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Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction
BACKGROUND: Schizophrenia (SCZ) is a heterogeneous neuropsychiatric disorder for which current treatment has insufficient efficacy and severe adverse effects. The modifiable gut microbiome might be a potential target for intervention to improve neurobiological functions through the gut-microbiome-br...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140391/ https://www.ncbi.nlm.nih.gov/pubmed/37124355 http://dx.doi.org/10.1016/j.bpsgos.2022.01.009 |
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author | Thirion, Florence Speyer, Helene Hansen, Tue Haldor Nielsen, Trine Fan, Yong Le Chatelier, Emmanuelle Fromentin, Sébastien Berland, Magali Plaza Oñate, Florian Pons, Nicolas Galleron, Nathalie Levenez, Florence Markó, Lajos Birkner, Till Jørgensen, Torben Forslund, Sofia K. Vestergaard, Henrik Hansen, Torben Nordentoft, Merete Mors, Ole Benros, Michael E. Pedersen, Oluf Ehrlich, Stanislav D. |
author_facet | Thirion, Florence Speyer, Helene Hansen, Tue Haldor Nielsen, Trine Fan, Yong Le Chatelier, Emmanuelle Fromentin, Sébastien Berland, Magali Plaza Oñate, Florian Pons, Nicolas Galleron, Nathalie Levenez, Florence Markó, Lajos Birkner, Till Jørgensen, Torben Forslund, Sofia K. Vestergaard, Henrik Hansen, Torben Nordentoft, Merete Mors, Ole Benros, Michael E. Pedersen, Oluf Ehrlich, Stanislav D. |
author_sort | Thirion, Florence |
collection | PubMed |
description | BACKGROUND: Schizophrenia (SCZ) is a heterogeneous neuropsychiatric disorder for which current treatment has insufficient efficacy and severe adverse effects. The modifiable gut microbiome might be a potential target for intervention to improve neurobiological functions through the gut-microbiome-brain axis. METHODS: In this case-control study, gut microbiota of 132 patients with SCZ and increased waist circumference were compared with gut microbiota of two age- and sex-matched control groups, composed of 132 healthy individuals and 132 individuals with metabolic syndrome. Shotgun sequencing was used to characterize fecal samples at the taxonomic and functional levels. Cognition of the patients with SCZ was evaluated using the Brief Assessment of Cognition instrument. RESULTS: SCZ gut microbiota differed significantly from those of healthy control subjects and individuals with metabolic syndrome in terms of richness and global composition. SCZ gut microbiota were notably enriched in Flavonifractor plautii, Collinsella aerofaciens, Bilophila wadsworthia, and Sellimonas intestinalis, while depleted in Faecalibacterium prausnitzii, Ruminococcus lactaris, Ruminococcus bicirculans, and Veillonella rogosae. Functional potential of the gut microbiota accounted for 11% of cognition variability. In particular, the bacterial functional module for synthesizing tyrosine, a precursor for dopamine, was in SCZ cases positively associated with cognitive score (ρ = 0.34, q ≤ .1). CONCLUSIONS: Overall, this study shows that the gut microbiome of patients with SCZ differs greatly from that of healthy control subjects or individuals with metabolic syndrome. Cognitive function of patients with SCZ is associated with the potential for gut bacterial biosynthesis of tyrosine, a precursor for dopamine, suggesting that gut microbiota might be an intervention target for alleviation of cognitive dysfunction in SCZ. |
format | Online Article Text |
id | pubmed-10140391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101403912023-04-29 Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction Thirion, Florence Speyer, Helene Hansen, Tue Haldor Nielsen, Trine Fan, Yong Le Chatelier, Emmanuelle Fromentin, Sébastien Berland, Magali Plaza Oñate, Florian Pons, Nicolas Galleron, Nathalie Levenez, Florence Markó, Lajos Birkner, Till Jørgensen, Torben Forslund, Sofia K. Vestergaard, Henrik Hansen, Torben Nordentoft, Merete Mors, Ole Benros, Michael E. Pedersen, Oluf Ehrlich, Stanislav D. Biol Psychiatry Glob Open Sci Archival Report BACKGROUND: Schizophrenia (SCZ) is a heterogeneous neuropsychiatric disorder for which current treatment has insufficient efficacy and severe adverse effects. The modifiable gut microbiome might be a potential target for intervention to improve neurobiological functions through the gut-microbiome-brain axis. METHODS: In this case-control study, gut microbiota of 132 patients with SCZ and increased waist circumference were compared with gut microbiota of two age- and sex-matched control groups, composed of 132 healthy individuals and 132 individuals with metabolic syndrome. Shotgun sequencing was used to characterize fecal samples at the taxonomic and functional levels. Cognition of the patients with SCZ was evaluated using the Brief Assessment of Cognition instrument. RESULTS: SCZ gut microbiota differed significantly from those of healthy control subjects and individuals with metabolic syndrome in terms of richness and global composition. SCZ gut microbiota were notably enriched in Flavonifractor plautii, Collinsella aerofaciens, Bilophila wadsworthia, and Sellimonas intestinalis, while depleted in Faecalibacterium prausnitzii, Ruminococcus lactaris, Ruminococcus bicirculans, and Veillonella rogosae. Functional potential of the gut microbiota accounted for 11% of cognition variability. In particular, the bacterial functional module for synthesizing tyrosine, a precursor for dopamine, was in SCZ cases positively associated with cognitive score (ρ = 0.34, q ≤ .1). CONCLUSIONS: Overall, this study shows that the gut microbiome of patients with SCZ differs greatly from that of healthy control subjects or individuals with metabolic syndrome. Cognitive function of patients with SCZ is associated with the potential for gut bacterial biosynthesis of tyrosine, a precursor for dopamine, suggesting that gut microbiota might be an intervention target for alleviation of cognitive dysfunction in SCZ. Elsevier 2022-02-10 /pmc/articles/PMC10140391/ /pubmed/37124355 http://dx.doi.org/10.1016/j.bpsgos.2022.01.009 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Archival Report Thirion, Florence Speyer, Helene Hansen, Tue Haldor Nielsen, Trine Fan, Yong Le Chatelier, Emmanuelle Fromentin, Sébastien Berland, Magali Plaza Oñate, Florian Pons, Nicolas Galleron, Nathalie Levenez, Florence Markó, Lajos Birkner, Till Jørgensen, Torben Forslund, Sofia K. Vestergaard, Henrik Hansen, Torben Nordentoft, Merete Mors, Ole Benros, Michael E. Pedersen, Oluf Ehrlich, Stanislav D. Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction |
title | Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction |
title_full | Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction |
title_fullStr | Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction |
title_full_unstemmed | Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction |
title_short | Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction |
title_sort | alteration of gut microbiome in patients with schizophrenia indicates links between bacterial tyrosine biosynthesis and cognitive dysfunction |
topic | Archival Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140391/ https://www.ncbi.nlm.nih.gov/pubmed/37124355 http://dx.doi.org/10.1016/j.bpsgos.2022.01.009 |
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