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Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis

The interaction of gut microbiota, related metabolites and inflammation factors with nonalcoholic fatty liver disease (NAFLD) remains unclearly defined. The aim of this systematic review and meta-analysis was to synthesize previous study findings to better understand this interaction. Relevant resea...

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Autores principales: Pan, Xiongfeng, Wen, Shi Wu, Kaminga, Atipatsa C., Liu, Aizhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264254/
https://www.ncbi.nlm.nih.gov/pubmed/32483129
http://dx.doi.org/10.1038/s41598-020-65051-8
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author Pan, Xiongfeng
Wen, Shi Wu
Kaminga, Atipatsa C.
Liu, Aizhong
author_facet Pan, Xiongfeng
Wen, Shi Wu
Kaminga, Atipatsa C.
Liu, Aizhong
author_sort Pan, Xiongfeng
collection PubMed
description The interaction of gut microbiota, related metabolites and inflammation factors with nonalcoholic fatty liver disease (NAFLD) remains unclearly defined. The aim of this systematic review and meta-analysis was to synthesize previous study findings to better understand this interaction. Relevant research articles published not later than September, 2019 were searched in the following databases: Web of Science, PubMed, Embase, and Cochrane Library. The search strategy and inclusion criteria for this study yielded a total of 47 studies, of which only 11 were eligible for meta-analysis. The narrative analysis of these articles found that there is interplay between the key gut microbiota, related metabolites and inflammation factors, which modulate the development and progression of NAFLD. In addition, the results of meta-analysis showed that probiotic supplementation significantly decreased tumor necrosis factor-α (TNF-α) in NAFLD patients (standardized mean difference (SMD) = −0.52, confidence interval (CI): −0.86 to −0.18, and p = 0.003) and C-reactive protein (CRP) (SMD = −0.62, CI: −0.80 to −0.43, and p < 0.001). However, whether therapies can target TNF-α and CRP in order treat NAFLD still needs further investigation. Therefore, these results suggest that the interaction of the key gut microbiota, related metabolites and inflammation factors with NAFLD may provide a novel therapeutic target for the clinical and pharmacological treatment of NAFLD.
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spelling pubmed-72642542020-06-05 Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis Pan, Xiongfeng Wen, Shi Wu Kaminga, Atipatsa C. Liu, Aizhong Sci Rep Article The interaction of gut microbiota, related metabolites and inflammation factors with nonalcoholic fatty liver disease (NAFLD) remains unclearly defined. The aim of this systematic review and meta-analysis was to synthesize previous study findings to better understand this interaction. Relevant research articles published not later than September, 2019 were searched in the following databases: Web of Science, PubMed, Embase, and Cochrane Library. The search strategy and inclusion criteria for this study yielded a total of 47 studies, of which only 11 were eligible for meta-analysis. The narrative analysis of these articles found that there is interplay between the key gut microbiota, related metabolites and inflammation factors, which modulate the development and progression of NAFLD. In addition, the results of meta-analysis showed that probiotic supplementation significantly decreased tumor necrosis factor-α (TNF-α) in NAFLD patients (standardized mean difference (SMD) = −0.52, confidence interval (CI): −0.86 to −0.18, and p = 0.003) and C-reactive protein (CRP) (SMD = −0.62, CI: −0.80 to −0.43, and p < 0.001). However, whether therapies can target TNF-α and CRP in order treat NAFLD still needs further investigation. Therefore, these results suggest that the interaction of the key gut microbiota, related metabolites and inflammation factors with NAFLD may provide a novel therapeutic target for the clinical and pharmacological treatment of NAFLD. Nature Publishing Group UK 2020-06-01 /pmc/articles/PMC7264254/ /pubmed/32483129 http://dx.doi.org/10.1038/s41598-020-65051-8 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pan, Xiongfeng
Wen, Shi Wu
Kaminga, Atipatsa C.
Liu, Aizhong
Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis
title Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis
title_full Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis
title_fullStr Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis
title_full_unstemmed Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis
title_short Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis
title_sort gut metabolites and inflammation factors in non-alcoholic fatty liver disease: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264254/
https://www.ncbi.nlm.nih.gov/pubmed/32483129
http://dx.doi.org/10.1038/s41598-020-65051-8
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