Sobell Department for Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, 33 Queen Square, London, WC1N 3BG, UK.
Motor Control and Movement Disorder Group, Institute of Molecular and Clinical Sciences, St George's University of London, Cranmer Terrace, Tooting, London, SW17 0RE, UK.
Sci Rep. 2018 Feb 26;8(1):3653. doi: 10.1038/s41598-018-21545-0.
For the healthy motor control system, an essential regulatory role is maintaining the equilibrium between keeping unwanted motor variability in check whilst allowing informative elements of motor variability. Kinematic studies in children with generalised dystonia (due to mixed aetiologies) show that movements are characterised by increased motor variability. In this study, the mechanisms by which high motor variability may influence movement generation in dystonia were investigated. Reaching movements in the symptomatic arm of 10 patients with DYT1 dystonia and 12 age-matched controls were captured using a robotic manipulandum and features of motor variability were extracted. Given that task-relevant variability and sensorimotor adaptation are related in health, markers of variability were then examined for any co-variance with performance indicators during an error-based learning visuomotor adaptation task. First, we confirmed that motor variability on a trial-by-trial basis was selectively increased in the homogenous and prototypical dystonic disorder DYT1 dystonia. Second, high baseline variability predicted poor performance in the subsequent visuomotor adaptation task offering insight into the rules which appear to govern dystonic motor control. The potential mechanisms behind increased motor variability and its corresponding implications for the rehabilitation of patients with DYT1 dystonia are highlighted.
对于健康的运动控制系统,一个重要的调节作用是在控制不必要的运动变异性的同时,保持运动变异性的信息元素。对广泛性肌张力障碍儿童(由于混合病因)的运动学研究表明,运动的特点是运动变异性增加。在这项研究中,研究了高运动变异性可能影响肌张力障碍运动产生的机制。使用机器人操纵器捕获了 10 名 DYT1 肌张力障碍患者和 12 名年龄匹配的对照者的症状性手臂的伸展运动,并提取了运动变异性的特征。鉴于健康状态下任务相关变异性和感觉运动适应之间存在相关性,因此在基于错误的视觉运动适应任务中,检查了变异性标志物与性能指标之间的任何协方差。首先,我们证实,在同质性和典型的肌张力障碍 DYT1 肌张力障碍中,逐次试验的运动变异性选择性增加。其次,高基线变异性预测随后的视觉运动适应任务表现不佳,为了解支配肌张力障碍运动控制的规则提供了线索。突出了运动变异性增加的潜在机制及其对 DYT1 肌张力障碍患者康复的相应影响。