Chen Yen-Ling, Huang Tzu-Hsuan, Tu Pei-Chi, Bai Ya-Mei, Su Tung-Ping, Chen Mu-Hong, Hong Jia-Sheng, Wu Yu-Te
Department of Occupational Therapy, I-Shou University, Kaohsiung 840, Taiwan.
Institute of Biophotonics, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Biomedicines. 2022 Nov 25;10(12):3047. doi: 10.3390/biomedicines10123047.
Predictive neurobiological markers for prognosis are essential but underemphasized for patients with bipolar disorder (BD), a neuroprogressive disorder. Hence, we developed models for predicting symptom and functioning changes. Sixty-one patients with BD were recruited and assessed using the Young Mania Rating Scale (YMRS), Montgomery−Åsberg Depression Rating Scale (MADRS), Positive and Negative Syndrome Scale (PANSS), UKU Side Effect Rating Scale (UKU), Personal and Social Performance Scale (PSP), and Global Assessment of Functioning scale both at baseline and after 1-year follow-up. The models for predicting the changes in symptom and functioning scores were trained using data on the brain morphology, functional connectivity, and cytokines collected at baseline. The correlation between the predicted and actual changes in the YMRS, MADRS, PANSS, and UKU scores was higher than 0.86 (q < 0.05). Connections from subcortical and cerebellar regions were considered for predicting the changes in the YMRS, MADRS, and UKU scores. Moreover, connections of the motor network were considered for predicting the changes in the YMRS and MADRS scores. The neurobiological markers for predicting treatment-response symptoms and functioning changes were consistent with the neuropathology of BD and with the differences found between treatment responders and nonresponders.
对于双相情感障碍(BD)这种神经退行性疾病的患者而言,预测预后的神经生物学标志物至关重要,但却未得到足够重视。因此,我们开发了用于预测症状和功能变化的模型。招募了61名BD患者,并在基线期和1年随访后使用杨氏躁狂评定量表(YMRS)、蒙哥马利-阿斯伯格抑郁评定量表(MADRS)、阳性和阴性症状量表(PANSS)、UKU副作用评定量表(UKU)、个人和社会表现量表(PSP)以及功能总体评定量表进行评估。利用基线期收集的脑形态学、功能连接和细胞因子数据,训练预测症状和功能评分变化的模型。YMRS、MADRS、PANSS和UKU评分的预测变化与实际变化之间的相关性高于0.86(q < 0.05)。在预测YMRS、MADRS和UKU评分变化时考虑了来自皮质下和小脑区域的连接。此外,在预测YMRS和MADRS评分变化时考虑了运动网络的连接。预测治疗反应症状和功能变化的神经生物学标志物与BD的神经病理学以及治疗反应者和无反应者之间的差异一致。