National Engineering Laboratory for Neuromodulation, School of Aerospace Engineering, Tsinghua University, Beijing, China.
Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.
Ann Neurol. 2020 Dec;88(6):1178-1193. doi: 10.1002/ana.25906. Epub 2020 Oct 13.
Current understanding of the neuromodulatory effects of deep brain stimulation (DBS) on large-scale brain networks remains elusive, largely due to the lack of techniques that can reveal DBS-induced activity at the whole-brain level. Using a novel 3T magnetic resonance imaging (MRI)-compatible stimulator, we investigated whole-brain effects of subthalamic nucleus (STN) stimulation in patients with Parkinson disease.
Fourteen patients received STN-DBS treatment and participated in a block-design functional MRI (fMRI) experiment, wherein stimulations were delivered during "ON" blocks interleaved with "OFF" blocks. fMRI responses to low-frequency (60Hz) and high-frequency(130Hz) STN-DBS were measured 1, 3, 6, and 12 months postsurgery. To ensure reliability, multiple runs (48 minutes) of fMRI data were acquired at each postsurgical visit. Presurgical resting-state fMRI (30 minutes) data were also acquired.
Two neurocircuits showed highly replicable, but distinct responses to STN-DBS. A circuit involving the globus pallidus internus (GPi), thalamus, and deep cerebellar nuclei was significantly activated, whereas another circuit involving the primary motor cortex (M1), putamen, and cerebellum showed DBS-induced deactivation. These 2 circuits were dissociable in terms of their DBS-induced responses and resting-state functional connectivity. The GPi circuit was frequency-dependent, selectively responding to high-frequency stimulation, whereas the M1 circuit was responsive in a time-dependent manner, showing enhanced deactivation over time. Finally, activation of the GPi circuit was associated with overall motor improvement, whereas M1 circuit deactivation was related to reduced bradykinesia.
Concurrent DBS-fMRI using 3T revealed 2 distinct circuits that responded differentially to STN-DBS and were related to divergent symptoms, a finding that may provide novel insights into the neural mechanisms underlying DBS. ANN NEUROL 2020;88:1178-1193.
目前对于深部脑刺激(DBS)对大脑网络的神经调节作用的理解仍然难以捉摸,主要是因为缺乏可以揭示整个大脑水平 DBS 诱导活性的技术。使用新型 3T 磁共振成像(MRI)兼容刺激器,我们研究了帕金森病患者的丘脑底核(STN)刺激的全脑效应。
14 名患者接受 STN-DBS 治疗并参与了一项块设计功能磁共振成像(fMRI)实验,其中在“ON”块和“OFF”块之间插入刺激。在手术后 1、3、6 和 12 个月测量低频(60Hz)和高频(130Hz)STN-DBS 的 fMRI 反应。为了确保可靠性,在每次手术后就诊时都采集了多个(48 分钟)fMRI 数据运行。还采集了术前静息状态 fMRI(30 分钟)数据。
两个神经回路对 STN-DBS 表现出高度可复制但不同的反应。一个包括苍白球内(GPi)、丘脑和深部小脑核的回路明显被激活,而另一个包括初级运动皮层(M1)、壳核和小脑的回路显示出 DBS 诱导的失活。这两个回路在 DBS 诱导的反应和静息状态功能连接方面是可分离的。GPi 回路是频率依赖性的,选择性地对高频刺激作出反应,而 M1 回路则以时间依赖性的方式作出反应,随着时间的推移显示出增强的失活。最后,GPi 回路的激活与整体运动改善有关,而 M1 回路的失活与运动迟缓减少有关。
使用 3T 的同步 DBS-fMRI 揭示了 2 个不同的回路,它们对 STN-DBS 的反应不同,与不同的症状有关,这一发现可能为 DBS 背后的神经机制提供新的见解。ANN NEUROL 2020;88:1178-1193。