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Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias

INTRODUCTION: Evidence suggests that negative cognitive processing bias (NCPB) is a significant risk factor for depression. The microbiota–gut–brain axis has been proven to be a contributing factor to cognitive health and disease. However, the connection between microbiota and NCPB remains unknown....

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Autores principales: Xu, Hui-Min, Xie, Shen-Wei, Liu, Tian-Yao, Zhou, Xia, Feng, Zheng-Zhi, He, Xie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015002/
https://www.ncbi.nlm.nih.gov/pubmed/36937259
http://dx.doi.org/10.3389/fmicb.2023.989162
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author Xu, Hui-Min
Xie, Shen-Wei
Liu, Tian-Yao
Zhou, Xia
Feng, Zheng-Zhi
He, Xie
author_facet Xu, Hui-Min
Xie, Shen-Wei
Liu, Tian-Yao
Zhou, Xia
Feng, Zheng-Zhi
He, Xie
author_sort Xu, Hui-Min
collection PubMed
description INTRODUCTION: Evidence suggests that negative cognitive processing bias (NCPB) is a significant risk factor for depression. The microbiota–gut–brain axis has been proven to be a contributing factor to cognitive health and disease. However, the connection between microbiota and NCPB remains unknown. This study mainly sought to explore the key microbiota involved in NCPB and the possible pathways through which NCPB affects depressive symptoms. METHODS: Data in our studies were collected from 735 Chinese young adults through a cross-sectional survey. Fecal samples were collected from 35 young adults with different levels of NCPB (18 individuals were recruited as the high-status NCPB group, and another 17 individuals were matched as the low-status NCPB group) and 60 with different degrees of depressive symptoms (27 individuals were recruited into the depressive symptom group, as D group, and 33 individuals were matched into the control group, as C group) and analyzed by the 16S ribosomal RNA sequencing technique. RESULTS: As a result, the level of NCPB correlated with the degree of depressive symptoms as well as anxiety symptoms and sleep quality (p < 0.01). The β-diversity of microbiota in young adults was proven to be significantly different between the high-status NCPB and the low-status NCPB groups. There were several significantly increased bacteria taxa, including Dorea, Christensenellaceae, Christe -senellaceae_R_7_group, Ruminococcaceae_NK4A214_group, Eggerthellaceae, Family-XIII, Family_XIII_AD3011_group, Faecalibaculum, and Oscillibacter. They were mainly involved in pathways including short-chain fatty acid (SCFA) metabolism. Among these variable bacteria taxa, Faecalibaculum was found associated with both NCPB and depressive symptoms. Furthermore, five pathways turned out to be significantly altered in both the high-status NCPB group and the depressive symptom group, including butanoate metabolism, glyoxylate and dicarboxylate metabolism, propanoate metabolism, phenylalanine, tyrosine, and tryptophan biosynthesis, valine, leucine, and isoleucine degradation. These pathways were related to SCFA metabolism. DISCUSSION: Fecal microbiota is altered in Chinese young male adults with high status NCPB and may be involved in the biochemical progress that influences depressive symptoms.
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spelling pubmed-100150022023-03-16 Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias Xu, Hui-Min Xie, Shen-Wei Liu, Tian-Yao Zhou, Xia Feng, Zheng-Zhi He, Xie Front Microbiol Microbiology INTRODUCTION: Evidence suggests that negative cognitive processing bias (NCPB) is a significant risk factor for depression. The microbiota–gut–brain axis has been proven to be a contributing factor to cognitive health and disease. However, the connection between microbiota and NCPB remains unknown. This study mainly sought to explore the key microbiota involved in NCPB and the possible pathways through which NCPB affects depressive symptoms. METHODS: Data in our studies were collected from 735 Chinese young adults through a cross-sectional survey. Fecal samples were collected from 35 young adults with different levels of NCPB (18 individuals were recruited as the high-status NCPB group, and another 17 individuals were matched as the low-status NCPB group) and 60 with different degrees of depressive symptoms (27 individuals were recruited into the depressive symptom group, as D group, and 33 individuals were matched into the control group, as C group) and analyzed by the 16S ribosomal RNA sequencing technique. RESULTS: As a result, the level of NCPB correlated with the degree of depressive symptoms as well as anxiety symptoms and sleep quality (p < 0.01). The β-diversity of microbiota in young adults was proven to be significantly different between the high-status NCPB and the low-status NCPB groups. There were several significantly increased bacteria taxa, including Dorea, Christensenellaceae, Christe -senellaceae_R_7_group, Ruminococcaceae_NK4A214_group, Eggerthellaceae, Family-XIII, Family_XIII_AD3011_group, Faecalibaculum, and Oscillibacter. They were mainly involved in pathways including short-chain fatty acid (SCFA) metabolism. Among these variable bacteria taxa, Faecalibaculum was found associated with both NCPB and depressive symptoms. Furthermore, five pathways turned out to be significantly altered in both the high-status NCPB group and the depressive symptom group, including butanoate metabolism, glyoxylate and dicarboxylate metabolism, propanoate metabolism, phenylalanine, tyrosine, and tryptophan biosynthesis, valine, leucine, and isoleucine degradation. These pathways were related to SCFA metabolism. DISCUSSION: Fecal microbiota is altered in Chinese young male adults with high status NCPB and may be involved in the biochemical progress that influences depressive symptoms. Frontiers Media S.A. 2023-03-01 /pmc/articles/PMC10015002/ /pubmed/36937259 http://dx.doi.org/10.3389/fmicb.2023.989162 Text en Copyright © 2023 Xu, Xie, Liu, Zhou, Feng and He. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Xu, Hui-Min
Xie, Shen-Wei
Liu, Tian-Yao
Zhou, Xia
Feng, Zheng-Zhi
He, Xie
Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias
title Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias
title_full Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias
title_fullStr Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias
title_full_unstemmed Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias
title_short Microbiota alteration of Chinese young male adults with high-status negative cognitive processing bias
title_sort microbiota alteration of chinese young male adults with high-status negative cognitive processing bias
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015002/
https://www.ncbi.nlm.nih.gov/pubmed/36937259
http://dx.doi.org/10.3389/fmicb.2023.989162
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