Gut microbiota and inflammatory factor characteristics in major depressive disorder patients with anorexia.


Journal

BMC psychiatry
ISSN: 1471-244X
Titre abrégé: BMC Psychiatry
Pays: England
ID NLM: 100968559

Informations de publication

Date de publication:
02 May 2024
Historique:
received: 30 10 2023
accepted: 18 04 2024
medline: 3 5 2024
pubmed: 3 5 2024
entrez: 2 5 2024
Statut: epublish

Résumé

This study aimed to explore the gut microbiota and inflammatory factor characteristics in major depressive disorder (MDD) patients with anorexia and to analyze the correlation between gut microbiota and inflammatory factors, anorexia, and HAMD scores. 46 MDD patients and 46 healthy controls (HC) were included in the study. The 46 MDD patients were divided into two groups according to whether they had anorexia:20 MDD without anorexia (MDA0 group) and 26 MDD with anorexia (MDA1 group). We used the Hamilton Depression Scale-24 (HAMD-24) to evaluate the depression status of all participants and 16 S ribosomal RNA (16 S rRNA)sequencing to evaluate the composition of the gut microbiota. Inflammatory factors in peripheral blood such as C-reactive protein (CRP) were detected using enzyme-linked immunosorbent assay (ELISA). Spearman's correlation analysis was used to evaluate the correlation between gut microbiota and inflammatory factors, HAMD scores, and anorexia. 1). CRP was significantly higher in the MDA0, MDA1, than HC. 2). An analysis of α-diversity shows: the Simpson and Pielou indices of the HC group are higher than the MDA1 group (P < 0.05). 3). The β-diversity analysis shows differences in the composition of microbial communities between the MDA0, MDA1, and HC group. 4). A correlation analysis showed that Blautia positively correlated with anorexia, HAMD scores, and CRP level, whereas Faecalibacterium, Bacteroides, Roseburia, and Parabacteroides negatively correlated with anorexia, HAMD scores, and CRP level. 5). The receiver operating characteristic (ROC) curve was drawn using the differential bacterial genera between MDD patients with or without anorexia as biomarkers to identify whether MDD patients were accompanied with anorexia, and its area under curve (AUC) was 0.85. The ROC curve was drawn using the differential bacterial genera between MDD patients with anorexia and healthy controls as biomarkers to diagnose MDD patients with anorexia, with its AUC was 0.97. This study suggested that MDD patients with anorexia had a distinct gut microbiota compared to healthy individuals, with higher level of CRP. Blautia was more abundant in MDD patients with anorexia and positively correlated with CRP, HAMD scores, and anorexia. The gut microbiota might have influenced MDD and anorexia through the inflammatory factor CRP.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed to explore the gut microbiota and inflammatory factor characteristics in major depressive disorder (MDD) patients with anorexia and to analyze the correlation between gut microbiota and inflammatory factors, anorexia, and HAMD scores.
METHODS METHODS
46 MDD patients and 46 healthy controls (HC) were included in the study. The 46 MDD patients were divided into two groups according to whether they had anorexia:20 MDD without anorexia (MDA0 group) and 26 MDD with anorexia (MDA1 group). We used the Hamilton Depression Scale-24 (HAMD-24) to evaluate the depression status of all participants and 16 S ribosomal RNA (16 S rRNA)sequencing to evaluate the composition of the gut microbiota. Inflammatory factors in peripheral blood such as C-reactive protein (CRP) were detected using enzyme-linked immunosorbent assay (ELISA). Spearman's correlation analysis was used to evaluate the correlation between gut microbiota and inflammatory factors, HAMD scores, and anorexia.
RESULTS RESULTS
1). CRP was significantly higher in the MDA0, MDA1, than HC. 2). An analysis of α-diversity shows: the Simpson and Pielou indices of the HC group are higher than the MDA1 group (P < 0.05). 3). The β-diversity analysis shows differences in the composition of microbial communities between the MDA0, MDA1, and HC group. 4). A correlation analysis showed that Blautia positively correlated with anorexia, HAMD scores, and CRP level, whereas Faecalibacterium, Bacteroides, Roseburia, and Parabacteroides negatively correlated with anorexia, HAMD scores, and CRP level. 5). The receiver operating characteristic (ROC) curve was drawn using the differential bacterial genera between MDD patients with or without anorexia as biomarkers to identify whether MDD patients were accompanied with anorexia, and its area under curve (AUC) was 0.85. The ROC curve was drawn using the differential bacterial genera between MDD patients with anorexia and healthy controls as biomarkers to diagnose MDD patients with anorexia, with its AUC was 0.97.
CONCLUSION CONCLUSIONS
This study suggested that MDD patients with anorexia had a distinct gut microbiota compared to healthy individuals, with higher level of CRP. Blautia was more abundant in MDD patients with anorexia and positively correlated with CRP, HAMD scores, and anorexia. The gut microbiota might have influenced MDD and anorexia through the inflammatory factor CRP.

Identifiants

pubmed: 38698338
doi: 10.1186/s12888-024-05778-0
pii: 10.1186/s12888-024-05778-0
doi:

Substances chimiques

C-Reactive Protein 9007-41-4
RNA, Ribosomal, 16S 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

334

Subventions

Organisme : National Natural Science Foundation of China
ID : 82201691
Organisme : Shanxi Provincial Science and Technology Department
ID : 20210302124193

Informations de copyright

© 2024. The Author(s).

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Auteurs

Fengtao Guo (F)

Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Shanxi Medical University, Taiyuan, 030001, China.
Yanhu District Branch, The First Hospital of Shanxi Medical University, Yuncheng, 044000, China.

Lin Jing (L)

Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Shanxi Medical University, Taiyuan, 030001, China.

Yunfan Xu (Y)

Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Shanxi Medical University, Taiyuan, 030001, China.

Kun Zhang (K)

Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Shanxi Medical University, Taiyuan, 030001, China.

Ying Li (Y)

Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Shanxi Medical University, Taiyuan, 030001, China.

Ning Sun (N)

Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.

Penghong Liu (P)

Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, 030001, China. liupenghong6@163.com.
Shanxi Medical University, Taiyuan, 030001, China. liupenghong6@163.com.

Huanhu Zhang (H)

Shanxi Medical University, Taiyuan, 030001, China. zhhh31@163.com.
Shanxi University of Chinese Medicine, Jinzhong, 030619, China. zhhh31@163.com.

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