Grimm Kai, Sadeghi Fatemeh, Schön Gerhard, Okar Abdullah, Gelderblom Mathias, Schulz Robert, Zittel Simone
Department of Neurology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany.
Institute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
J Neural Transm (Vienna). 2025 Feb;132(2):257-264. doi: 10.1007/s00702-024-02839-2. Epub 2024 Oct 7.
Recently, a network model of cervical dystonia (CD) has been adopted that implicates nodes and pathways involving cerebellar, basal-ganglia and cortico-cortical connections. Although functional changes in the cerebello-thalamo-cortical network in dystonia have been reported in several studies, structural information of this network remain sparse.
To characterize the structural properties of the cerebellar motor network in isolated CD patients. This includes cerebellar lobules involved in motor processing, the dentate nucleus (DN), the thalamus, and the primary motor cortex (M1).
Magnetic resonance imaging data of 18 CD patients and 18 healthy control subjects were acquired. In CD patients, the motor part of the Toronto Western Spasmodic Torticollis Rating Scale was assessed to evaluate motor symptom severity. The volume of cerebellar lobules I-VI and VIII, the DN and thalamus, and the cortical thickness (CT) of M1 were determined for a region of interest (ROI)-based quantitative analysis. Volumes/CT of these ROIs were compared between groups and associated with motor symptom severity in patients.
The volume of lobule VI and the CT of M1 were reduced in CD patients. The volumes of the other ROIs were not different between groups. No association was identified between the structural properties of lobule VI or M1 and the severity of CD motor symptoms.
Atrophy within the cerebellum and M1 contributes to CD's complex motor network pathology. Further investigations are needed to ascertain the mechanisms underlying the local volume loss.
最近,一种颈肌张力障碍(CD)的网络模型被采用,该模型涉及小脑、基底神经节和皮质-皮质连接的节点及通路。尽管多项研究报道了肌张力障碍患者小脑-丘脑-皮质网络的功能变化,但该网络的结构信息仍然匮乏。
描述孤立性CD患者小脑运动网络的结构特性。这包括参与运动处理的小脑小叶、齿状核(DN)、丘脑和初级运动皮层(M1)。
获取了18例CD患者和18名健康对照者的磁共振成像数据。在CD患者中,评估了多伦多西部痉挛性斜颈评定量表的运动部分,以评估运动症状的严重程度。基于感兴趣区域(ROI)的定量分析确定了小脑小叶I-VI和VIII、DN和丘脑的体积以及M1的皮质厚度(CT)。比较了两组之间这些ROI的体积/CT,并将其与患者的运动症状严重程度相关联。
CD患者的小叶VI体积和M1的CT降低。两组之间其他ROI的体积没有差异。未发现小叶VI或M1的结构特性与CD运动症状严重程度之间存在关联。
小脑和M1内的萎缩导致了CD复杂的运动网络病理。需要进一步研究以确定局部体积损失的潜在机制。