4.7 Article

Dysbiosis of the Gut Microbiota and Kynurenine (Kyn) Pathway Activity as Potential Biomarkers in Patients with Major Depressive Disorder

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NUTRIENTS
卷 15, 期 7, 页码 -

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MDPI
DOI: 10.3390/nu15071752

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major depressive disorder; gut microbiota; kynurenine; biomarkers

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Studies have shown that the gut microbiota is associated with neurological and psychiatric diseases. However, the changes in gut microbiota in patients with major depressive disorder (MDD) and their association with disease mechanisms are still unclear. This study recruited MDD patients and healthy controls, analyzed the compositional characteristics of the gut microbiota in MDD patients, and detected specific markers in their plasma. The results showed significant changes in the diversity and relative abundance of the gut microbiota in MDD patients, suggesting that these changes may potentially serve as biomarkers for MDD.
With increasing attention paid to the concept of the microbiota-gut-brain axis, mounting evidence reveals that the gut microbiota is involved in a variety of neurological and psychiatric diseases. However, gut microbiota changes in major depressive disorder (MDD) patients and their association with disease mechanisms remain undefined. Fifty MDD patients and sixty healthy controls were recruited from the Shanghai Healthy Mental Center, China. Fecal samples were collected, and the compositional characteristics of the intestinal flora were determined in MDD patients by MiSeq sequencing. Venous blood was collected for the detection of plasma indoleamine-2,3-dioxygenase (Ido), kynurenine (Kyn) and tryptophan (Trp) levels. Stool samples of bacterial 16S sequencing was carried out. A total of 2,705,809 optimized sequences were obtained, with an average of 54,116 per sample. More unique OTUs were observed at the family, genus and species levels in the control group compared with the MDD cases. Further analysis showed significant changes in the alpha- and beta-diversities and relative abundance levels of gut microbial entities in MDD patients, as well as elevated amounts of Ido and Kyn indicating Kyn pathway activation, KEGG bacterial 16S function prediction analysis shows a variety of amino acids and metabolic (including Ido, Trp and Kyn) changes in the body of patients with MDD. These may result in increased neurotoxic metabolites and reduced generation of serotonin in the disease process. These changed factors may potentially be utilized as biomarkers for MDD in the future, playing more important roles in the disease course.

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