Eisenstein Sarah A, Koller Jonathan M, Black Kathleen D, Campbell Meghan C, Lugar Heather M, Ushe Mwiza, Tabbal Samer D, Karimi Morvarid, Hershey Tamara, Perlmutter Joel S, Black Kevin J
Department of Psychiatry, Washington University in St Louis, St Louis, MO.
Ann Neurol. 2014 Aug;76(2):279-95. doi: 10.1002/ana.24204. Epub 2014 Jul 2.
We developed a novel method to map behavioral effects of deep brain stimulation (DBS) across a 3-dimensional brain region and to assign statistical significance after stringent type I error correction. This method was applied to behavioral changes in Parkinson disease (PD) induced by subthalamic nucleus (STN) DBS to determine whether these responses depended on anatomical location of DBS.
Fifty-one PD participants with STN DBS were evaluated off medication, with DBS off and during unilateral STN DBS with clinically optimized settings. Dependent variables included DBS-induced changes in Unified Parkinson Disease Rating Scale (UPDRS) subscores, kinematic measures of bradykinesia and rigidity, working memory, response inhibition, mood, anxiety, and akathisia. Weighted t tests at each voxel produced p images showing where DBS most significantly affected each dependent variable based on outcomes of participants with nearby DBS. Finally, a permutation test computed the probability that this p image indicated significantly different responses based on stimulation site.
Most motor variables improved with DBS anywhere in the STN region, but several motor, cognitive, and affective responses significantly depended on precise location stimulated, with peak p values in superior STN/zona incerta (quantified bradykinesia), dorsal STN (mood, anxiety), and inferior STN/substantia nigra (UPDRS tremor, working memory).
Our method identified DBS-induced behavioral changes that depended significantly on DBS site. These results do not support complete functional segregation within STN, because movement improved with DBS throughout, and mood improved with dorsal STN DBS. Rather, findings support functional convergence of motor, cognitive, and limbic information in STN.
我们开发了一种新方法,用于在三维脑区绘制深部脑刺激(DBS)的行为效应,并在严格的I型错误校正后确定统计学意义。该方法应用于丘脑底核(STN)DBS诱发的帕金森病(PD)行为变化,以确定这些反应是否依赖于DBS的解剖位置。
对51名接受STN DBS的PD患者在停药状态下、DBS关闭时以及单侧STN DBS且临床设置优化期间进行评估。因变量包括DBS诱发的统一帕金森病评定量表(UPDRS)子评分变化、运动迟缓与僵硬的运动学测量、工作记忆、反应抑制、情绪、焦虑和静坐不能。在每个体素处进行加权t检验,生成p图像,显示基于附近DBS参与者的结果,DBS对每个因变量影响最显著的位置。最后,通过置换检验计算该p图像基于刺激部位显示显著不同反应的概率。
STN区域内任何位置进行DBS时,大多数运动变量都有所改善,但一些运动、认知和情感反应显著依赖于精确的刺激位置,在STN上部/未定带(定量运动迟缓)、STN背侧(情绪、焦虑)以及STN下部/黑质(UPDRS震颤、工作记忆)处达到p值峰值。
我们的方法识别出了显著依赖于DBS部位的DBS诱发的行为变化。这些结果不支持STN内完全的功能分离,因为整个STN进行DBS时运动均得到改善,且STN背侧进行DBS时情绪得到改善。相反,研究结果支持STN中运动、认知和边缘系统信息的功能汇聚。