McClelland Verity M, Lin Jean-Pierre
Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
Children's Neurosciences Department, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Front Neurol. 2021 Jul 23;12:668081. doi: 10.3389/fneur.2021.668081. eCollection 2021.
Dystonia is a disorder of sensorimotor integration, involving dysfunction within the basal ganglia, cortex, cerebellum, or their inter-connections as part of the sensorimotor network. Some forms of dystonia are also characterized by maladaptive or exaggerated plasticity. Development of the neuronal processes underlying sensorimotor integration is incompletely understood but involves activity-dependent modeling and refining of sensorimotor circuits through processes that are already taking place and which continue through infancy, childhood, and into adolescence. Several genetic dystonias have clinical onset in early childhood, but there is evidence that sensorimotor circuit development may already be disrupted prenatally in these conditions. Dystonic cerebral palsy (DCP) is a form of acquired dystonia with perinatal onset during a period of rapid neurodevelopment and activity-dependent refinement of sensorimotor networks. However, physiological studies of children with dystonia are sparse. This discussion paper addresses the role of neuroplasticity in the development of sensorimotor integration with particular focus on the relevance of these mechanisms for understanding childhood dystonia, DCP, and implications for therapy selection, including neuromodulation and timing of intervention.
肌张力障碍是一种感觉运动整合障碍,涉及基底神经节、皮质、小脑或它们作为感觉运动网络一部分的相互连接中的功能障碍。某些形式的肌张力障碍还具有适应不良或过度可塑性的特征。感觉运动整合背后的神经元过程的发展尚未完全了解,但涉及通过已经发生且贯穿婴儿期、儿童期直至青春期的过程对感觉运动回路进行活动依赖性建模和优化。几种遗传性肌张力障碍在幼儿期临床发病,但有证据表明在这些情况下感觉运动回路的发育可能在产前就已受到破坏。肌张力障碍型脑瘫(DCP)是一种获得性肌张力障碍,在神经快速发育和感觉运动网络活动依赖性优化的时期围产期发病。然而,对肌张力障碍儿童的生理学研究很少。这篇讨论文章探讨了神经可塑性在感觉运动整合发展中的作用,特别关注这些机制对于理解儿童肌张力障碍、DCP的相关性以及对治疗选择的影响,包括神经调节和干预时机。