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多不饱和脂肪酸代谢、嘌呤代谢和肌苷作为儿童和青少年重度抑郁症潜在的独立诊断生物标志物。

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

机构信息

Department of Psychiatry, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Institute of Neuroscience and the Collaborative Innovation Center for Brain Science, Chongqing Medical University, Chongqing, China.

出版信息

Mol Psychiatry. 2019 Oct;24(10):1478-1488. doi: 10.1038/s41380-018-0047-z. Epub 2018 Apr 20.

Abstract

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.

摘要

儿童和青少年重度抑郁症(MDD)是一种在全球范围内反复发作且致残的疾病,但它的病理生理学仍未得到充分阐明,并且有效的治疗方法有限。我们对基于超高效液相色谱-四极杆飞行时间质谱的血浆样本进行了代谢组学分析,以探索儿童和青少年 MDD 潜在的生物标志物。我们发现了几个失调的途径,包括脂肪酸代谢-特别是多不饱和脂肪酸代谢和嘌呤代谢-与这些年轻患者的 MDD 相关。此外,肌苷被证明是 MDD 的一个潜在的独立诊断生物标志物,在区分未经药物治疗的 MDD 患者和区分药物治疗的 MDD 患者与健康对照方面,ROC 曲线下面积分别达到 0.999 和 0.866。此外,我们发现儿童和青少年 MDD 的病理生理学与成人 MDD 的病理生理学存在差异,特别是色氨酸代谢。通过代谢组学分析,我们已经确定了代谢失调框架与儿童和青少年 MDD 的病理生理学和诊断生物标志物之间的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3a8/6756100/e7f63137c8f1/41380_2018_47_Fig1_HTML.jpg

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