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The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis

Patients with Parkinson's disease (PD) were often observed with gastrointestinal symptoms, which preceded the onset of motor symptoms. Neuropathology of PD has also been found in the enteric nervous system (ENS). Many studies have reported significant PD-related alterations of gut microbiota. T...

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Autores principales: Shen, Ting, Yue, Yumei, He, Tingting, Huang, Cong, Qu, Boyi, Lv, Wen, Lai, Hsin-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907649/
https://www.ncbi.nlm.nih.gov/pubmed/33643026
http://dx.doi.org/10.3389/fnagi.2021.636545
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author Shen, Ting
Yue, Yumei
He, Tingting
Huang, Cong
Qu, Boyi
Lv, Wen
Lai, Hsin-Yi
author_facet Shen, Ting
Yue, Yumei
He, Tingting
Huang, Cong
Qu, Boyi
Lv, Wen
Lai, Hsin-Yi
author_sort Shen, Ting
collection PubMed
description Patients with Parkinson's disease (PD) were often observed with gastrointestinal symptoms, which preceded the onset of motor symptoms. Neuropathology of PD has also been found in the enteric nervous system (ENS). Many studies have reported significant PD-related alterations of gut microbiota. This meta-analysis was performed to evaluate the differences of gut microbiota between patients with PD and healthy controls (HCs) across different geographical regions. We conducted a systematic online search for case-control studies detecting gut microbiota in patients with PD and HCs. Mean difference (MD) and 95% confidence interval (CI) were calculated to access alterations in the abundance of certain microbiota families in PD. Fifteen case-control studies were included in this meta-analysis study. Our results showed significant lower abundance levels of Prevotellaceae (MD = −0.37, 95% CI = −0.62 to −0.11), Faecalibacterium (MD = −0.41, 95% CI: −0.57 to −0.24), and Lachnospiraceae (MD = −0.34, 95% CI = −0.59 to −0.09) in patients with PD compared to HCs. Significant higher abundance level of Bifidobacteriaceae (MD = 0.38, 95%; CI = 0.12 to 0.63), Ruminococcaceae (MD = 0.58, 95% CI = 0.07 to 1.10), Verrucomicrobiaceae (MD = 0.45, 95% CI = 0.21 to 0.69), and Christensenellaceae (MD = 0.20, 95% CI = 0.07 to 0.34) was also found in patients with PD. Thus, shared alterations of certain gut microbiota were detected in patients with PD across different geographical regions. These PD-related gut microbiota dysbiosis might lead to the impairment of short-chain fatty acids (SCFAs) producing process, lipid metabolism, immunoregulatory function, and intestinal permeability, which contribute to the pathogenesis of PD.
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spelling pubmed-79076492021-02-27 The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis Shen, Ting Yue, Yumei He, Tingting Huang, Cong Qu, Boyi Lv, Wen Lai, Hsin-Yi Front Aging Neurosci Neuroscience Patients with Parkinson's disease (PD) were often observed with gastrointestinal symptoms, which preceded the onset of motor symptoms. Neuropathology of PD has also been found in the enteric nervous system (ENS). Many studies have reported significant PD-related alterations of gut microbiota. This meta-analysis was performed to evaluate the differences of gut microbiota between patients with PD and healthy controls (HCs) across different geographical regions. We conducted a systematic online search for case-control studies detecting gut microbiota in patients with PD and HCs. Mean difference (MD) and 95% confidence interval (CI) were calculated to access alterations in the abundance of certain microbiota families in PD. Fifteen case-control studies were included in this meta-analysis study. Our results showed significant lower abundance levels of Prevotellaceae (MD = −0.37, 95% CI = −0.62 to −0.11), Faecalibacterium (MD = −0.41, 95% CI: −0.57 to −0.24), and Lachnospiraceae (MD = −0.34, 95% CI = −0.59 to −0.09) in patients with PD compared to HCs. Significant higher abundance level of Bifidobacteriaceae (MD = 0.38, 95%; CI = 0.12 to 0.63), Ruminococcaceae (MD = 0.58, 95% CI = 0.07 to 1.10), Verrucomicrobiaceae (MD = 0.45, 95% CI = 0.21 to 0.69), and Christensenellaceae (MD = 0.20, 95% CI = 0.07 to 0.34) was also found in patients with PD. Thus, shared alterations of certain gut microbiota were detected in patients with PD across different geographical regions. These PD-related gut microbiota dysbiosis might lead to the impairment of short-chain fatty acids (SCFAs) producing process, lipid metabolism, immunoregulatory function, and intestinal permeability, which contribute to the pathogenesis of PD. Frontiers Media S.A. 2021-02-12 /pmc/articles/PMC7907649/ /pubmed/33643026 http://dx.doi.org/10.3389/fnagi.2021.636545 Text en Copyright © 2021 Shen, Yue, He, Huang, Qu, Lv and Lai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Shen, Ting
Yue, Yumei
He, Tingting
Huang, Cong
Qu, Boyi
Lv, Wen
Lai, Hsin-Yi
The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis
title The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis
title_full The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis
title_fullStr The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis
title_full_unstemmed The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis
title_short The Association Between the Gut Microbiota and Parkinson's Disease, a Meta-Analysis
title_sort association between the gut microbiota and parkinson's disease, a meta-analysis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907649/
https://www.ncbi.nlm.nih.gov/pubmed/33643026
http://dx.doi.org/10.3389/fnagi.2021.636545
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