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dc.contributor.authorO’Brien, Anthony T.
dc.contributor.authorAmorim, Rivadavio
dc.contributor.authorRushmore, R. Jarrett
dc.contributor.authorEden, Uri
dc.contributor.authorAfifi, Linda
dc.contributor.authorDipietro, Laura
dc.contributor.authorValero-Cabré, Antoni
dc.contributor.authorWagner, Tim Andrew
dc.date.accessioned2017-02-21T15:45:38Z
dc.date.available2017-02-21T15:45:38Z
dc.date.issued2016-11
dc.date.submitted2016-10
dc.identifier.issn1662-5161
dc.identifier.urihttp://hdl.handle.net/1721.1/107000
dc.description.abstractBackground: Central post stroke pain (CPSP) is a highly refractory syndrome that can occur after stroke. Primary motor cortex (M1) brain stimulation using epidural brain stimulation (EBS), transcranial magnetic stimulation (TMS), and transcranial direct current stimulation (tDCS) have been explored as potential therapies for CPSP. These techniques have demonstrated variable clinical efficacy. It is hypothesized that changes in the stimulating currents that are caused by stroke-induced changes in brain tissue conductivity limit the efficacy of these techniques. Methods: We generated MRI-guided finite element models of the current density distributions in the human head and brain with and without chronic focal cortical infarctions during EBS, TMS, and tDCS. We studied the change in the stimulating current density distributions’ magnitude, orientation, and maxima locations between the different models. Results: Changes in electrical properties at stroke boundaries altered the distribution of stimulation currents in magnitude, location, and orientation. Current density magnitude alterations were larger for the non-invasive techniques (i.e., tDCS and TMS) than for EBS. Nonetheless, the lesion also altered currents during EBS. The spatial shift of peak current density, relative to the size of the stimulation source, was largest for EBS. Conclusion: In order to maximize therapeutic efficiency, neurostimulation trials need to account for the impact of anatomically disrupted neural tissues on the location, orientation, and magnitude of exogenously applied currents. The relative current-neuronal structure should be considered when planning stimulation treatment, especially across techniques (e.g., using TMS to predict EBS response). We postulate that the effects of altered tissue properties in stroke regions may impact stimulation induced analgesic effects and/or lead to highly variable outcomes during brain stimulation treatments in CPSP.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grants (R01-NS33975, R21-NS062317, R21-NS084022, R44-AT008637, and R44NS080632)en_US
dc.description.sponsorshipNational Institute of Neurological Disorders and Stroke (U.S.) (Award R44NS080632)en_US
dc.description.sponsorshipNational Center for Complementary and Integrative Health (U.S.)en_US
dc.language.isoen_US
dc.publisherFrontiers Research Foundationen_US
dc.relation.isversionofhttp://dx.doi.org/10.3389/fnhum.2016.00545en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceFrontiersen_US
dc.titleMotor Cortex Neurostimulation Technologies for Chronic Post-stroke Pain: Implications of Tissue Damage on Stimulation Currentsen_US
dc.typeArticleen_US
dc.identifier.citationO’Brien, Anthony T. et al. “Motor Cortex Neurostimulation Technologies for Chronic Post-Stroke Pain: Implications of Tissue Damage on Stimulation Currents.” Frontiers in Human Neuroscience 10 (2016): n. pag.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorWagner, Tim Andrew
dc.relation.journalFrontiers in Human Neuroscienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsO’Brien, Anthony T.; Amorim, Rivadavio; Rushmore, R. Jarrett; Eden, Uri; Afifi, Linda; Dipietro, Laura; Wagner, Timothy; Valero-Cabré, Antonien_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5835-4256
mit.licensePUBLISHER_CCen_US


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