Polyunsaturated fatty acids metabolism, purine metabolism and inosine as potential independent diagnostic biomarkers for major depressive disorder in children and adolescents

被引:0
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作者
Xinyu Zhou
Lanxiang Liu
Xinghui Lan
David Cohen
Yuqing Zhang
Arun V Ravindran
Shuai Yuan
Peng Zheng
David Coghill
Lining Yang
Sarah E Hetrick
Xiaofeng Jiang
Jean-Jacques Benoliel
Andrea Cipriani
Peng Xie
机构
[1] The First Affiliated Hospital of Chongqing Medical University,Department of Psychiatry
[2] Chongqing Medical University,Institute of Neuroscience and the Collaborative Innovation Center for Brain Science
[3] Children’s Hospital of Chongqing Medical University,Department of Psychiatry
[4] Université Pierre et Marie Curie,Department of Child and Adolescent Psychiatry, Hôpital Pitié–Salpétrière, Institut des Systèmes Intelligents et Robotiques
[5] University of Toronto,Department of Psychiatry
[6] University of Melbourne,Departments of Paediatrics and Psychiatry
[7] University of Melbourne,Centre for Youth Mental Health
[8] University of Auckland,Department of Psychological Medicine
[9] Universite´ Pierre et Marie Curie-Paris 6,UMRS 975, Pain Team, Site Pitie´
[10] Warneford Hospital,Salpeˆtrie’re
[11] Oxford Health NHS Foundation Trust,Department of Psychiatry, University of Oxford
来源
Molecular Psychiatry | 2019年 / 24卷
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摘要
Major depressive disorder (MDD) in children and adolescents is a recurrent and disabling condition globally but its pathophysiology remains poorly elucidated and there are limited effective treatments available. We performed metabolic profiling of plasma samples based on ultra-high-performance liquid chromatography equipped with quadrupole time-offlight mass spectrometry to explore the potential biomarkers of depression in children and adolescents with MDD. We identified several perturbed pathways, including fatty acid metabolism—particularly the polyunsaturated fatty acids metabolism, and purine metabolism—that were associated with MDD in these young patients. In addition, inosine was shown as a potential independent diagnostic biomarker for MDD, achieving an area under the ROC curve of 0.999 in discriminating drug-naive MDD patients and 0.866 in discriminating drug-treated MDD from healthy controls. Moreover, we found evidence for differences in the pathophysiology of MDD in children and adolescents to that of adult MDD, specifically with tryptophan metabolism. Through metabolomic analysis, we have identified links between a framework of metabolic perturbations and the pathophysiology and diagnostic biomarker of child and adolescent MDD.
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页码:1478 / 1488
页数:10
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