Potential interactions between cerebellar dysfunction and sleep disturbances in dystonia.

Dystonia Pub Date : 2022-10-01 Epub Date: 2022-10-04 DOI:10.3389/dyst.2022.10691
Luis E Salazar Leon, Roy V Sillitoe
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Abstract

Dystonia is the third most common movement disorder. It causes debilitating twisting postures that are accompanied by repetitive and sometimes intermittent co- or over-contractions of agonist and antagonist muscles. Historically diagnosed as a basal ganglia disorder, dystonia is increasingly considered a network disorder involving various brain regions including the cerebellum. In certain etiologies of dystonia, aberrant motor activity is generated in the cerebellum and the abnormal signals then propagate through a "dystonia circuit" that includes the thalamus, basal ganglia, and cerebral cortex. Importantly, it has been reported that non-motor defects can accompany the motor symptoms; while their severity is not always correlated, it is hypothesized that common pathways may nevertheless be disrupted. In particular, circadian dysfunction and disordered sleep are common non-motor patient complaints in dystonia. Given recent evidence suggesting that the cerebellum contains a circadian oscillator, displays sleep-stage-specific neuronal activity, and sends robust long-range projections to several subcortical regions involved in circadian rhythm regulation, disordered sleep in dystonia may result from cerebellum-mediated dysfunction of the dystonia circuit. Here, we review the evidence linking dystonia, cerebellar network dysfunction, and cerebellar involvement in sleep. Together, these ideas may form the basis for the development of improved pharmacological and surgical interventions that could take advantage of cerebellar circuitry to restore normal motor function as well as non-motor (sleep) behaviors in dystonia.

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肌张力障碍中小脑功能障碍和睡眠障碍之间的潜在相互作用。
肌张力障碍是第三大常见运动障碍。肌张力障碍是第三种最常见的运动障碍,会导致患者出现令人衰弱的扭曲姿势,并伴有激动肌和拮抗肌的重复性、有时是间歇性的共同或过度收缩。肌张力障碍历来被诊断为基底节障碍,但现在越来越多的人认为它是一种涉及包括小脑在内的多个脑区的网络性障碍。在肌张力障碍的某些病因中,小脑会产生异常的运动活动,然后异常信号会通过 "肌张力障碍回路 "传播,该回路包括丘脑、基底节和大脑皮层。重要的是,据报道,非运动缺陷可能伴随着运动症状;虽然它们的严重程度并不总是相关,但据推测,共同的通路可能受到了干扰。尤其是,昼夜节律失调和睡眠紊乱是肌张力障碍患者常见的非运动症状。最近有证据表明,小脑含有昼夜节律振荡器,显示睡眠阶段特异性神经元活动,并向多个参与昼夜节律调节的皮层下区域发出强大的长程投射,因此肌张力障碍患者的睡眠障碍可能是小脑介导的肌张力障碍回路功能障碍所致。在此,我们回顾了将肌张力障碍、小脑网络功能障碍和小脑参与睡眠联系起来的证据。这些观点合在一起,可能会为开发更好的药物和手术干预措施奠定基础,从而利用小脑回路恢复肌张力障碍患者的正常运动功能和非运动(睡眠)行为。
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