Randomized Sham Controlled Double-blind Trial of Repetitive Transcranial Magnetic Stimulation for Adults With Severe Tourette Syndrome
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | LANDEROS-WEISENBERGER, Angeli | |
dc.contributor.author | MANTOVANI, Antonio | |
dc.contributor.author | MOTLAGH, Maria G. | |
dc.contributor.author | ALVARENGA, Pedro Gomes de | |
dc.contributor.author | KATSOVICH, Liliya | |
dc.contributor.author | LECKMAN, James F. | |
dc.contributor.author | LISANBY, Sarah H. | |
dc.date.accessioned | 2015-10-26T16:33:34Z | |
dc.date.available | 2015-10-26T16:33:34Z | |
dc.date.issued | 2015 | |
dc.description.abstract | Background: A small proportion of individuals with Tourette syndrome (TS) have a lifelong course of illness that fails to respond to conventional treatments. Open label studies have suggested that low frequency (1-Hz) repetitive transcranial magnetic stimulation (rTMS) targeting the supplementary motor area (SMA) may be effective in reducing tic severity. Objective/Hypothesis: To examine the efficacy of rTMS over the SMA for TS in a randomized double-blind sham-controlled trial (RCT). Methods: We conducted a two-site RCT-rTMS with 20 adults with severe TS for 3 weeks. Treatment consisted of 15 sessions (1-Hz; 30 min; 1800 pulses per day) of active or sham rTMS at 110% of the motor threshold over the SMA. A subsequent 3 week course of active rTMS treatment was offered. Results: Of the 20 patients (16 males; mean age of 33.7 + 12.2 years), 9 received active and 11 received sham rTMS. After 3 weeks, patients receiving active rTMS showed on average a 17.3% reduction in the YGTSS total tic score compared to a 13.2% reduction in those receiving sham rTMS, resulting in no statistically significant reduction in tic severity (P = 0.27). An additional 3 week open label active treatment for those patients (n = 7) initially randomized to active rTMS resulted in a significant overall 29.7% reduction in tic severity compared to baseline (P = 0.04). Conclusion: This RCT did not demonstrate efficacy of 3-week SMA-targeted low frequency rTMS in the treatment of severe adult TS. Further studies using longer or alternative stimulation protocols are warranted. | |
dc.description.index | MEDLINE | |
dc.description.sponsorship | Tourette Syndrome Association | |
dc.description.sponsorship | National Institute of Mental Health [R21MH082323 [NCT00529308]] | |
dc.description.sponsorship | Echlin Foundation | |
dc.description.sponsorship | Rembrandt Foundation | |
dc.identifier.citation | BRAIN STIMULATION, v.8, n.3, p.574-581, 2015 | |
dc.identifier.doi | 10.1016/j.brs.2014.11.015 | |
dc.identifier.eissn | 1876-4754 | |
dc.identifier.issn | 1935-861X | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/11859 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER SCIENCE INC | |
dc.relation.ispartof | Brain Stimulation | |
dc.rights | restrictedAccess | |
dc.rights.holder | Copyright ELSEVIER SCIENCE INC | |
dc.subject | Tourette syndrome | |
dc.subject | Transcranial | |
dc.subject | Magnetic stimulation | |
dc.subject | Randomized controlled trial | |
dc.subject.other | obsessive-compulsive disorder | |
dc.subject.other | supplementary motor area | |
dc.subject.other | 1 hz rtms | |
dc.subject.other | european clinical guidelines | |
dc.subject.other | cerebral-blood-flow | |
dc.subject.other | tic disorders | |
dc.subject.other | functional mri | |
dc.subject.other | scale | |
dc.subject.other | inhibition | |
dc.subject.other | cortex | |
dc.subject.wos | Clinical Neurology | |
dc.subject.wos | Neurosciences | |
dc.title | Randomized Sham Controlled Double-blind Trial of Repetitive Transcranial Magnetic Stimulation for Adults With Severe Tourette Syndrome | |
dc.type | article | |
dc.type.category | original article | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.affiliation.country | Estados Unidos | |
hcfmusp.affiliation.countryiso | us | |
hcfmusp.author.external | LANDEROS-WEISENBERGER, Angeli:Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06520 USA | |
hcfmusp.author.external | MANTOVANI, Antonio:CUNY, Sophie Davis Sch Biomed Educ, Dept Physiol Pharmacol & Neurosci, New York, NY USA; Columbia Univ, New York State Psychiat Inst, Dept Psychiat, Div Expt Therapeut, New York, NY USA | |
hcfmusp.author.external | MOTLAGH, Maria G.:Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06520 USA; Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06520 USA | |
hcfmusp.author.external | KATSOVICH, Liliya:Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06520 USA | |
hcfmusp.author.external | LECKMAN, James F.:Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06520 USA | |
hcfmusp.author.external | LISANBY, Sarah H.:Duke Univ, Dept Psychiat & Behav Sci, Durham, NC USA | |
hcfmusp.citation.scopus | 61 | |
hcfmusp.contributor.author-fmusphc | PEDRO GOMES DE ALVARENGA | |
hcfmusp.description.beginpage | 574 | |
hcfmusp.description.endpage | 581 | |
hcfmusp.description.issue | 3 | |
hcfmusp.description.volume | 8 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 25912296 | |
hcfmusp.origem.scopus | 2-s2.0-84941599216 | |
hcfmusp.origem.wos | WOS:000355772300019 | |
hcfmusp.publisher.city | NEW YORK | |
hcfmusp.publisher.country | USA | |
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