The gut microbiome in social anxiety disorder: evidence of altered composition and function

被引:49
作者
Butler, Mary I. I. [1 ,2 ]
Bastiaanssen, Thomaz F. S. [2 ,3 ]
Long-Smith, Caitriona [2 ]
Morkl, Sabrina [1 ,4 ]
Berding, Kirsten [2 ]
Ritz, Nathaniel L. L. [2 ]
Strain, Conall [2 ,5 ]
Patangia, Dhrati [2 ,5 ]
Patel, Shriram [2 ,6 ]
Stanton, Catherine [2 ,6 ]
O'Mahony, Siobhain M. M. [2 ,3 ]
Cryan, John F. F. [2 ,3 ]
Clarke, Gerard [1 ,2 ]
Dinan, Timothy G. G. [1 ,2 ]
机构
[1] Univ Coll Cork, Dept Psychiat & Neurobehav Sci, Cork, Ireland
[2] Univ Coll Cork, APC Microbiome Ireland, Cork, Ireland
[3] Univ Coll Cork, Dept Anat & Neurosci, Cork, Ireland
[4] Med Univ Graz, Dept Psychiat & Psychotherapeut Med, Graz, Austria
[5] Teagasc Food Res Programme, Moorepk, Fermoy T12 YN60, Cork, Ireland
[6] Univ Coll Cork, Sch Microbiol, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
RANDOMIZED CONTROLLED-TRIAL; ASPARTATE-AMINOTRANSFERASE; KYNURENIC ACID; D-CYCLOSERINE; SELF-REPORT; PSYCHOMETRIC PROPERTIES; ESCHERICHIA-COLI; EXPOSURE THERAPY; FECAL MICROBIOTA; STRESS-RESPONSE;
D O I
10.1038/s41398-023-02325-5
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The microbiome-gut-brain axis plays a role in anxiety, the stress response and social development, and is of growing interest in neuropsychiatric conditions. The gut microbiota shows compositional alterations in a variety of psychiatric disorders including depression, generalised anxiety disorder (GAD), autism spectrum disorder (ASD) and schizophrenia but studies investigating the gut microbiome in social anxiety disorder (SAD) are very limited. Using whole-genome shotgun analysis of 49 faecal samples (31 cases and 18 sex- and age-matched controls), we analysed compositional and functional differences in the gut microbiome of patients with SAD in comparison to healthy controls. Overall microbiota composition, as measured by beta-diversity, was found to be different between the SAD and control groups and several taxonomic differences were seen at a genus- and species-level. The relative abundance of the genera Anaeromassillibacillus and Gordonibacter were elevated in SAD, while Parasuterella was enriched in healthy controls. At a species-level, Anaeromassilibacillus sp An250 was found to be more abundant in SAD patients while Parasutterella excrementihominis was higher in controls. No differences were seen in alpha diversity. In relation to functional differences, the gut metabolic module 'aspartate degradation I' was elevated in SAD patients. In conclusion, the gut microbiome of patients with SAD differs in composition and function to that of healthy controls. Larger, longitudinal studies are warranted to validate these preliminary results and explore the clinical implications of these microbiome changes.
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页数:12
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