Department of Clinical, Neuro- and Developmental Psychology, Faculty of Behavior- and Movement Sciences, VU University, Van der Boechorststraat 1, 1081 BT, Amsterdam, The Netherlands.
Department of Experimental and Applied Psychology & Institute of Brain and Behavior Amsterdam, Faculty of Behavior- and Movement Sciences, VU University, Van der Boechorststraat 1, Amsterdam, The Netherlands.
J Neural Transm (Vienna). 2018 Oct;125(10):1449-1459. doi: 10.1007/s00702-018-1916-y. Epub 2018 Aug 21.
Pain is an important non-motor symptom in Parkinson's disease (PD), but its underlying pathophysiological mechanisms are still unclear. Research has shown that functional connectivity during the resting-state may be involved in persistent pain in PD. In the present cross-sectional study, 24 PD patients (both during on and off medication phase) and 27 controls participated. We assessed pain with the colored analogue scale and the McGill pain questionnaire. We examined a possible pathophysiological mechanism with resting-state fMRI using functional network topology, i.e., the architecture of functional connections. We took betweenness centrality (BC) to assess hubness, and global efficiency (GE) to assess integration of the network. We aimed to (1) assess the differences between PD patients and controls with respect to pain and resting-state network topology, and (2) investigate how resting-state network topology (BC and GE) is associated with clinical pain in both PD patients and controls. Results show that PD patients experienced more pain than controls. GE of the whole brain was higher in PD patients (on as well as off medication) compared to healthy controls. GE of the specialized pain network was also higher in PD patients compared to controls, but only when patients were on medication. BC of the pain network was lower in PD patients off medication compared to controls. We found a positive association between pain and GE of the pain network in PD patients off medication. For healthy controls, a negative association was found between pain and GE of the pain network, and also between pain and BC of the pain network. Our results suggest that functional network topology differs between PD patients and healthy controls, and that this topology can be used to investigate the underlying neural mechanisms of pain symptoms in PD.
疼痛是帕金森病(PD)的重要非运动症状,但其潜在的病理生理机制仍不清楚。研究表明,静息状态下的功能连接可能与 PD 患者的持续性疼痛有关。在本横断面研究中,共有 24 名 PD 患者(包括服药期和停药期)和 27 名对照者参与。我们使用彩色模拟量表和麦吉尔疼痛问卷评估疼痛。我们使用静息态 fMRI 检查了功能网络拓扑(即功能连接的结构)的可能病理生理机制。我们采用介数中心度(BC)评估枢纽度,采用全局效率(GE)评估网络的整合度。我们旨在:(1)评估 PD 患者和对照组在疼痛和静息态网络拓扑方面的差异;(2)研究静息态网络拓扑(BC 和 GE)与 PD 患者和对照组的临床疼痛之间的关系。结果显示,PD 患者的疼痛程度高于对照组。与健康对照组相比,PD 患者(服药期和停药期)的全脑 GE 更高。与对照组相比,PD 患者的专门疼痛网络的 GE 也更高,但仅在患者服药时如此。与对照组相比,PD 患者停药时的疼痛网络 BC 较低。我们发现 PD 患者停药时疼痛与疼痛网络的 GE 之间呈正相关。对于健康对照组,疼痛与疼痛网络的 GE 之间呈负相关,疼痛与疼痛网络的 BC 之间也呈负相关。我们的研究结果表明,PD 患者和健康对照组之间的功能网络拓扑存在差异,并且这种拓扑可以用于研究 PD 患者疼痛症状的潜在神经机制。