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相位锁定经颅电刺激治疗肌张力障碍性震颤综合征的震颤。

Phase-locked transcranial electrical brain stimulation for tremor suppression in dystonic tremor syndromes.

机构信息

Centre for Cognitive Neuroimaging, Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands.

Department of Neurology and Clinical Neurophysiology, Amsterdam University Medical Centers, Amsterdam Neuroscience, University of Amsterdam, Amsterdam, the Netherlands.

出版信息

Clin Neurophysiol. 2022 Aug;140:239-250. doi: 10.1016/j.clinph.2022.03.020. Epub 2022 Apr 7.

Abstract

OBJECTIVE

To establish the causal role of the cerebellum and motor cortex in dystonic tremor syndromes, and explore the therapeutic efficacy of phase-locked transcranial alternating current stimulation (TACS).

METHODS

We applied phase-locked TACS over the ipsilateral cerebellum (N = 14) and contralateral motor cortex (N = 17) in dystonic tremor syndrome patients, while patients assumed a tremor-evoking posture. We measured tremor power using accelerometery during 30 s stimulation periods at 10 different phase-lags (36-degrees increments) between tremor and TACS for each target. Post-hoc, TACS-effects were related to a key clinical feature: the jerkiness (regularity) of tremor.

RESULTS

Cerebellar TACS modulated tremor amplitude in a phase-dependent manner, such that tremor amplitude was suppressed or enhanced at opposite sides of the phase-cycle. This effect was specific for patients with non-jerky (sinusoidal) tremor (n = 10), but absent in patients with jerky (irregular) tremor (n = 4). Phase-locked stimulation over the motor cortex did not modulate tremor amplitude.

CONCLUSIONS

This study indicates that the cerebellum plays a causal role in the generation of (non-jerky) dystonic tremor syndrome. Our findings suggest pathophysiologic heterogeneity between patients with dystonic tremor syndrome, which mirrors clinical variability.

SIGNIFICANCE

We show tremor phenotype dependent involvement of the cerebellum in dystonic tremor syndrome. Tremor phenotype may thus guide optimal intervention targets.

摘要

目的

确定小脑和运动皮层在张力障碍性震颤综合征中的因果作用,并探索锁相经颅交流电刺激(TACS)的治疗效果。

方法

我们在张力障碍性震颤综合征患者中应用同侧小脑(N=14)和对侧运动皮层(N=17)的锁相 TACS,同时患者保持诱发震颤的姿势。我们在每个目标的 10 个不同相位滞后(36 度增量)的 30 秒刺激期间使用加速度计测量震颤功率。事后,TACS 效应与一个关键的临床特征相关:震颤的急动性(规律性)。

结果

小脑 TACS 以相位依赖性方式调节震颤幅度,使得在相位周期的相反侧抑制或增强震颤幅度。这种效应仅在非急动性(正弦)震颤的患者(n=10)中存在,但在急动性(不规则)震颤的患者(n=4)中不存在。锁相刺激运动皮层不会调节震颤幅度。

结论

本研究表明小脑在(非急动性)张力障碍性震颤综合征的产生中起因果作用。我们的发现提示张力障碍性震颤综合征患者之间存在病理生理异质性,反映了临床变异性。

意义

我们显示了小脑在张力障碍性震颤综合征中的震颤表型依赖性参与。因此,震颤表型可能指导最佳干预靶点。

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