Berman Brian D, Pollard Rebecca Tran, Shelton Erika, Karki Ramesh, Smith-Jones Peter M, Miao Yubin
Department of Neurology, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Department of Radiology, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Front Neurol. 2018 Apr 4;9:188. doi: 10.3389/fneur.2018.00188. eCollection 2018.
GABA receptor availability changes within sensorimotor regions have been reported in some isolated forms of dystonia. Whether similar abnormalities underlie symptoms in cervical dystonia is not known. In the present study, a total of 15 cervical dystonia patients and 15 age- and sex-matched controls underwent C-flumazenil PET/CT scanning. The density of available GABA receptors was estimated using a Simplified Reference Tissue Model 2. Group differences were evaluated using a two-sample -test, and correlations with dystonia severity, as measured by the Toronto Western Spasmodic Torticollis Rating Scale, and disease duration were evaluated using a regression analysis. Voxel-based analyses revealed increased GABA availability within the right precentral gyrus in brain motor regions previously associated with head turning and the left parahippocampal gyrus. GABA availability within the bilateral cerebellum was negatively correlated with dystonia severity, and GABA availability within the right thalamus and a variety of cerebellar and cortical regions were negatively correlated with disease duration. While GABA availability changes within primary motor areas could represent a partial compensatory response to loss of inhibition within sensorimotor network, GABAergic signaling impairment within the cerebellum may be a key contributor to dystonia severity.
在一些孤立形式的肌张力障碍中,已报道感觉运动区域内GABA受体可用性发生变化。颈肌张力障碍症状是否存在类似异常尚不清楚。在本研究中,共有15例颈肌张力障碍患者和15例年龄及性别匹配的对照者接受了C-氟马西尼PET/CT扫描。使用简化参考组织模型2估计可用GABA受体的密度。使用两样本t检验评估组间差异,并使用回归分析评估与肌张力障碍严重程度(通过多伦多西部痉挛性斜颈评定量表测量)和病程的相关性。基于体素的分析显示,在先前与头部转动相关的脑运动区域右中央前回以及左海马旁回中,GABA可用性增加。双侧小脑中的GABA可用性与肌张力障碍严重程度呈负相关,右丘脑中的GABA可用性以及各种小脑和皮质区域中的GABA可用性与病程呈负相关。虽然初级运动区域内GABA可用性变化可能代表对感觉运动网络内抑制丧失的部分代偿反应,但小脑中的GABA能信号传导受损可能是肌张力障碍严重程度的关键因素。