Burciu Roxana G, Hess Christopher W, Coombes Stephen A, Ofori Edward, Shukla Priyank, Chung Jae Woo, McFarland Nikolaus R, Wagle Shukla Aparna, Okun Michael S, Vaillancourt David E
Department of Applied Physiology and Kinesiology, University of Florida, Gainesville, Florida.
Department of Neurology, University of Florida, Gainesville, Florida.
Hum Brain Mapp. 2017 Sep;38(9):4563-4573. doi: 10.1002/hbm.23684. Epub 2017 Jun 8.
Cervical dystonia (CD) is the most common type of focal dystonia, causing abnormal movements of the neck and head. In this study, we used noninvasive imaging to investigate the motor system of patients with CD and uncover the neural correlates of dystonic symptoms. Furthermore, we examined whether a commonly prescribed anticholinergic medication in CD has an effect on the dystonia-related brain abnormalities. Participants included 16 patients with CD and 16 healthy age-matched controls. We collected functional MRI scans during a force task previously shown to extensively engage the motor system, and diffusion and T1-weighted MRI scans from which we calculated free-water and brain tissue densities. The dystonia group was also scanned ca. 2 h after a 2-mg dose of trihexyphenidyl. Severity of dystonia was assessed pre- and post-drug using the Burke-Fahn-Marsden Dystonia Rating Scale. Motor-related activity in CD was altered relative to controls in the primary somatosensory cortex, cerebellum, dorsal premotor and posterior parietal cortices, and occipital cortex. Most importantly, a regression model showed that increased severity of symptoms was associated with decreased functional activity of the somatosensory cortex and increased activity of the cerebellum. Structural imaging measures did not differ between CD and controls. The single dose of trihexyphenidyl altered the fMRI signal in the somatosensory cortex but not in the cerebellum. Symptom severity was not significantly reduced post-treatment. Findings show widespread changes in functional brain activity in CD and most importantly that dystonic symptoms relate to disrupted activity in the somatosensory cortex and cerebellum. Hum Brain Mapp 38:4563-4573, 2017. © 2017 Wiley Periodicals, Inc.
颈部肌张力障碍(CD)是最常见的局限性肌张力障碍类型,可导致颈部和头部的异常运动。在本研究中,我们使用非侵入性成像技术来研究CD患者的运动系统,并揭示肌张力障碍症状的神经关联。此外,我们还研究了CD中常用的抗胆碱能药物是否对与肌张力障碍相关的脑异常有影响。参与者包括16例CD患者和16名年龄匹配的健康对照者。我们在一项先前已证明能广泛激活运动系统的力量任务期间收集了功能磁共振成像扫描数据,以及扩散加权成像和T1加权磁共振成像扫描数据,从中计算出自由水和脑组织密度。肌张力障碍组在服用2毫克苯海索后约2小时也进行了扫描。使用伯克 - 法恩 - 马斯登肌张力障碍评定量表在用药前后评估肌张力障碍的严重程度。与对照组相比,CD患者在初级体感皮层、小脑、背侧运动前区和顶叶后皮质以及枕叶皮质的运动相关活动发生了改变。最重要的是,回归模型显示症状严重程度增加与体感皮层功能活动降低以及小脑活动增加有关。CD组和对照组之间的结构成像测量结果没有差异。单剂量的苯海索改变了体感皮层的功能磁共振成像信号,但未改变小脑的信号。治疗后症状严重程度没有显著降低。研究结果表明,CD患者脑功能活动存在广泛变化,最重要的是,肌张力障碍症状与体感皮层和小脑的活动紊乱有关。《人类大脑图谱》38:4563 - 4573, 2017。© 2017威利期刊公司。