Department of Psychiatry, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
Department of Neuropsychiatry, Seoul National University Hospital, Seoul 03080, Republic of Korea.
J Proteome Res. 2021 Jun 4;20(6):3188-3203. doi: 10.1021/acs.jproteome.1c00058. Epub 2021 May 7.
Because major depressive disorder (MDD) and bipolar disorder (BD) manifest with similar symptoms, misdiagnosis is a persistent issue, necessitating their differentiation through objective methods. This study was aimed to differentiate between these disorders using a targeted proteomic approach. Multiple reaction monitoring-mass spectrometry (MRM-MS) analysis was performed to quantify protein targets regarding the two disorders in plasma samples of 270 individuals (90 MDD, 90 BD, and 90 healthy controls (HCs)). In the training set (72 MDD and 72 BD), a generalizable model comprising nine proteins was developed. The model was evaluated in the test set (18 MDD and 18 BD). The model demonstrated a good performance (area under the curve (AUC) >0.8) in discriminating MDD from BD in the training (AUC = 0.84) and test sets (AUC = 0.81) and in distinguishing MDD from BD without current hypomanic/manic/mixed symptoms (90 MDD and 75 BD) (AUC = 0.83). Subsequently, the model demonstrated excellent performance for drug-free MDD versus BD (11 MDD and 10 BD) (AUC = 0.96) and good performance for MDD versus HC (AUC = 0.87) and BD versus HC (AUC = 0.86). Furthermore, the nine proteins were associated with neuro, oxidative/nitrosative stress, and immunity/inflammation-related biological functions. This proof-of-concept study introduces a potential model for distinguishing between the two disorders.
由于重度抑郁症(MDD)和双相情感障碍(BD)的表现症状相似,因此误诊是一个持续存在的问题,需要通过客观方法来区分这两种疾病。本研究旨在采用靶向蛋白质组学方法来区分这两种疾病。使用多反应监测-质谱(MRM-MS)分析对 270 名个体(90 名 MDD、90 名 BD 和 90 名健康对照(HC))的血浆样本中的蛋白质靶标进行定量。在训练集中(72 名 MDD 和 72 名 BD),开发了一种包含九个蛋白质的可推广模型。在测试集中(18 名 MDD 和 18 名 BD)对该模型进行了评估。该模型在训练集(AUC = 0.84)和测试集(AUC = 0.81)中均能很好地区分 MDD 和 BD,且在区分无当前轻躁狂/躁狂/混合症状的 MDD 和 BD(90 名 MDD 和 75 名 BD)时表现出良好的性能(AUC = 0.83)。随后,该模型在无药物治疗的 MDD 与 BD(11 名 MDD 和 10 名 BD)之间的表现也非常出色(AUC = 0.96),在 MDD 与 HC(AUC = 0.87)和 BD 与 HC(AUC = 0.86)之间的表现也相当出色。此外,这九个蛋白质与神经、氧化/硝化应激和免疫/炎症相关的生物学功能有关。本概念验证研究介绍了一种用于区分这两种疾病的潜在模型。