Cortico-thalamic tremor circuits and their associations with deep brain stimulation effects in essential tremor

IF 10.6 1区 医学 Q1 CLINICAL NEUROLOGY Brain Pub Date : 2024-11-27 DOI:10.1093/brain/awae387
Shenghong He, Timothy O West, Fernando R Plazas, Laura Wehmeyer, Alek Pogosyan, Alceste Deli, Christoph Wiest, Damian M Herz, Thomas Simpson, Pablo Andrade, Fahd Baig, Michael G Hart, Francesca Morgante, James J FitzGerald, Michael T Barbe, Veerle Visser-Vandewalle, Alexander L Green, Erlick A Pereira, Hayriye Cagnan, Huiling Tan
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Abstract

Essential tremor (ET) is one of the most common movement disorders in adults. Deep brain stimulation (DBS) of the ventralis intermediate nucleus (VIM) of the thalamus and/or the posterior subthalamic area (PSA) has been shown to provide significant tremor suppression in patients with ET, but with significant inter-patient variability and habituation to the stimulation. Several non-invasive neuromodulation techniques targeting other parts of the central nervous system, including cerebellar, motor cortex, or peripheral nerves, have also been developed for treating ET, but the clinical outcomes remain inconsistent. Existing studies suggest that pathology in ET may emerge from multiple cortical and subcortical areas, but its exact mechanisms remain unclear. By simultaneously capturing neural activities from motor cortices and thalami, and hand tremor signals recorded via accelerometers in fifteen human subjects who have undergone lead implantations for DBS, we systematically characterized the efferent and afferent cortico-thalamic tremor networks. Through the comparisons of these network characteristics and tremor amplitude between DBS OFF and ON conditions, we further investigated the associations between different tremor network characteristics and the magnitude of DBS effect. Our findings implicate the thalamus, specifically the contralateral hemisphere, as the primary generator of tremor in ET, with a significant contribution of the ipsilateral hemisphere as well. Although there is no direct correlation between the cortico-tremor connectivity and tremor power or reduced tremor by DBS, the strength of connectivity from the motor cortex to the thalamus and vice versa at tremor frequency predicts baseline tremor power and effect of DBS. Interestingly, there is no correlation between these two connectivity pathways themselves, suggesting that, independent of the subcortical pathway, the motor cortex appears to play a relatively distinct role, possibly mediated through an afferent/feedback loop in the propagation of tremor. DBS has a greater clinical effect in those with stronger cortico-thalamo-tremor connectivity involving the contralateral thalamus, which is also associated with bigger and more stable tremor measured with an accelerometer. Interestingly, stronger cross-hemisphere coupling between left and right thalami is associated with more unstable tremor. Together this study provides important insights into a better understanding of the cortico-thalamic tremor generating network and its implication for the development of patient-specific therapeutic approaches for ET.
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皮质-丘脑震颤回路及其与深度脑刺激对本质性震颤影响的关系
本质性震颤(ET)是成人中最常见的运动障碍之一。对丘脑腹侧中间核(VIM)和/或眼下丘脑后区(PSA)的深部脑刺激(DBS)已被证明能显著抑制 ET 患者的震颤,但患者之间的差异很大,对刺激也会产生习惯性反应。针对中枢神经系统其他部位(包括小脑、运动皮层或周围神经)的一些非侵入性神经调控技术也已开发出来用于治疗 ET,但临床效果仍不一致。现有研究表明,ET 的病理变化可能来自多个皮层和皮层下区域,但其确切机制仍不清楚。通过同时捕捉 15 名接受过 DBS 导联植入术的受试者运动皮层和丘脑的神经活动以及通过加速度计记录的手部震颤信号,我们系统地描述了传出和传入皮层-丘脑震颤网络的特征。通过比较这些网络特征和 DBS 关闭与开启条件下的震颤幅度,我们进一步研究了不同震颤网络特征与 DBS 效果大小之间的关联。我们的研究结果表明,丘脑,特别是对侧半球,是 ET 震颤的主要发生器,同侧半球也有重要贡献。虽然皮质-震颤连通性与震颤力或通过 DBS 减轻震颤之间没有直接的相关性,但在震颤频率下,运动皮质与丘脑之间以及丘脑与运动皮质之间的连通性强度可预测基线震颤力和 DBS 的效果。有趣的是,这两种连接途径本身之间并不存在相关性,这表明运动皮层似乎在震颤的传播中扮演着相对独特的角色,可能是通过传入/反馈回路介导的,而与皮层下途径无关。DBS 对涉及对侧丘脑的皮质-丘脑-震颤连通性更强的患者有更大的临床效果,这也与用加速度计测量的震颤更大、更稳定有关。有趣的是,左右丘脑之间更强的跨半球耦合与更不稳定的震颤有关。这项研究为更好地了解皮质丘脑震颤生成网络及其对开发针对特定患者的 ET 治疗方法的意义提供了重要见解。
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来源期刊
Brain
Brain 医学-临床神经学
CiteScore
20.30
自引率
4.10%
发文量
458
审稿时长
3-6 weeks
期刊介绍: Brain, a journal focused on clinical neurology and translational neuroscience, has been publishing landmark papers since 1878. The journal aims to expand its scope by including studies that shed light on disease mechanisms and conducting innovative clinical trials for brain disorders. With a wide range of topics covered, the Editorial Board represents the international readership and diverse coverage of the journal. Accepted articles are promptly posted online, typically within a few weeks of acceptance. As of 2022, Brain holds an impressive impact factor of 14.5, according to the Journal Citation Reports.
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