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Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder

BACKGROUND: Gut microbiota can affect human behavior and mood in many ways. Several studies have shown that patients with depression were also accompanied with gut microbiota disorder, in which Firmicutes are related to the protective function of intestinal barrier. In this study, we explore the cha...

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Autores principales: Huang, Yichen, Shi, Xing, Li, Zhiyong, Shen, Yang, Shi, Xinxin, Wang, Liying, Li, Gaofei, Yuan, Ye, Wang, Jixiang, Zhang, Yongchao, Zhao, Lei, Zhang, Meng, Kang, Yu, Liang, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284853/
https://www.ncbi.nlm.nih.gov/pubmed/30584306
http://dx.doi.org/10.2147/NDT.S188340
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author Huang, Yichen
Shi, Xing
Li, Zhiyong
Shen, Yang
Shi, Xinxin
Wang, Liying
Li, Gaofei
Yuan, Ye
Wang, Jixiang
Zhang, Yongchao
Zhao, Lei
Zhang, Meng
Kang, Yu
Liang, Ying
author_facet Huang, Yichen
Shi, Xing
Li, Zhiyong
Shen, Yang
Shi, Xinxin
Wang, Liying
Li, Gaofei
Yuan, Ye
Wang, Jixiang
Zhang, Yongchao
Zhao, Lei
Zhang, Meng
Kang, Yu
Liang, Ying
author_sort Huang, Yichen
collection PubMed
description BACKGROUND: Gut microbiota can affect human behavior and mood in many ways. Several studies have shown that patients with depression were also accompanied with gut microbiota disorder, in which Firmicutes are related to the protective function of intestinal barrier. In this study, we explore the changes and effects of Firmicutes in the patients with major depressive disorder (MDD). METHOD: We recruited 54 subjects, including 27 patients with MDD. Fecal samples were collected for identification by 16S rRNA sequencing and bioinformatics analysis. RESULTS: The study shows that the alpha diversity indices of MDD patients are lower than those of the healthy controls. Firmicutes is the most significantly decreased phylum in the MDD samples. There are totally 13 taxonomic biomarkers with P-value <0.01 from Firmicutes. There are differences in 17 KEGG pathways between the two groups. CONCLUSION: This study found that there is a significant disorder of gut microbiota in the patients with depression, in which the Firmicutes decreased significantly. Defects of the Firmicutes may lead to the depression in short-chain fatty acids, which could account for the physiological basis of low-level inflammation of depression. LIMITATIONS: This is a cross-sectional study and the sample size is comparatively small. Though several diet-related factors were controlled in the study, there is no quantified assessment of it.
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spelling pubmed-62848532018-12-24 Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder Huang, Yichen Shi, Xing Li, Zhiyong Shen, Yang Shi, Xinxin Wang, Liying Li, Gaofei Yuan, Ye Wang, Jixiang Zhang, Yongchao Zhao, Lei Zhang, Meng Kang, Yu Liang, Ying Neuropsychiatr Dis Treat Clinical Trial Report BACKGROUND: Gut microbiota can affect human behavior and mood in many ways. Several studies have shown that patients with depression were also accompanied with gut microbiota disorder, in which Firmicutes are related to the protective function of intestinal barrier. In this study, we explore the changes and effects of Firmicutes in the patients with major depressive disorder (MDD). METHOD: We recruited 54 subjects, including 27 patients with MDD. Fecal samples were collected for identification by 16S rRNA sequencing and bioinformatics analysis. RESULTS: The study shows that the alpha diversity indices of MDD patients are lower than those of the healthy controls. Firmicutes is the most significantly decreased phylum in the MDD samples. There are totally 13 taxonomic biomarkers with P-value <0.01 from Firmicutes. There are differences in 17 KEGG pathways between the two groups. CONCLUSION: This study found that there is a significant disorder of gut microbiota in the patients with depression, in which the Firmicutes decreased significantly. Defects of the Firmicutes may lead to the depression in short-chain fatty acids, which could account for the physiological basis of low-level inflammation of depression. LIMITATIONS: This is a cross-sectional study and the sample size is comparatively small. Though several diet-related factors were controlled in the study, there is no quantified assessment of it. Dove Medical Press 2018-12-03 /pmc/articles/PMC6284853/ /pubmed/30584306 http://dx.doi.org/10.2147/NDT.S188340 Text en © 2018 Huang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Clinical Trial Report
Huang, Yichen
Shi, Xing
Li, Zhiyong
Shen, Yang
Shi, Xinxin
Wang, Liying
Li, Gaofei
Yuan, Ye
Wang, Jixiang
Zhang, Yongchao
Zhao, Lei
Zhang, Meng
Kang, Yu
Liang, Ying
Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder
title Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder
title_full Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder
title_fullStr Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder
title_full_unstemmed Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder
title_short Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder
title_sort possible association of firmicutes in the gut microbiota of patients with major depressive disorder
topic Clinical Trial Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284853/
https://www.ncbi.nlm.nih.gov/pubmed/30584306
http://dx.doi.org/10.2147/NDT.S188340
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