Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/2201
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dc.contributor.authorChen, Leo-
dc.contributor.authorHoy, Kate-
dc.contributor.authorFitzgerald, Paul-
dc.contributor.otherKaster, Tyler-
dc.contributor.otherBlumberger, Daniel-
dc.contributor.otherDaskalakis, Zafiris-
dc.date2020-02-
dc.date.accessioned2023-08-15T03:33:56Z-
dc.date.available2023-08-15T03:33:56Z-
dc.date.issued2020-05-
dc.identifier.citationBrain Stimul . 2020 May-Jun;13(3):850-857en_US
dc.identifier.issn1935-861Xen_US
dc.identifier.urihttp://hdl.handle.net/11434/2201-
dc.description.abstractBackground: To determine if an accelerated rTMS protocol results in distinct depressive symptom response trajectories, compared to a standard rTMS protocol. We also sought to validate previous analyses that identified distinct depressive symptom response trajectories with rTMS treatment using an external dataset. Method: Data from two recent clinical trials comparing accelerated rTMS protocol delivered to the left dorsolateral prefrontal cortex (DLPFC) with standard once-daily rTMS protocol were used to identify depressive symptom response trajectories. The accelerated protocol in Trial 1 was conventional 10-Hz rTMS, while Trial 2 employed intermittent theta burst stimulation (iTBS). Participants were adult outpatients (18-70 years old) with bipolar or unipolar depression and moderate-severe depression (Montgomery Asberg Depression Rating Scale score >19) who had failed to respond to adequate courses of two different antidepressants. We used group-based trajectory modeling to identify MADRS response trajectories, and regression techniques adjusting for baseline depressive symptom severity to determine the association between treatment protocol and depressive symptom response trajectory. Results: Treatment outcomes of 189 participants were analysed. We identified four distinct response trajectories: "nonresponse" (N = 59; 30.7%), "minimal response" (N = 65; 34.1%), "higher symptoms, response" (N = 26; 14.6%), "lower symptoms, response" (N = 39; 20.6%). We failed to find an association between rTMS protocol (accelerated vs standard) with depressive symptom response trajectory even after adjusting for baseline depressive symptom severity. Conclusion: The accelerated rTMS protocol in this study did not impact depressive symptom response trajectories. This work provides further confirmatory evidence that there are distinct depressive symptom response trajectories with rTMS delivered to the left DLPFC.en_US
dc.publisherElsevieren_US
dc.subjectRepetitive Transcranial Magnetic Stimulationen_US
dc.subjectrTMSen_US
dc.subjectBipolar Affective Disorderen_US
dc.subjectMajor Depressive Disorderen_US
dc.subjectLeft Dorsolateral Prefrontal Cortexen_US
dc.subjectDLPFCen_US
dc.subjectAccelerated rTMSen_US
dc.subjectStandard rTMSen_US
dc.subjectMontgomery Asberg Depression Rating Scaleen_US
dc.subjectGroup-Based Trajectory Modelingen_US
dc.subjectRehabilitation, Mental Health and Chronic Pain Clinical Institute, Epworth HealthCare, Victoria, Australia.en_US
dc.subjectNeurosciences Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.titleDepressive symptom trajectories associated with standard and accelerated rTMS.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.brs.2020.02.021en_US
dc.identifier.journaltitleBrain Stimulationen_US
dc.description.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/32289716/en_US
dc.description.affiliatesTemerty Centre for Therapeutic Brain Intervention, Centre for Addiction and Mental Health, Toronto, Canadaen_US
dc.description.affiliatesDepartment of Psychiatry, University of Toronto, Toronto, Canadaen_US
dc.description.affiliatesCampbell Family Mental Health Research Institute Centre for Addiction and Mental Health, Toronto, Canadaen_US
dc.description.affiliatesMonash University Central Clinical School, Camberwell, Victoria, Australiaen_US
dc.type.studyortrialComparative Studyen_US
dc.type.contenttypeTexten_US
Appears in Collections:Neurosciences

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