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Global network modulation during thalamic stimulation for Tourette syndromeopen access

Authors
Jo, Hang JoonMcCairn, Kevin W.Gibson, William S.Testini, PaolaZhao, Cong ZhiGorny, Krzysztof R.Felmlee, Joel P.Welker, Kirk M.Blaha, Charles D.Klassen, Bryan T.Min, Hoon-KiLee, Kendall H.
Issue Date
Feb-2018
Publisher
ELSEVIER SCI LTD
Keywords
Neurological disorders; Deep brain stimulation; Functional magnetic resonance imaging; Basal ganglia-cerebellar-thalamo-cortical networks; Vocal/motor tics
Citation
NEUROIMAGE-CLINICAL, v.18, pp.502 - 509
Indexed
SCIE
SCOPUS
Journal Title
NEUROIMAGE-CLINICAL
Volume
18
Start Page
502
End Page
509
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150536
DOI
10.1016/j.nicl.2018.02.018
ISSN
22131582
Abstract
Background and objectives: Deep brain stimulation (DBS) of the thalamus is a promising therapeutic alternative for treating medically refractory Tourette syndrome (TS). However, few human studies have examined its mechanism of action. Therefore, the networks that mediate the therapeutic effects of thalamic DBS remain poorly understood. Methods: Five participants diagnosed with severe medically refractory TS underwent bilateral thalamic DBS stereotactic surgery. Intraoperative fMRI characterized the blood oxygen level-dependent (BOLD) response evoked by thalamic DBS and determined whether the therapeutic effectiveness of thalamic DBS, as assessed using the Modified Rush Video Rating Scale test, would correlate with evoked BOLD responses in motor and limbic cortical and subcortical regions. Results: Our results reveal that thalamic stimulation in TS participants has wide-ranging effects that impact the frontostriatal, limbic, and motor networks. Thalamic stimulation induced suppression of motor and insula networks correlated with motor tic reduction, while suppression of frontal and parietal networks correlated with vocal tic reduction. These regions mapped closely to major regions of interest (ROI) identified in a nonhuman primate model of TS. Conclusions: Overall, these findings suggest that a critical factor in TS treatment should involve modulation of both frontostriatal and motor networks, rather than be treated as a focal disorder of the brain. Using the novel combination of DBS-evoked tic reduction and fMRI in human subjects, we provide new insights into the basal ganglia-cerebellar-thalamo-cortical network-level mechanisms that influence the effects of thalamic DBS. Future translational research should identify whether these network changes are cause or effect of TS symptoms.
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