Adaptive Brain Stimulation for Movement Disorders

Martijn Beudel, Hayriye Cagnan, Simon Little

    Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review

    13 Citations (Scopus)
    10 Downloads (Pure)

    Abstract

    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.

    Original languageEnglish
    Title of host publicationCurrent Concepts in Movement Disorder Management
    EditorsA. Niranjan, L.D. Lunsford, R.M. Richardson
    PublisherS. Karger AG
    Pages230-242
    Number of pages13
    Volume33
    ISBN (Electronic)978-3-318-06202-1
    ISBN (Print)978-3-318-06201-4
    DOIs
    Publication statusPublished - 2018

    Publication series

    NameProgress in Neurological Surgery
    ISSN (Print)0079-6492

    Fingerprint

    Dive into the research topics of 'Adaptive Brain Stimulation for Movement Disorders'. Together they form a unique fingerprint.

    Cite this