Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, USA.
Columbia University Medical Center, Department of Psychiatry, New York, New York, USA.
Mov Disord. 2017 Nov;32(11):1537-1545. doi: 10.1002/mds.27123. Epub 2017 Aug 26.
Dystonia is a common movement disorder that devastates the lives of many patients, but the etiology of this disorder remains poorly understood. Dystonia has traditionally been considered a disorder of the basal ganglia. However, growing evidence suggests that the cerebellum may be involved in certain types of dystonia, raising several questions. Can different types of dystonia be classified as either a basal ganglia disorder or a cerebellar disorder? Is dystonia a network disorder that involves the cerebellum and basal ganglia? If dystonia is a network disorder, how can we target treatments to alleviate symptoms in patients? A recent study by Chen et al, using the pharmacological mouse model of rapid-onset dystonia parkinsonism, has provided some insight into these important questions. They showed that the cerebellum can directly modulate basal ganglia activity through a short latency cerebello-thalamo-basal ganglia pathway. Further, this article and others have provided evidence that in some cases, aberrant cerebello-basal ganglia communication can be involved in dystonia. In this review we examine the evidence for the involvement of the cerebellum and cerebello-basal ganglia interactions in dystonia. We conclude that there is ample evidence to suggest that the cerebellum plays a role in some dystonias, including the early-onset primary torsion dystonia DYT1 and that further studies examining the role of this brain region and its interaction with the basal ganglia in dystonia are warranted. © 2017 International Parkinson and Movement Disorder Society.
肌张力障碍是一种常见的运动障碍疾病,严重影响许多患者的生活,但这种疾病的病因仍知之甚少。肌张力障碍传统上被认为是基底节疾病。然而,越来越多的证据表明,小脑可能参与某些类型的肌张力障碍,这引发了一些问题。不同类型的肌张力障碍能否被归类为基底节疾病或小脑疾病?肌张力障碍是一种涉及小脑和基底节的网络障碍吗?如果肌张力障碍是一种网络障碍,我们如何针对治疗以减轻患者的症状?陈等人最近的一项研究使用快速发作性肌张力障碍帕金森病的药理学小鼠模型,为这些重要问题提供了一些见解。他们表明,小脑可以通过短潜伏期小脑-丘脑-基底节通路直接调节基底节活动。此外,本文和其他研究提供的证据表明,在某些情况下,小脑-基底节通讯异常可能与肌张力障碍有关。在这篇综述中,我们检查了小脑和小脑-基底节相互作用在肌张力障碍中的作用的证据。我们的结论是,有充分的证据表明小脑在一些肌张力障碍中发挥作用,包括早发性原发性扭转性肌张力障碍 DYT1,进一步研究检查该脑区在肌张力障碍中的作用及其与基底节的相互作用是有必要的。 © 2017 国际帕金森病和运动障碍学会。