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Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study
Recently, cognitive impairments (CI) and behavioral abnormalities in patients with amyotrophic lateral sclerosis (ALS) have been reported. However, the underlying mechanisms have been poorly understood. In the current study, we explored the role of gut microbiota in CI of ALS patients. We collected...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial Department of Journal of Biomedical Research
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018415/ https://www.ncbi.nlm.nih.gov/pubmed/36814376 http://dx.doi.org/10.7555/JBR.36.20220198 |
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author | Gong, Zhenxiang Ba, Li Tang, Jiahui Yang, Yuan Li, Zehui Liu, Mao Yang, Chun Ding, Fengfei Zhang, Min |
author_facet | Gong, Zhenxiang Ba, Li Tang, Jiahui Yang, Yuan Li, Zehui Liu, Mao Yang, Chun Ding, Fengfei Zhang, Min |
author_sort | Gong, Zhenxiang |
collection | PubMed |
description | Recently, cognitive impairments (CI) and behavioral abnormalities in patients with amyotrophic lateral sclerosis (ALS) have been reported. However, the underlying mechanisms have been poorly understood. In the current study, we explored the role of gut microbiota in CI of ALS patients. We collected fecal samples from 35 ALS patients and 35 healthy controls. The cognitive function of the ALS patients was evaluated using the Edinburgh Cognitive and Behavioral ALS Screen. We analyzed these samples by using 16S rRNA gene sequencing as well as both untargeted and targeted (bile acids) metabolite mapping between patients with CI and patients with normal cognition (CN). We found altered gut microbial communities and a lower ratio of Firmicutes/Bacteroidetes in the CI group, compared with the CN group. In addition, the untargeted metabolite mapping revealed that 26 and 17 metabolites significantly increased and decreased, respectively, in the CI group, compared with the CN group. These metabolites were mapped to the metabolic pathways associated with bile acids. We further found that cholic acid and chenodeoxycholic acid were significantly lower in the CI group than in the CN group. In conclusion, we found that the gut microbiota and its metabolome profile differed between ALS patients with and without CI and that the altered bile acid profile in fecal samples was significantly associated with CI in ALS patients. These results need to be replicated in larger studies in the future. |
format | Online Article Text |
id | pubmed-10018415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Editorial Department of Journal of Biomedical Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-100184152023-03-17 Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study Gong, Zhenxiang Ba, Li Tang, Jiahui Yang, Yuan Li, Zehui Liu, Mao Yang, Chun Ding, Fengfei Zhang, Min J Biomed Res Original Article Recently, cognitive impairments (CI) and behavioral abnormalities in patients with amyotrophic lateral sclerosis (ALS) have been reported. However, the underlying mechanisms have been poorly understood. In the current study, we explored the role of gut microbiota in CI of ALS patients. We collected fecal samples from 35 ALS patients and 35 healthy controls. The cognitive function of the ALS patients was evaluated using the Edinburgh Cognitive and Behavioral ALS Screen. We analyzed these samples by using 16S rRNA gene sequencing as well as both untargeted and targeted (bile acids) metabolite mapping between patients with CI and patients with normal cognition (CN). We found altered gut microbial communities and a lower ratio of Firmicutes/Bacteroidetes in the CI group, compared with the CN group. In addition, the untargeted metabolite mapping revealed that 26 and 17 metabolites significantly increased and decreased, respectively, in the CI group, compared with the CN group. These metabolites were mapped to the metabolic pathways associated with bile acids. We further found that cholic acid and chenodeoxycholic acid were significantly lower in the CI group than in the CN group. In conclusion, we found that the gut microbiota and its metabolome profile differed between ALS patients with and without CI and that the altered bile acid profile in fecal samples was significantly associated with CI in ALS patients. These results need to be replicated in larger studies in the future. Editorial Department of Journal of Biomedical Research 2023-03 2022-12-28 /pmc/articles/PMC10018415/ /pubmed/36814376 http://dx.doi.org/10.7555/JBR.36.20220198 Text en Copyright and License information: Journal of Biomedical Research, CAS Springer-Verlag Berlin Heidelberg 2023 https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Gong, Zhenxiang Ba, Li Tang, Jiahui Yang, Yuan Li, Zehui Liu, Mao Yang, Chun Ding, Fengfei Zhang, Min Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study |
title | Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study |
title_full | Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study |
title_fullStr | Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study |
title_full_unstemmed | Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study |
title_short | Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study |
title_sort | gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: a multi-omics study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018415/ https://www.ncbi.nlm.nih.gov/pubmed/36814376 http://dx.doi.org/10.7555/JBR.36.20220198 |
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