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Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study

BACKGROUND: To explore the gut microbiota characteristics in depressed patients with bipolar disorder (BD) as well as the connection between the gut microbiota and inflammatory markers. METHODS: Totally 72 depressed BD patients and 16 healthy controls (HCs) were enrolled in the study. Blood and fece...

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Autores principales: Huang, Tingting, Shang, Yushan, Dai, Chunxiao, Zhang, Qixiu, Hu, Shaohua, Xie, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197851/
https://www.ncbi.nlm.nih.gov/pubmed/37208752
http://dx.doi.org/10.1186/s12991-023-00453-2
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author Huang, Tingting
Shang, Yushan
Dai, Chunxiao
Zhang, Qixiu
Hu, Shaohua
Xie, Jian
author_facet Huang, Tingting
Shang, Yushan
Dai, Chunxiao
Zhang, Qixiu
Hu, Shaohua
Xie, Jian
author_sort Huang, Tingting
collection PubMed
description BACKGROUND: To explore the gut microbiota characteristics in depressed patients with bipolar disorder (BD) as well as the connection between the gut microbiota and inflammatory markers. METHODS: Totally 72 depressed BD patients and 16 healthy controls (HCs) were enrolled in the study. Blood and feces samples were taken from each subject. With the help of 16S-ribosomal RNA gene sequencing, the characteristics of the gut microbiota in each participant were examined. Correlation analysis was then utilized to assess the relationship between the gut microbiota and clinical parameters. RESULTS: We found the taxonomic composition of the gut microbiota, but not its diversity, was significantly different in BD patients compared to HCs. We found the abundance of Bacilli, Lactobacillales and genus Veillonella were higher in BD patients than in HCs, while genus Dorea was more abundant in HCs. Additionally, correlation analysis showed that the bacterial genera’ abundance in BD patients was strongly correlated with the severity of depression and inflammatory markers. CONCLUSIONS: According to these results, the gut microbiota characteristics were changed in depressed BD patients, which may have been associated with the severity of depression and the inflammatory pathways.
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spelling pubmed-101978512023-05-20 Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study Huang, Tingting Shang, Yushan Dai, Chunxiao Zhang, Qixiu Hu, Shaohua Xie, Jian Ann Gen Psychiatry Research BACKGROUND: To explore the gut microbiota characteristics in depressed patients with bipolar disorder (BD) as well as the connection between the gut microbiota and inflammatory markers. METHODS: Totally 72 depressed BD patients and 16 healthy controls (HCs) were enrolled in the study. Blood and feces samples were taken from each subject. With the help of 16S-ribosomal RNA gene sequencing, the characteristics of the gut microbiota in each participant were examined. Correlation analysis was then utilized to assess the relationship between the gut microbiota and clinical parameters. RESULTS: We found the taxonomic composition of the gut microbiota, but not its diversity, was significantly different in BD patients compared to HCs. We found the abundance of Bacilli, Lactobacillales and genus Veillonella were higher in BD patients than in HCs, while genus Dorea was more abundant in HCs. Additionally, correlation analysis showed that the bacterial genera’ abundance in BD patients was strongly correlated with the severity of depression and inflammatory markers. CONCLUSIONS: According to these results, the gut microbiota characteristics were changed in depressed BD patients, which may have been associated with the severity of depression and the inflammatory pathways. BioMed Central 2023-05-19 /pmc/articles/PMC10197851/ /pubmed/37208752 http://dx.doi.org/10.1186/s12991-023-00453-2 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Huang, Tingting
Shang, Yushan
Dai, Chunxiao
Zhang, Qixiu
Hu, Shaohua
Xie, Jian
Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study
title Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study
title_full Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study
title_fullStr Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study
title_full_unstemmed Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study
title_short Gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study
title_sort gut microbiota and its relation to inflammation in patients with bipolar depression: a cross-sectional study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197851/
https://www.ncbi.nlm.nih.gov/pubmed/37208752
http://dx.doi.org/10.1186/s12991-023-00453-2
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