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Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood

INTRODUCTION: Gut microbial disturbance has been established as potential pathogenesis of mental disorders. However, the signatures and differences regarding patients with schizophrenia (SCH) or bipolar disorder (BD) in emerging adulthood as well as their subtypes have been poorly addressed. METHODS...

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Autores principales: Chen, Yi‐huan, Zhou, Cui‐hong, Yu, Huan, Wu, Wen‐jun, Wang, Ying‐wei, Liu, Ling, Hu, Guang‐tao, Li, Bao‐juan, Peng, Zheng‐wu, Wang, Hua‐ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314106/
https://www.ncbi.nlm.nih.gov/pubmed/36468448
http://dx.doi.org/10.1111/cns.14044
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author Chen, Yi‐huan
Zhou, Cui‐hong
Yu, Huan
Wu, Wen‐jun
Wang, Ying‐wei
Liu, Ling
Hu, Guang‐tao
Li, Bao‐juan
Peng, Zheng‐wu
Wang, Hua‐ning
author_facet Chen, Yi‐huan
Zhou, Cui‐hong
Yu, Huan
Wu, Wen‐jun
Wang, Ying‐wei
Liu, Ling
Hu, Guang‐tao
Li, Bao‐juan
Peng, Zheng‐wu
Wang, Hua‐ning
author_sort Chen, Yi‐huan
collection PubMed
description INTRODUCTION: Gut microbial disturbance has been established as potential pathogenesis of mental disorders. However, the signatures and differences regarding patients with schizophrenia (SCH) or bipolar disorder (BD) in emerging adulthood as well as their subtypes have been poorly addressed. METHODS: In the present study, stool samples obtained from 63 emerging adult patients with schizophrenia (SCH), 50 with bipolar disorder (BD), and 40 healthy controls (HC) were analyzed by 16 S rRNA gene sequencing; psychiatric symptoms and psychological, social, and professional functioning were also assessed. RESULTS: We found that gut microbiota composition was remarkably changed in the patients with SCH and BD. Moreover, the distinct gut microbiome signatures and their potential function in bipolar depression (BP‐D) and SCH with predominantly negative symptoms (SCH‐N) as well as bipolar mania (BP‐M) and SCH with predominantly positive symptoms (SCH‐P) were also observed. Furthermore, we identified diagnostic potential biomarkers that can distinguish BD from HC (38 genera, AUC = 0.961), SCH from HC (32 genera, AUC = 0.962), and BD from Scheme (13 genera, AUC = 0.823). Potential diagnostic biomarkers that can distinguish BD‐D from SCH‐N (16 genera, AUC = 0.969) and BD‐M from SCH‐P (31 genera, AUC = 0.938) were also identified. CONCLUSION: This study provides further understanding of abnormal gut microbiome in emerging adulthood patients with SCH and BD and lay the potential foundation for the development of microbe‐based clinical diagnosis for BD and SCH.
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spelling pubmed-103141062023-07-02 Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood Chen, Yi‐huan Zhou, Cui‐hong Yu, Huan Wu, Wen‐jun Wang, Ying‐wei Liu, Ling Hu, Guang‐tao Li, Bao‐juan Peng, Zheng‐wu Wang, Hua‐ning CNS Neurosci Ther Original Articles INTRODUCTION: Gut microbial disturbance has been established as potential pathogenesis of mental disorders. However, the signatures and differences regarding patients with schizophrenia (SCH) or bipolar disorder (BD) in emerging adulthood as well as their subtypes have been poorly addressed. METHODS: In the present study, stool samples obtained from 63 emerging adult patients with schizophrenia (SCH), 50 with bipolar disorder (BD), and 40 healthy controls (HC) were analyzed by 16 S rRNA gene sequencing; psychiatric symptoms and psychological, social, and professional functioning were also assessed. RESULTS: We found that gut microbiota composition was remarkably changed in the patients with SCH and BD. Moreover, the distinct gut microbiome signatures and their potential function in bipolar depression (BP‐D) and SCH with predominantly negative symptoms (SCH‐N) as well as bipolar mania (BP‐M) and SCH with predominantly positive symptoms (SCH‐P) were also observed. Furthermore, we identified diagnostic potential biomarkers that can distinguish BD from HC (38 genera, AUC = 0.961), SCH from HC (32 genera, AUC = 0.962), and BD from Scheme (13 genera, AUC = 0.823). Potential diagnostic biomarkers that can distinguish BD‐D from SCH‐N (16 genera, AUC = 0.969) and BD‐M from SCH‐P (31 genera, AUC = 0.938) were also identified. CONCLUSION: This study provides further understanding of abnormal gut microbiome in emerging adulthood patients with SCH and BD and lay the potential foundation for the development of microbe‐based clinical diagnosis for BD and SCH. John Wiley and Sons Inc. 2022-12-05 /pmc/articles/PMC10314106/ /pubmed/36468448 http://dx.doi.org/10.1111/cns.14044 Text en © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Chen, Yi‐huan
Zhou, Cui‐hong
Yu, Huan
Wu, Wen‐jun
Wang, Ying‐wei
Liu, Ling
Hu, Guang‐tao
Li, Bao‐juan
Peng, Zheng‐wu
Wang, Hua‐ning
Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood
title Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood
title_full Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood
title_fullStr Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood
title_full_unstemmed Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood
title_short Gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood
title_sort gut microbial signatures and differences in bipolar disorder and schizophrenia of emerging adulthood
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314106/
https://www.ncbi.nlm.nih.gov/pubmed/36468448
http://dx.doi.org/10.1111/cns.14044
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