Wang Xuyang, Yoo Kwangsun, Chen Huafu, Zou Ting, Wang Hongyu, Gao Qing, Meng Li, Hu Xiaofei, Li Rong
The Clinical Hospital of Chengdu Brain Science Institute, MOE Key Laboratory for Neuroinformation, High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China.
Department of Psychology, Yale University, New Haven, CT, 06520, USA.
NPJ Parkinsons Dis. 2022 Apr 22;8(1):49. doi: 10.1038/s41531-022-00315-w.
Motor impairment is a core clinical feature of Parkinson's disease (PD). Although the decoupled brain connectivity has been widely reported in previous neuroimaging studies, how the functional connectome is involved in motor dysfunction has not been well elucidated in PD patients. Here we developed a distributed brain signature by predicting clinical motor scores of PD patients across multicenter datasets (total n = 236). We decomposed the Pearson's correlation into accordance and discordance via a temporal discrete procedure, which can capture coupling and anti-coupling respectively. Using different profiles of functional connectivity, we trained candidate predictive models and tested them on independent and heterogeneous PD samples. We showed that the antagonistic model measured by discordance had the best sensitivity and generalizability in all validations and it was dubbed as Parkinson's antagonistic motor signature (PAMS). The PAMS was dominated by the subcortical, somatomotor, visual, cerebellum, default-mode, and frontoparietal networks, and the motor-visual stream accounted for the most part of predictive weights among network pairs. Additional stage-specific analysis showed that the predicted scores generated from the antagonistic model tended to be higher than the observed scores in the early course of PD, indicating that the functional signature may vary more sensitively with the neurodegenerative process than clinical behaviors. Together, these findings suggest that motor dysfunction of PD is represented as antagonistic interactions within multi-level brain systems. The signature shows great potential in the early motor evaluation and developing new therapeutic approaches for PD in the clinical realm.
运动功能障碍是帕金森病(PD)的核心临床特征。尽管在先前的神经影像学研究中已广泛报道了解耦的脑连接性,但在PD患者中,功能连接组如何参与运动功能障碍尚未得到充分阐明。在此,我们通过预测多中心数据集中PD患者的临床运动评分(总计n = 236),开发了一种分布式脑特征。我们通过时间离散程序将皮尔逊相关性分解为一致性和不一致性,分别可以捕获耦合和反耦合。使用不同的功能连接配置文件,我们训练了候选预测模型,并在独立且异质的PD样本上对其进行测试。我们表明,由不一致性测量的拮抗模型在所有验证中具有最佳的敏感性和通用性,并被称为帕金森拮抗运动特征(PAMS)。PAMS由皮质下、躯体运动、视觉、小脑、默认模式和额顶叶网络主导,并且运动-视觉流在网络对之间的预测权重中占大部分。额外的阶段特异性分析表明,在PD病程早期,由拮抗模型生成的预测评分往往高于观察到的评分,这表明功能特征可能比临床行为更敏感地随神经退行性过程而变化。总之,这些发现表明PD的运动功能障碍表现为多级脑系统内的拮抗相互作用。该特征在临床领域的早期运动评估和开发PD新治疗方法方面显示出巨大潜力。