Plasma Metabolomics Profiling of Metabolic Pathways Affected by Major Depressive Disorder

被引:17
|
作者
Du, Yue [1 ,2 ]
Wei, Jinxue [1 ,2 ,3 ]
Zhang, Zijian [1 ,2 ]
Yang, Xiao [1 ,2 ]
Wang, Min [1 ,2 ]
Wang, Yu [1 ,2 ]
Qi, Xiongwei [1 ,2 ]
Zhao, Liansheng [1 ,2 ,3 ]
Tian, Yang [1 ,2 ]
Guo, Wanjun [1 ,2 ,3 ]
Wang, Qiang [1 ,2 ,3 ]
Deng, Wei [1 ,2 ,3 ]
Li, Minli [1 ,2 ,3 ]
Lin, Dongtao [4 ]
Li, Tao [1 ,2 ,3 ]
Ma, Xiaohong [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, Psychiat Lab, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Mental Hlth Ctr, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, West China Brain Res Ctr, Chengdu, Peoples R China
[4] Sichuan Univ, Coll Foreign Languages & Cultures, Chengdu, Peoples R China
来源
FRONTIERS IN PSYCHIATRY | 2021年 / 12卷
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
major depressive disorder; metabolomics; metabolic pathway; glycine and serine metabolism; anxiety; EXCITATORY AMINO-ACIDS; TYROSINE METABOLISM; ANXIETY; SERINE; MECHANISMS; BIOMARKERS; PATTERNS; TAURINE; GLYCINE; MICE;
D O I
10.3389/fpsyt.2021.644555
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Major depressive disorder (MDD) is a common disease which is complicated by metabolic disorder. Although MDD has been studied relatively intensively, its metabolism is yet to be elucidated. Methods: To profile the global pathophysiological processes of MDD patients, we used metabolomics to identify differential metabolites and applied a new database Metabolite set enrichment analysis (MSEA) to discover dysfunctions of metabolic pathways of this disease. Hydrophilic metabolomics were applied to identify metabolites by profiling the plasma from 55 MDD patients and 100 sex-, gender-, BMI-matched healthy controls. The metabolites were then analyzed in MSEA in an attempt to discover different metabolic pathways. To investigate dysregulated pathways, we further divided MDD patients into two cohorts: (1) MDD patients with anxiety symptoms and (2) MDD patients without anxiety symptoms. Results: Metabolites which were hit in those pathways correlated with depressive and anxiety symptoms. Altogether, 17 metabolic pathways were enriched in MDD patients, and 23 metabolites were hit in those pathways. Three metabolic pathways were enriched in MDD patients without anxiety, including glycine and serine metabolism, arginine and proline metabolism, and phenylalanine and tyrosine metabolism. In addition, L-glutamic acid was positively correlated with the severity of depression and retardation if hit in MDD patients without anxiety symptoms. Conclusions: Different kinds of metabolic pathophysiological processes were found in MDD patients. Disorder of glycine and serine metabolism was observed in both MDD patients with anxiety and those without.
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页数:9
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