4.7 Article

Altered fecal microbiota composition in patients with major depressive disorder

期刊

BRAIN BEHAVIOR AND IMMUNITY
卷 48, 期 -, 页码 186-194

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2015.03.016

关键词

Depression; Gut bacteria; Inflammation; Gut-brain; Antidepressant

资金

  1. National Key Stone Basic Research Program (973 Program) of China [2013CB531401]
  2. Major Projects of Science Research for the 12th Five-Year Plan of China [2013ZX10004904, 2011ZX10004901]
  3. Fundamental Research Funds for the Central Universities, China [2014XZZX008, 2013XZZX008]

向作者/读者索取更多资源

Studies using animal models have shown that depression affects the stability of the microbiota, but the actual structure and composition in patients with major depressive disorder (MDD) are not well understood. Here, we analyzed fecal samples from 46 patients with depression (29 active-MDD and 17 responded-MDD) and 30 healthy controls (HCs). High-throughput pyrosequencing showed that, according to the Shannon index, increased fecal bacterial alpha-diversity was found in the active-MDD (A-MDD) vs. the HC group but not in the responded-MDD (R-MDD) vs. the HC group. Bacteroidetes, Proteobacteria, and Actinobacteria strongly increased in level, whereas that of Firmicutes was significantly reduced in the A-MDD and R-MDD groups compared with the HC group. Despite profound interindividual variability, levels of several predominant genera were significantly different between the MDD and HC groups. Most notably, the MDD groups had increased levels of Enterobacteriaceae and Alistipes but reduced levels of Faecalibacterium. A negative correlation was observed between Faecalibacterium and the severity of depressive symptoms. These findings enable a better understanding of changes in the fecal microbiota composition in such patients, showing either a predominance of some potentially harmful bacterial groups or a reduction in beneficial bacterial genera. Further studies are warranted to elucidate the temporal and causal relationships between gut microbiota and depression and to evaluate the suitability of the microbiome as a biomarker. (C) 2015 The Authors. Published by Elsevier Inc.

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