4.8 Article

Non-invasive suppression of essential tremor via phase-locked disruption of its temporal coherence

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-020-20581-7

Keywords

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Funding

  1. Swiss National Science Foundation
  2. Swiss Neurological Society
  3. European Academy of Neurology
  4. EMDO Foundation fellowship
  5. CT Institute
  6. US NSF CAREER Award [1845348]
  7. Wellcome Trust MRC strategic neurodegenerative disease initiative award
  8. Dystonia Coalition
  9. Parkinson's UK [G-1009]
  10. EPSRC [EP/N014529/1]
  11. NIH [R01MH117063]
  12. HHMI
  13. DARPA [D20AC00004]
  14. UK Dementia Research Institute (UK DRI)-an initiative - Medical Research Council
  15. Alzheimer's Society
  16. Alzheimer's Research UK
  17. Wellcome Trust fellowship [097443/Z/ 11/Z]
  18. Science & PINS Award for Neuromodulation
  19. NIHR IBRC Confident in Concept Award
  20. [WT089698]
  21. MRC [UKDRI-5005] Funding Source: UKRI
  22. Wellcome Trust [097443/Z/11/Z] Funding Source: Wellcome Trust
  23. Directorate For Engineering
  24. Div Of Electrical, Commun & Cyber Sys [1845348] Funding Source: National Science Foundation

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The study introduces a new method for real-time tracking of neural oscillations, which can be used to suppress aberrant neural oscillations associated with specific disorders, offering a new approach for the treatment of brain disorders.
Aberrant neural oscillations hallmark numerous brain disorders. Here, we first report a method to track the phase of neural oscillations in real-time via endpoint-corrected Hilbert transform (ecHT) that mitigates the characteristic Gibbs distortion. We then used ecHT to show that the aberrant neural oscillation that hallmarks essential tremor (ET) syndrome, the most common adult movement disorder, can be transiently suppressed via transcranial electrical stimulation of the cerebellum phase-locked to the tremor. The tremor suppression is sustained shortly after the end of the stimulation and can be phenomenologically predicted. Finally, we use feature-based statistical-learning and neurophysiological-modelling to show that the suppression of ET is mechanistically attributed to a disruption of the temporal coherence of the aberrant oscillations in the olivocerebellar loop, thus establishing its causal role. The suppression of aberrant neural oscillation via phase-locked driven disruption of temporal coherence may in the future represent a powerful neuromodulatory strategy to treat brain disorders. Aberrant synchronous oscillations have been associated with numerous brain disorders, including essential tremor. The authors show that synchronous cerebellar activity can casually affect essential tremor and that its underlying mechanism may be related to the temporal coherence of the tremulous movement.

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