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Gut microbiota in dementia with Lewy bodies
Gut microbiota and fecal bile acids were analyzed in 278 patients with α-synucleinopathies, which were comprised of 28 patients with dementia with Lewy bodies (DLB), 224 patients with Parkinson’s disease (PD), and 26 patients with idiopathic rapid eye movement sleep behavior disorder (iRBD). Similar...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734655/ https://www.ncbi.nlm.nih.gov/pubmed/36494405 http://dx.doi.org/10.1038/s41531-022-00428-2 |
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author | Nishiwaki, Hiroshi Ueyama, Jun Kashihara, Kenichi Ito, Mikako Hamaguchi, Tomonari Maeda, Tetsuya Tsuboi, Yoshio Katsuno, Masahisa Hirayama, Masaaki Ohno, Kinji |
author_facet | Nishiwaki, Hiroshi Ueyama, Jun Kashihara, Kenichi Ito, Mikako Hamaguchi, Tomonari Maeda, Tetsuya Tsuboi, Yoshio Katsuno, Masahisa Hirayama, Masaaki Ohno, Kinji |
author_sort | Nishiwaki, Hiroshi |
collection | PubMed |
description | Gut microbiota and fecal bile acids were analyzed in 278 patients with α-synucleinopathies, which were comprised of 28 patients with dementia with Lewy bodies (DLB), 224 patients with Parkinson’s disease (PD), and 26 patients with idiopathic rapid eye movement sleep behavior disorder (iRBD). Similarly to PD, short-chain fatty acids-producing genera were decreased in DLB. Additionally, Ruminococcus torques and Collinsella were increased in DLB, which were not changed in PD. Random forest models to differentiate DLB and PD showed that high Ruminococcus torques and high Collinsella, which presumably increase intestinal permeability, as well as low Bifidobacterium, which are also observed in Alzheimer’s disease, were predictive of DLB. As Ruminococcus torques and Collinsella are also major secondary bile acids-producing bacteria, we quantified fecal bile acids and found that the production of ursodeoxycholic acid (UDCA) was high in DLB. Increased UDCA in DLB may mitigate neuroinflammation at the substantia nigra, whereas neuroinflammation may not be critical at the neocortex. Theraeutic intervention to increase Bifidobacteirum and its metabolites may retard the development and progression of DLB. |
format | Online Article Text |
id | pubmed-9734655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97346552022-12-11 Gut microbiota in dementia with Lewy bodies Nishiwaki, Hiroshi Ueyama, Jun Kashihara, Kenichi Ito, Mikako Hamaguchi, Tomonari Maeda, Tetsuya Tsuboi, Yoshio Katsuno, Masahisa Hirayama, Masaaki Ohno, Kinji NPJ Parkinsons Dis Article Gut microbiota and fecal bile acids were analyzed in 278 patients with α-synucleinopathies, which were comprised of 28 patients with dementia with Lewy bodies (DLB), 224 patients with Parkinson’s disease (PD), and 26 patients with idiopathic rapid eye movement sleep behavior disorder (iRBD). Similarly to PD, short-chain fatty acids-producing genera were decreased in DLB. Additionally, Ruminococcus torques and Collinsella were increased in DLB, which were not changed in PD. Random forest models to differentiate DLB and PD showed that high Ruminococcus torques and high Collinsella, which presumably increase intestinal permeability, as well as low Bifidobacterium, which are also observed in Alzheimer’s disease, were predictive of DLB. As Ruminococcus torques and Collinsella are also major secondary bile acids-producing bacteria, we quantified fecal bile acids and found that the production of ursodeoxycholic acid (UDCA) was high in DLB. Increased UDCA in DLB may mitigate neuroinflammation at the substantia nigra, whereas neuroinflammation may not be critical at the neocortex. Theraeutic intervention to increase Bifidobacteirum and its metabolites may retard the development and progression of DLB. Nature Publishing Group UK 2022-12-09 /pmc/articles/PMC9734655/ /pubmed/36494405 http://dx.doi.org/10.1038/s41531-022-00428-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Nishiwaki, Hiroshi Ueyama, Jun Kashihara, Kenichi Ito, Mikako Hamaguchi, Tomonari Maeda, Tetsuya Tsuboi, Yoshio Katsuno, Masahisa Hirayama, Masaaki Ohno, Kinji Gut microbiota in dementia with Lewy bodies |
title | Gut microbiota in dementia with Lewy bodies |
title_full | Gut microbiota in dementia with Lewy bodies |
title_fullStr | Gut microbiota in dementia with Lewy bodies |
title_full_unstemmed | Gut microbiota in dementia with Lewy bodies |
title_short | Gut microbiota in dementia with Lewy bodies |
title_sort | gut microbiota in dementia with lewy bodies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734655/ https://www.ncbi.nlm.nih.gov/pubmed/36494405 http://dx.doi.org/10.1038/s41531-022-00428-2 |
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