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Multimodal Quantitative MRI Reveals No Evidence for Tissue Pathology in Idiopathic Cervical Dystonia

机译:多模式定量MRI未发现特发性宫颈肌张力障碍的组织病理学证据

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摘要

>Background: While in symptomatic forms of dystonia cerebral pathology is by definition present, it is unclear so far whether disease is associated with microstructural cerebral changes in idiopathic dystonia. Previous quantitative MRI (qMRI) studies assessing cerebral tissue composition in idiopathic dystonia revealed conflicting results.>Objective: Using multimodal qMRI, the presented study aimed to investigate alterations in different cerebral microstructural compartments associated with idiopathic cervical dystonia in vivo.>Methods: Mapping of T1, T2, T2*, and proton density (PD) was performed in 17 patients with idiopathic cervical dystonia and 29 matched healthy control subjects. Statistical comparisons of the parametric maps between groups were conducted for various regions of interest (ROI), including major basal ganglia nuclei, the thalamus, white matter, and the cerebellum, and voxel-wise for the whole brain.>Results: Neither whole brain voxel-wise statistics nor ROI-based analyses revealed significant group differences for any qMRI parameter under investigation.>Conclusions: The negative findings of this qMRI study argue against the presence of overt microstructural tissue change in patients with idiopathic cervical dystonia. The results seem to support a common view that idiopathic cervical dystonia might primarily resemble a functional network disease.
机译:>背景:虽然按照症状形式的肌张力障碍存在脑病理学,但目前尚不清楚疾病是否与特发性肌张力障碍的微结构脑变有关。先前的定量MRI(qMRI)研究评估了特发性肌张力障碍的脑组织组成,发现了相互矛盾的结果。>目的:本研究使用多峰qMRI旨在研究与特发性宫颈肌张力障碍相关的不同脑微结构区室的变化。>方法:映射T1,T2和 T 2 * 结果:< / strong>全脑体素统计或基于ROI的分析均未显示所调查的任何qMRI参数的显着组差异。>结论:该qMRI研究的阴性结果表明存在明显的显微组织特发性颈肌张力障碍患者的改变。该结果似乎支持一个普遍的观点,即特发性宫颈肌张力障碍可能主要类似于功能性网络疾病。

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