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dc.contributor.authorZhuo, Kaiming
dc.contributor.authorTang, Yingying
dc.contributor.authorSong, Zhenhua
dc.contributor.authorWang, Yingchan
dc.contributor.authorWang, Junjie
dc.contributor.authorQian, Zhenying
dc.contributor.authorLi, Hui
dc.contributor.authorXiang, Qiong
dc.contributor.authorChen, Tianyi
dc.contributor.authorYang, Zhilei
dc.contributor.authorXu, Yifeng
dc.contributor.authorFan, Xiaoduo
dc.contributor.authorWang, Jijun
dc.contributor.authorLiu, Dengtang
dc.date2022-08-11T08:09:53.000
dc.date.accessioned2022-08-23T16:47:24Z
dc.date.available2022-08-23T16:47:24Z
dc.date.issued2019-05-08
dc.date.submitted2019-07-08
dc.identifier.citation<p>Neuropsychiatr Dis Treat. 2019 May 8;15:1141-1150. doi: 10.2147/NDT.S196086. eCollection 2019. <a href="https://doi.org/10.2147/NDT.S196086">Link to article on publisher's site</a></p>
dc.identifier.issn1176-6328 (Linking)
dc.identifier.doi10.2147/NDT.S196086
dc.identifier.pmid31190822
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41070
dc.description.abstractPurpose: Effective treatment options for negative symptoms and cognitive impairment in patients with schizophrenia are still to be developed. The present study was to examine potential benefits of repetitive transcranial magnetic stimulation (rTMS) to improve negative symptoms and cognition in this patient population. Methods: The study was a 4-week, randomized, double-blind sham-controlled trial. Patients with schizophrenia were treated with adjunctive 20-Hz rTMS for 4 weeks or sham condition to the left dorsolateral prefrontal cortex (DLPFC). Negative symptoms were measured using the Scale for the Assessment of Negative Symptoms (SANS) and the Positive and Negative symptom scale (PANSS) negative subscale at baseline and week 4. Cognitive function was measured using the MATRICS Consensus Cognitive Battery (MCCB) at the same two time points. In addition, possible moderators for rTMS treatment efficacy were explored. Results: Sixty patients (33 in the treatment group, 27 in the sham group) completed the study. There was a significant decrease in negative symptoms after 4-week rTMS treatment as measured by the SANS total score and the PANSS negative symptom subscale score. However, there was no significant improvement in cognition with rTMS treatment. Stepwise multiple linear regression analysis suggested that the baseline severity of positive symptoms may predict poorer improvement in negative symptoms at week 4. Conclusion: Twenty-Hz rTMS stimulation over left DLPFC as an adjunctive treatment might be beneficial in improving negative symptoms of schizophrenia. Future studies with a longer treatment duration and a larger sample size are needed. Clinical trial ID: NCT01940939.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=31190822&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rights© 2019 Zhuo et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/
dc.subjectMCCB
dc.subjectcognitive impairment
dc.subjectnegative symptoms
dc.subjectrepetitive transcranial magnetic stimulation
dc.subjectrTMS
dc.subjectschizophrenia
dc.subjectHealth Services Administration
dc.subjectHealth Services Research
dc.subjectMental Disorders
dc.subjectNervous System
dc.subjectPsychiatry
dc.subjectTherapeutics
dc.titleRepetitive transcranial magnetic stimulation as an adjunctive treatment for negative symptoms and cognitive impairment in patients with schizophrenia: a randomized, double-blind, sham-controlled trial
dc.typeJournal Article
dc.source.journaltitleNeuropsychiatric disease and treatment
dc.source.volume15
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4875&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3860
dc.identifier.contextkey14880264
refterms.dateFOA2022-08-23T16:47:24Z
html.description.abstract<p>Purpose: Effective treatment options for negative symptoms and cognitive impairment in patients with schizophrenia are still to be developed. The present study was to examine potential benefits of repetitive transcranial magnetic stimulation (rTMS) to improve negative symptoms and cognition in this patient population.</p> <p>Methods: The study was a 4-week, randomized, double-blind sham-controlled trial. Patients with schizophrenia were treated with adjunctive 20-Hz rTMS for 4 weeks or sham condition to the left dorsolateral prefrontal cortex (DLPFC). Negative symptoms were measured using the Scale for the Assessment of Negative Symptoms (SANS) and the Positive and Negative symptom scale (PANSS) negative subscale at baseline and week 4. Cognitive function was measured using the MATRICS Consensus Cognitive Battery (MCCB) at the same two time points. In addition, possible moderators for rTMS treatment efficacy were explored.</p> <p>Results: Sixty patients (33 in the treatment group, 27 in the sham group) completed the study. There was a significant decrease in negative symptoms after 4-week rTMS treatment as measured by the SANS total score and the PANSS negative symptom subscale score. However, there was no significant improvement in cognition with rTMS treatment. Stepwise multiple linear regression analysis suggested that the baseline severity of positive symptoms may predict poorer improvement in negative symptoms at week 4.</p> <p>Conclusion: Twenty-Hz rTMS stimulation over left DLPFC as an adjunctive treatment might be beneficial in improving negative symptoms of schizophrenia. Future studies with a longer treatment duration and a larger sample size are needed.</p> <p>Clinical trial ID: NCT01940939.</p>
dc.identifier.submissionpathoapubs/3860
dc.contributor.departmentDepartment of Psychiatry
dc.contributor.departmentPsychotic Disorders Program, UMass Memorial Medical Center
dc.source.pages1141-1150


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© 2019 Zhuo et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php
and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
Except where otherwise noted, this item's license is described as © 2019 Zhuo et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).