ae9247bf74b7b048bcec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Abundance</topic><topic>Aged</topic><topic>Amino acids</topic><topic>Bacteroides</topic><topic>Biopsy</topic><topic>Dysbacteriosis</topic><topic>Dysbiosis - complications</topic><topic>Dysbiosis - microbiology</topic><topic>Fatty liver</topic><topic>Feces - microbiology</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Gastrointestinal Microbiome</topic><topic>Genomes</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Intestinal microflora</topic><topic>Life Sciences</topic><topic>Lipid metabolism</topic><topic>Liver - pathology</topic><topic>Liver diseases</topic><topic>Male</topic><topic>Metabolism</topic><topic>Metagenome</topic><topic>Microbiota</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Non-alcoholic Fatty Liver Disease - complications</topic><topic>Non-alcoholic Fatty Liver Disease - microbiology</topic><topic>Non-alcoholic Fatty Liver Disease - pathology</topic><topic>Prevotella</topic><topic>Probiotics</topic><topic>rRNA 16S</topic><topic>Ruminococcus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boursier, Jérôme</creatorcontrib><creatorcontrib>Mueller, Olaf</creatorcontrib><creatorcontrib>Barret, Matthieu</creatorcontrib><creatorcontrib>Machado, Mariana</creatorcontrib><creatorcontrib>Fizanne, Lionel</creatorcontrib><creatorcontrib>Araujo‐Perez, Felix</creatorcontrib><creatorcontrib>Guy, Cynthia D.</creatorcontrib><creatorcontrib>Seed, Patrick C.</creatorcontrib><creatorcontrib>Rawls, John F.</creatorcontrib><creatorcontrib>David, Lawrence A.</creatorcontrib><creatorcontrib>Hunault, Gilles</creatorcontrib><creatorcontrib>Oberti, Frédéric</creatorcontrib><creatorcontrib>Calès, Paul</creatorcontrib><creatorcontrib>Diehl, Anna Mae</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; 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Stratification according to the abundance of these two bacteria generated three patient subgroups with increasing severity of NAFLD lesions. Based on imputed metagenomic profiles, Kyoto Encyclopedia of Genes and Genomes pathways significantly related to NASH and fibrosis F≥2 were mostly related to carbohydrate, lipid, and amino acid metabolism. Conclusion: NAFLD severity associates with gut dysbiosis and a shift in metabolic function of the gut microbiota. We identified Bacteroides as independently associated with NASH and Ruminococcus with significant fibrosis. Thus, gut microbiota analysis adds information to classical predictors of NAFLD severity and suggests novel metabolic targets for pre‐/probiotics therapies. 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subjects Abundance
Aged
Amino acids
Bacteroides
Biopsy
Dysbacteriosis
Dysbiosis - complications
Dysbiosis - microbiology
Fatty liver
Feces - microbiology
Female
Fibrosis
Gastrointestinal Microbiome
Genomes
Hepatology
Humans
Intestinal microflora
Life Sciences
Lipid metabolism
Liver - pathology
Liver diseases
Male
Metabolism
Metagenome
Microbiota
Middle Aged
Multivariate analysis
Non-alcoholic Fatty Liver Disease - complications
Non-alcoholic Fatty Liver Disease - microbiology
Non-alcoholic Fatty Liver Disease - pathology
Prevotella
Probiotics
rRNA 16S
Ruminococcus
title The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota
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