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A multivariate neuroimaging biomarker of individual outcome to transcranial magnetic stimulation in depression.
Cash, Robin F H; Cocchi, Luca; Anderson, Rodney; Rogachov, Anton; Kucyi, Aaron; Barnett, Alexander J; Zalesky, Andrew; Fitzgerald, Paul B.
Afiliación
  • Cash RFH; Monash Alfred Psychiatry Research Centre, Melbourne, Australia.
  • Cocchi L; Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.
  • Anderson R; Department of Biomedical Engineering, The University of Melbourne, Melbourne, Victoria, Australia.
  • Rogachov A; Clinical Brain Networks Group, QIMR Berghofer, Brisbane, Australia.
  • Kucyi A; Monash Alfred Psychiatry Research Centre, Melbourne, Australia.
  • Barnett AJ; Division of Brain, Imaging, and Behaviour - Systems Neuroscience, Krembil Research Institute, Toronto Western Hospital, Toronto, Ontario, Canada.
  • Zalesky A; Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada.
  • Fitzgerald PB; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California.
Hum Brain Mapp ; 40(16): 4618-4629, 2019 11 01.
Article en En | MEDLINE | ID: mdl-31332903
ABSTRACT
The neurobiology of major depressive disorder (MDD) remains incompletely understood, and many individuals fail to respond to standard treatments. Repetitive transcranial magnetic stimulation (rTMS) of the dorsolateral prefrontal cortex (DLPFC) has emerged as a promising antidepressant therapy. However, the heterogeneity of response underscores a pressing need for biomarkers of treatment outcome. We acquired resting state functional magnetic resonance imaging (rsfMRI) data in 47 MDD individuals prior to 5-8 weeks of rTMS treatment targeted using the F3 beam approach and in 29 healthy comparison subjects. The caudate, prefrontal cortex, and thalamus showed significantly lower blood oxygenation level-dependent (BOLD) signal power in MDD individuals at baseline. Critically, individuals who responded best to treatment were associated with lower pre-treatment BOLD power in these regions. Additionally, functional connectivity (FC) in the default mode and affective networks was associated with treatment response. We leveraged these findings to train support vector machines (SVMs) to predict individual treatment responses, based on learned patterns of baseline FC, BOLD signal power and clinical features. Treatment response (responder vs. nonresponder) was predicted with 85-95% accuracy. Reduction in symptoms was predicted to within a mean error of ±16% (r = .68, p < .001). These preliminary findings suggest that therapeutic outcome to DLPFC-rTMS could be predicted at a clinically meaningful level using only a small number of core neurobiological features of MDD, warranting prospective testing to ascertain generalizability. This provides a novel, transparent and physiologically plausible multivariate approach for classification of individual response to what has become the most commonly employed rTMS treatment worldwide. This study utilizes data from a larger clinical study (Australian New Zealand Clinical Trials Registry Investigating Predictors of Response to Transcranial Magnetic Stimulation for the Treatment of Depression; ACTRN12610001071011; https//www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=336262).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor / Estimulación Magnética Transcraneal / Neuroimagen Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Brain Mapp Asunto de la revista: CEREBRO Año: 2019 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor / Estimulación Magnética Transcraneal / Neuroimagen Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Brain Mapp Asunto de la revista: CEREBRO Año: 2019 Tipo del documento: Article País de afiliación: Australia