Beudel Martijn, Cagnan Hayriye, Little Simon
Prog Neurol Surg. 2018;33:230-242. doi: 10.1159/000481107. Epub 2018 Jan 12.
Deep brain stimulation (DBS) has markedly changed how we treat movement disorders including Parkinson's disease (PD), dystonia, and essential tremor (ET). However, despite its demonstrable clinical benefit, DBS is often limited by side effects and partial efficacy. These limitations may be due in part to the fact that DBS interferes with both pathological and physiological neural activities. DBS could, therefore, be potentially improved were it applied selectively and only at times of enhanced pathological activity. This form of stimulation is known as closed-loop or adaptive DBS (aDBS). An aDBS approach has been shown to be superior to conventional DBS in PD in primates using cortical neuronal spike triggering and in humans employing local field potential biomarkers. Likewise, aDBS studies for essential and Parkinsonian tremor are advancing and show great promise, using both peripheral or central sensing and stimulation. aDBS has not yet been trialed in dystonia and yet exciting and promising biomarkers suggest it could be beneficial here too. In this chapter, we will review the existing literature on aDBS in movement disorders and explore potential biomarkers and stimulation algorithms for applying aDBS in PD, ET, and dystonia.
深部脑刺激(DBS)显著改变了我们治疗包括帕金森病(PD)、肌张力障碍和特发性震颤(ET)在内的运动障碍的方式。然而,尽管DBS具有明显的临床益处,但它常常受到副作用和部分疗效的限制。这些限制可能部分归因于DBS会干扰病理性和生理性神经活动这一事实。因此,如果DBS能够选择性地且仅在病理性活动增强时应用,那么它可能会得到潜在的改善。这种刺激形式被称为闭环或适应性DBS(aDBS)。在灵长类动物中,使用皮层神经元尖峰触发的aDBS方法已被证明在帕金森病中优于传统DBS;在人类中,采用局部场电位生物标志物的aDBS方法也有类似效果。同样,针对特发性震颤和帕金森震颤的aDBS研究也在推进,并显示出巨大的前景,这些研究同时使用外周或中枢传感与刺激。aDBS尚未在肌张力障碍中进行试验,但令人兴奋且有前景的生物标志物表明它在这里也可能有益。在本章中,我们将回顾关于aDBS在运动障碍方面的现有文献,并探索将aDBS应用于帕金森病、特发性震颤和肌张力障碍的潜在生物标志物和刺激算法。