Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.
Lysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, UCLH NHS Foundation Trust, London, WC1N 3BG, UK.
Brain. 2019 Aug 1;142(8):2417-2431. doi: 10.1093/brain/awz164.
Subthalamic nucleus deep brain stimulation is an effective treatment for advanced Parkinson's disease; however, its therapeutic mechanism is unclear. Previous modelling of functional MRI data has suggested that deep brain stimulation has modulatory effects on a number of basal ganglia pathways. This work uses an enhanced data collection protocol to collect rare functional MRI data in patients with subthalamic nucleus deep brain stimulation. Eleven patients with Parkinson's disease and subthalamic nucleus deep brain stimulation underwent functional MRI at rest and during a movement task; once with active deep brain stimulation, and once with deep brain stimulation switched off. Dynamic causal modelling and Bayesian model selection were first used to compare a series of plausible biophysical models of the cortico-basal ganglia circuit that could explain the functional MRI activity at rest in an attempt to reproduce and extend the findings from our previous work. General linear modelling of the movement task functional MRI data revealed deep brain stimulation-associated signal increases in the primary motor and cerebellar cortices. Given the significance of the cerebellum in voluntary movement, we then built a more complete model of the motor system by including cerebellar-basal ganglia interactions, and compared the modulatory effects deep brain stimulation had on different circuit components during the movement task and again using the resting state data. Consistent with previous results from our independent cohort, model comparison found that the rest data were best explained by deep brain stimulation-induced increased (effective) connectivity of the cortico-striatal, thalamo-cortical and direct pathway and reduced coupling of subthalamic nucleus afferent and efferent connections. No changes in cerebellar connectivity were identified at rest. In contrast, during the movement task, there was functional recruitment of subcortical-cerebellar pathways, which were additionally modulated by deep brain stimulation, as well as modulation of local (intrinsic) cortical and cerebellar circuits. This work provides in vivo evidence for the modulatory effects of subthalamic nucleus deep brain stimulation on effective connectivity within the cortico-basal ganglia loops at rest, as well as further modulations in the cortico-cerebellar motor system during voluntary movement. We propose that deep brain stimulation has both behaviour-independent effects on basal ganglia connectivity, as well as behaviour-dependent modulatory effects.
丘脑底核深部脑刺激是治疗晚期帕金森病的有效方法;然而,其治疗机制尚不清楚。先前对功能磁共振成像数据的建模表明,深部脑刺激对许多基底节通路具有调节作用。这项工作使用增强的数据采集协议来收集接受丘脑底核深部脑刺激的患者的罕见功能磁共振成像数据。11 名帕金森病患者和丘脑底核深部脑刺激接受了静息和运动任务期间的功能磁共振成像;一次是在深部脑刺激激活时,一次是在深部脑刺激关闭时。首先使用动态因果建模和贝叶斯模型选择来比较皮质基底节回路的一系列合理的生物物理模型,这些模型可以解释静息状态下的功能磁共振成像活动,试图复制和扩展我们之前工作的发现。运动任务功能磁共振成像数据的广义线性建模显示深部脑刺激与初级运动和小脑皮质相关的信号增加。鉴于小脑在自主运动中的重要性,我们通过包括小脑-基底节相互作用,构建了一个更完整的运动系统模型,并使用静息状态数据再次比较深部脑刺激在运动任务期间对不同回路组件的调节作用。与我们独立队列的先前结果一致,模型比较发现,休息数据最好通过深部脑刺激诱导的皮质-纹状体、丘脑-皮质和直接通路的增强(有效)连接以及减少丘脑底核传入和传出连接的耦合来解释。在休息时未发现小脑连接的变化。相比之下,在运动任务期间,存在亚皮质-小脑通路的功能募集,深部脑刺激进一步调节这些通路,以及局部(内在)皮质和小脑回路的调节。这项工作提供了体内证据,证明了在静息状态下,丘脑底核深部脑刺激对皮质-基底节回路的有效连接具有调节作用,以及在自主运动期间对皮质-小脑运动系统的进一步调节。我们提出,深部脑刺激对基底节连接既有行为独立的影响,也有行为依赖的调节作用。