TY - JOUR
T1 - Polyunsaturated fatty acids metabolism, purine metabolism and inosine as potential independent diagnostic biomarkers for major depressive disorder in children and adolescents
AU - Zhou, Xinyu
AU - Liu, Lanxiang
AU - Lan, Xinghui
AU - Cohen, David
AU - Zhang, Yuqing
AU - Ravindran, Arun V.
AU - Yuan, Shuai
AU - Zheng, Peng
AU - Coghill, David
AU - Yang, Lining
AU - Hetrick, Sarah E.
AU - Jiang, Xiaofeng
AU - Benoliel, Jean Jacques
AU - Cipriani, Andrea
AU - Xie, Peng
N1 - Publisher Copyright:
© 2018, The Author(s).
PY - 2019/10/1
Y1 - 2019/10/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85045725541&partnerID=8YFLogxK
U2 - 10.1038/s41380-018-0047-z
DO - 10.1038/s41380-018-0047-z
M3 - Article
C2 - 29679072
AN - SCOPUS:85045725541
SN - 1359-4184
VL - 24
SP - 1478
EP - 1488
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 10
ER -