Department of Neurology, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402460, China.
Chongqing Key Laboratory of Neurobiology, Chongqing, 400016, China.
Transl Psychiatry. 2018 Jul 10;8(1):130. doi: 10.1038/s41398-018-0183-x.
Major depressive disorder (MDD) is a debilitating psychiatric illness. However, there is currently no objective laboratory-based diagnostic tests for this disorder. Although, perturbations in multiple neurotransmitter systems have been implicated in MDD, the biochemical changes underlying the disorder remain unclear, and a comprehensive global evaluation of neurotransmitters in MDD has not yet been performed. Here, using a GC-MS coupled with LC-MS/MS-based targeted metabolomics approach, we simultaneously quantified the levels of 19 plasma metabolites involved in GABAergic, catecholaminergic, and serotonergic neurotransmitter systems in 50 first-episode, antidepressant drug-naïve MDD subjects and 50 healthy controls to identify potential metabolite biomarkers for MDD (training set). Moreover, an independent sample cohort comprising 49 MDD patients, 30 bipolar disorder (BD) patients and 40 healthy controls (testing set) was further used to validate diagnostic generalizability and specificity of these candidate biomarkers. Among the 19 plasma neurotransmitter metabolites examined, nine were significantly changed in MDD subjects. These metabolites were mainly involved in GABAergic, catecholaminergic and serotonergic systems. The GABAergic and catecholaminergic had better diagnostic value than serotonergic pathway. A panel of four candidate plasma metabolite biomarkers (GABA, dopamine, tyramine, kynurenine) could distinguish MDD subjects from health controls with an AUC of 0.968 and 0.953 in the training and testing set, respectively. Furthermore, this panel distinguished MDD subjects from BD subjects with high accuracy. This study is the first to globally evaluate multiple neurotransmitters in MDD plasma. The altered plasma neurotransmitter metabolite profile has potential differential diagnostic value for MDD.
重度抑郁症(MDD)是一种使人虚弱的精神疾病。然而,目前还没有基于实验室的客观诊断测试方法来诊断这种疾病。尽管多个神经递质系统的紊乱与 MDD 有关,但该疾病的生化变化仍不清楚,也尚未对 MDD 中的神经递质进行全面的全球评估。在这里,我们使用 GC-MS 结合基于 LC-MS/MS 的靶向代谢组学方法,同时定量测定了 50 名首次发作、未经抗抑郁药物治疗的 MDD 患者和 50 名健康对照者的 19 种与 GABA 能、儿茶酚胺和 5-羟色胺能神经递质系统相关的血浆代谢物的水平,以确定 MDD 的潜在代谢物生物标志物(训练集)。此外,我们还进一步使用包含 49 名 MDD 患者、30 名双相情感障碍(BD)患者和 40 名健康对照者的独立样本队列(测试集)来验证这些候选生物标志物的诊断通用性和特异性。在检查的 19 种血浆神经递质代谢物中,有 9 种在 MDD 患者中发生了显著变化。这些代谢物主要涉及 GABA 能、儿茶酚胺能和 5-羟色胺能系统。GABA 能和儿茶酚胺能的诊断价值优于 5-羟色胺能途径。一组四个候选血浆代谢物生物标志物(GABA、多巴胺、酪胺、犬尿氨酸)可以区分 MDD 患者和健康对照者,在训练集和测试集中的 AUC 分别为 0.968 和 0.953。此外,该模型可以准确地区分 MDD 患者和 BD 患者。这项研究首次全面评估了 MDD 血浆中的多种神经递质。改变的血浆神经递质代谢物谱对 MDD 具有潜在的差异诊断价值。