1 Department of Neurology, University Hospital Schleswig-Holstein, Campus Kiel, D-24105, Germany.
Brain. 2014 Jan;137(Pt 1):109-21. doi: 10.1093/brain/awt304. Epub 2013 Nov 25.
Postural tremor is the leading symptom in essential tremor, but in some cases intention tremor and limb ataxia emerge and can become highly disabling features. Deep brain stimulation of the thalamus or subthalamic white matter improve tremor and ataxia; however, the underlying network mechanisms are enigmatic. To elucidate the mechanisms of deep brain stimulation in essential tremor, we pursued a multimodal approach combining kinematic measures of reach-to-grasp movements, clinical assessments, physiological measures of neuronal excitability and probabilistic tractography from diffusion tensor imaging. Seven patients with essential tremor (age 62.9 ± 10.3 years, two females) received thalamic deep brain stimulation and a clinical examination of severity of limb tremor and ataxia at off stimulation, using therapeutic and supratherapeutic stimulation parameters. A reach-to-grasp task based on acoustic cues was also performed. To examine the electrical properties of target structures, we determined the chronaxie of neural elements modulated. A control group of 13 healthy subjects (age 56 ± 7.6 years, five females) underwent whole-brain diffusion tensor imaging at 3 T. Probabilistic tractography was applied in healthy subjects from seeds in cerebellum and midbrain to reconstruct the connectivity pattern of the subthalamic area. The positions of stimulation electrodes in patients were transferred into probability maps and connectivity values were correlated to clinical outcome measures. Therapeutic stimulation improved ataxia and tremor mainly during the target period of the reaching paradigm (63% reduction compared with off stimulation). Notably the acceleration (29%) and deceleration periods (41%) were improved. By contrast, supratherapeutic stimulation worsened ataxia during the deceleration period with a 55% increase of spatial variability, while maintaining near complete suppression of tremor. Chronaxie measures were in the range of rapidly-conducting myelinated fibres with significantly different values for the anti-tremor effect of therapeutic stimulation (27 s) and the pro-ataxic effect of supratherapeutic stimulation (52 s). The degree of connectivity to the dentato-thalamic tract at the stimulating electrode correlated significantly with the reduction of tremor in the therapeutic condition. Our data suggest that stimulation induced tremor reduction and induction of ataxia by supratherapeutic stimulation are mediated by different fibre systems. Probalistic tractography identified the dentato-thalamic tract as a likely target of tremor suppression. Stimulation-induced ataxia may be caused by additional recruitment of adjacent fibre systems at higher amplitudes. Stimulation with short pulse duration may help to increase the therapeutic window and focus on the anti-tremor effect.
姿势性震颤是原发性震颤的主要症状,但在某些情况下,意向性震颤和肢体共济失调会出现,并可能成为高度致残的特征。丘脑或底丘脑白质的深部脑刺激可改善震颤和共济失调;然而,其潜在的网络机制尚不清楚。为了阐明原发性震颤深部脑刺激的机制,我们采用了一种多模态方法,结合了到达抓握运动的运动学测量、临床评估、神经元兴奋性的生理测量以及来自扩散张量成像的概率轨迹追踪。七名原发性震颤患者(年龄 62.9 ± 10.3 岁,女性 2 名)接受了丘脑深部脑刺激,并在治疗和超治疗刺激参数下进行了肢体震颤和共济失调严重程度的临床检查。还进行了基于声学提示的到达抓握任务。为了检查目标结构的电特性,我们确定了调制的神经元件的驰豫时间。一组 13 名健康受试者(年龄 56 ± 7.6 岁,女性 5 名)在 3T 下进行了全脑扩散张量成像。将患者刺激电极的位置转移到概率图中,并将连通值与临床结果测量相关联。治疗性刺激主要在到达范式的目标期改善了共济失调和震颤(与关闭刺激相比减少了 63%)。值得注意的是,加速度(29%)和减速期(41%)得到了改善。相比之下,超治疗性刺激在减速期使共济失调恶化,空间变异性增加了 55%,同时保持了震颤的几乎完全抑制。驰豫时间测量值处于快速传导的有髓纤维范围内,治疗性刺激的抗震颤效应(27s)和超治疗性刺激的促共济失调效应(52s)的数值有显著差异。刺激电极处与齿状丘脑束的连通程度与治疗条件下震颤减少显著相关。我们的数据表明,刺激引起的震颤减轻和超治疗性刺激引起的共济失调诱导是由不同的纤维系统介导的。概率轨迹追踪确定齿状丘脑束是震颤抑制的可能靶点。刺激引起的共济失调可能是由于在更高振幅下额外募集相邻的纤维系统引起的。使用短脉冲持续时间的刺激可能有助于增加治疗窗口并专注于抗震颤效应。