Literature DB >> 32139653

Differentiating tic electrophysiology from voluntary movement in the human thalamocortical circuit.

Jackson N Cagle1, Michael S Okun2, Enrico Opri1, Stephanie Cernera1, Rene Molina3, Kelly D Foote4, Aysegul Gunduz5.   

Abstract

OBJECTIVES: Tourette syndrome is a neurodevelopmental disorder commonly associated with involuntary movements, or tics. We currently lack an ideal animal model for Tourette syndrome. In humans, clinical manifestation of tics cannot be captured via functional imaging due to motion artefacts and limited temporal resolution, and electrophysiological studies have been limited to the intraoperative environment. The goal of this study was to identify electrophysiological signals in the centromedian (CM) thalamic nucleus and primary motor (M1) cortex that differentiate tics from voluntary movements.
METHODS: The data were collected as part of a larger National Institutes of Health-sponsored clinical trial. Four participants (two males, two females) underwent monthly clinical visits for collection of physiology for a total of 6 months. Participants were implanted with bilateral CM thalamic macroelectrodes and M1 subdural electrodes that were connected to two neurostimulators, both with sensing capabilities. MRI scans were performed preoperatively and CT scans postoperatively for localisation of electrodes. Electrophysiological recordings were collected at each visit from both the cortical and subcortical implants.
RESULTS: Recordings collected from the CM thalamic nucleus revealed a low-frequency power (3-10 Hz) increase that was time-locked to the onset of involuntary tics but was not present during voluntary movements. Cortical recordings revealed beta power decrease in M1 that was present during tics and voluntary movements.
CONCLUSION: We conclude that a human physiological signal was detected from the CM thalamus that differentiated tic from voluntary movement, and this physiological feature could potentially guide the development of neuromodulation therapies for Tourette syndrome that could use a closed-loop-based approach. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Year:  2020        PMID: 32139653      PMCID: PMC7296862          DOI: 10.1136/jnnp-2019-321973

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  35 in total

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7.  Pallidal and thalamic neural oscillatory patterns in tourette's syndrome.

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Authors:  Lauren E Schrock; Jonathan W Mink; Douglas W Woods; Mauro Porta; Dominico Servello; Veerle Visser-Vandewalle; Peter A Silburn; Thomas Foltynie; Harrison C Walker; Joohi Shahed-Jimenez; Rodolfo Savica; Bryan T Klassen; Andre G Machado; Kelly D Foote; Jian-Guo Zhang; Wei Hu; Linda Ackermans; Yasin Temel; Zoltan Mari; Barbara K Changizi; Andres Lozano; M Auyeung; Takanobu Kaido; Yves Agid; Marie L Welter; Suketu M Khandhar; Alon Y Mogilner; Michael H Pourfar; Benjamin L Walter; Jorge L Juncos; Robert E Gross; Jens Kuhn; James F Leckman; Joseph A Neimat; Michael S Okun
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9.  Controlled study of haloperidol, pimozide and placebo for the treatment of Gilles de la Tourette's syndrome.

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10.  Beta oscillations in freely moving Parkinson's subjects are attenuated during deep brain stimulation.

Authors:  Emma J Quinn; Zack Blumenfeld; Anca Velisar; Mandy Miller Koop; Lauren A Shreve; Megan H Trager; Bruce C Hill; Camilla Kilbane; Jaimie M Henderson; Helen Brontë-Stewart
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Journal:  Brain       Date:  2020-08-01       Impact factor: 13.501

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  2 in total

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