4.6 Article

Gut Microbiota-Derived Inflammation-Related Serum Metabolites as Potential Biomarkers for Major Depressive Disorder

期刊

JOURNAL OF INFLAMMATION RESEARCH
卷 14, 期 -, 页码 3755-3766

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/JIR.S324922

关键词

major depressive disorder; gut microbiota; biomarkers; inflammation; metabolite

资金

  1. Natural Science Foundation Project of China [81701360, 81901398]
  2. Science and Technology Fund of Guizhou Province [(QianHe LH2015) 7411]
  3. Open Project Funding of Shanghai Key Laboratory of Forensic Medicine (Academy of Forensic Science)
  4. Natural Science Foundation of Chongqing, China [cstc2019jcyjmsxmX0025]
  5. Chongqing Yuzhong District Science & Technology Commission [20190115]

向作者/读者索取更多资源

By analyzing serum metabolomics and fecal microbial communities, this study identified potential biomarkers for MDD related to inflammation, which showed significant correlations with genera belonged to phyla Firmicutes and were able to effectively distinguish MDD patients from healthy controls.
Background: Although many works have been conducted to explore the biomarkers for diagnosing major depressive disorder (MDD), the widely accepted biomarkers are still not identified. Thus, the combined application of serum metabolomics and fecal microbial communities was used to identify gut microbiota-derived inflammation-related serum metabolites as potential biomarkers for MDD. Methods: MDD patients and healthy controls (HCs) were included in this study. Both serum samples and fecal samples were collected. The liquid chromatography mass spectrometry (LC-MS) was used to detect the metabolites in serum samples, and the 16S rRNA gene sequencing was used to analyze the gut microbiota compositions in fecal samples. Results: Totally, 60 MDD patients and 60 HCs were recruited. The 24 differential serum metabolites were identified, and 10 of these were inflammation-related metabolites. Three significantly affected inflammation-related pathways were identified using differential metabolites. The 17 differential genera were identified, and 14 of these genera belonged to phyla Firmicutes. Four significantly affected inflammation-related pathways were identified using differential genera. Five inflammation-related metabolites (LysoPC(16:0), deoxycholic acid, docosahexaenoic acid, taurocholic acid and LysoPC(20:0)) were identified as potential biomarkers. These potential biomarkers had significant correlations with genera belonged to phyla Firmicutes. The panel consisting of these biomarkers could effectively distinguish MDD patients from HCs with an area under the curve (AUC) of 0.95 in training set and 0.92 in testing set. Conclusion: These findings suggested that the disturbance of phyla Firmicutes might be involved in the onset of depression by regulating host's inflammatory response, and these potential biomarkers could be useful for future investigating the objective methods for diagnosing MDD.

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