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Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation
The gut microbiota is emerging as an important modulator of neurodegenerative diseases, and accumulating evidence has linked gut microbes to Parkinson’s disease (PD) symptomatology and pathophysiology. PD is often preceded by gastrointestinal symptoms and alterations of the enteric nervous system ac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946946/ https://www.ncbi.nlm.nih.gov/pubmed/33692356 http://dx.doi.org/10.1038/s41531-021-00156-z |
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author | Romano, Stefano Savva, George M. Bedarf, Janis R. Charles, Ian G. Hildebrand, Falk Narbad, Arjan |
author_facet | Romano, Stefano Savva, George M. Bedarf, Janis R. Charles, Ian G. Hildebrand, Falk Narbad, Arjan |
author_sort | Romano, Stefano |
collection | PubMed |
description | The gut microbiota is emerging as an important modulator of neurodegenerative diseases, and accumulating evidence has linked gut microbes to Parkinson’s disease (PD) symptomatology and pathophysiology. PD is often preceded by gastrointestinal symptoms and alterations of the enteric nervous system accompany the disease. Several studies have analyzed the gut microbiome in PD, but a consensus on the features of the PD-specific microbiota is missing. Here, we conduct a meta-analysis re-analyzing the ten currently available 16S microbiome datasets to investigate whether common alterations in the gut microbiota of PD patients exist across cohorts. We found significant alterations in the PD-associated microbiome, which are robust to study-specific technical heterogeneities, although differences in microbiome structure between PD and controls are small. Enrichment of the genera Lactobacillus, Akkermansia, and Bifidobacterium and depletion of bacteria belonging to the Lachnospiraceae family and the Faecalibacterium genus, both important short-chain fatty acids producers, emerged as the most consistent PD gut microbiome alterations. This dysbiosis might result in a pro-inflammatory status which could be linked to the recurrent gastrointestinal symptoms affecting PD patients. |
format | Online Article Text |
id | pubmed-7946946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79469462021-03-28 Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation Romano, Stefano Savva, George M. Bedarf, Janis R. Charles, Ian G. Hildebrand, Falk Narbad, Arjan NPJ Parkinsons Dis Article The gut microbiota is emerging as an important modulator of neurodegenerative diseases, and accumulating evidence has linked gut microbes to Parkinson’s disease (PD) symptomatology and pathophysiology. PD is often preceded by gastrointestinal symptoms and alterations of the enteric nervous system accompany the disease. Several studies have analyzed the gut microbiome in PD, but a consensus on the features of the PD-specific microbiota is missing. Here, we conduct a meta-analysis re-analyzing the ten currently available 16S microbiome datasets to investigate whether common alterations in the gut microbiota of PD patients exist across cohorts. We found significant alterations in the PD-associated microbiome, which are robust to study-specific technical heterogeneities, although differences in microbiome structure between PD and controls are small. Enrichment of the genera Lactobacillus, Akkermansia, and Bifidobacterium and depletion of bacteria belonging to the Lachnospiraceae family and the Faecalibacterium genus, both important short-chain fatty acids producers, emerged as the most consistent PD gut microbiome alterations. This dysbiosis might result in a pro-inflammatory status which could be linked to the recurrent gastrointestinal symptoms affecting PD patients. Nature Publishing Group UK 2021-03-10 /pmc/articles/PMC7946946/ /pubmed/33692356 http://dx.doi.org/10.1038/s41531-021-00156-z Text en © The Author(s) 2021 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 Romano, Stefano Savva, George M. Bedarf, Janis R. Charles, Ian G. Hildebrand, Falk Narbad, Arjan Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation |
title | Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation |
title_full | Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation |
title_fullStr | Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation |
title_full_unstemmed | Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation |
title_short | Meta-analysis of the Parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation |
title_sort | meta-analysis of the parkinson’s disease gut microbiome suggests alterations linked to intestinal inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946946/ https://www.ncbi.nlm.nih.gov/pubmed/33692356 http://dx.doi.org/10.1038/s41531-021-00156-z |
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