Your browser doesn't support javascript.
loading
N100 as a response prediction biomarker for accelerated 1 Hz right DLPFC-rTMS in major depression.
Sheen, Jack Z; Mazza, Frank; Momi, Davide; Miron, Jean-Philippe; Mansouri, Farrokh; Russell, Thomas; Zhou, Ryan; Hyde, Molly; Fox, Linsay; Voetterl, Helena; Assi, Elie Bou; Daskalakis, Zafiris J; Blumberger, Daniel M; Griffiths, John D; Downar, Jonathan.
Afiliación
  • Sheen JZ; Institute of Medical Science, University of Toronto, Toronto, Canada. Electronic address: jack.sheen2018@gmail.com.
  • Mazza F; Institute of Medical Science, University of Toronto, Toronto, Canada; Krembil Centre for Neuroinformatics, Centre for Addiction and Mental Health, Toronto, Canada.
  • Momi D; Krembil Centre for Neuroinformatics, Centre for Addiction and Mental Health, Toronto, Canada.
  • Miron JP; Institute of Medical Science, University of Toronto, Toronto, Canada; Department of Psychiatry, Faculty of Medicine, University of Toronto, Canada; Centre Hospitalier de l'Université de Montréal (CHUM), Centre de Recherche du CHUM (CRCHUM), Montreal, QC, Canada; Département de Psychiatrie, Faculté d
  • Mansouri F; Institute of Medical Science, University of Toronto, Toronto, Canada.
  • Russell T; Krembil Research Institute, University Health Network, Toronto, Canada.
  • Zhou R; Krembil Research Institute, University Health Network, Toronto, Canada.
  • Hyde M; Institute of Medical Science, University of Toronto, Toronto, Canada; Krembil Research Institute, University Health Network, Toronto, Canada.
  • Fox L; Krembil Research Institute, University Health Network, Toronto, Canada.
  • Voetterl H; Research Institute Brainclinics, Brainclinics Foundation, Nijmegen, the Netherlands.
  • Assi EB; Centre de Recherche du CHUM (CRCHUM), Montreal, QC, Canada; Department of Neuroscience, Université de Montréal, Montreal, QC, Canada.
  • Daskalakis ZJ; Institute of Medical Science, University of Toronto, Toronto, Canada; Department of Psychiatry, Faculty of Medicine, University of Toronto, Canada; Temerty Centre for Therapeutic Brain Intervention, Centre for Addiction and Mental Health, Canada; Department of Psychiatry, University of California Sa
  • Blumberger DM; Institute of Medical Science, University of Toronto, Toronto, Canada; Department of Psychiatry, Faculty of Medicine, University of Toronto, Canada; Temerty Centre for Therapeutic Brain Intervention, Centre for Addiction and Mental Health, Canada.
  • Griffiths JD; Institute of Medical Science, University of Toronto, Toronto, Canada; Department of Psychiatry, Faculty of Medicine, University of Toronto, Canada; Krembil Centre for Neuroinformatics, Centre for Addiction and Mental Health, Toronto, Canada.
  • Downar J; Institute of Medical Science, University of Toronto, Toronto, Canada; Department of Psychiatry, Faculty of Medicine, University of Toronto, Canada; Temerty Centre for Therapeutic Brain Intervention, Centre for Addiction and Mental Health, Canada.
J Affect Disord ; 363: 174-181, 2024 Oct 15.
Article en En | MEDLINE | ID: mdl-39033822
ABSTRACT
BACKGROUND AND

OBJECTIVE:

Repetitive transcranial magnetic stimulation (rTMS) is a safe and effective treatment for major depressive disorder (MDD); however, this treatment currently lacks reliable biomarkers of treatment response. TMS-evoked potentials (TEPs), measured using TMS-electroencephalography (TMS-EEG), have been suggested as potential biomarker candidates, with the N100 peak being one of the most promising. This study investigated the association between baseline N100 amplitude and 1 Hz right dorsolateral prefrontal cortex (R-DLPFC) accelerated rTMS (arTMS) treatment in MDD.

METHODS:

Baseline TMS-EEG sessions were performed for 23 MDD patients. All patients then underwent 40 sessions of 1 Hz R-DLPFC (F4) arTMS over 5 days and a follow-up TMS-EEG session one week after the end of theses arTMS sessions.

RESULTS:

Baseline N100 amplitude at F4 showed a strong positive association (p < .001) with treatment outcome. The association between the change in N100 amplitude (baseline to follow-up) and treatment outcome did not remain significant after Bonferroni correction (p = .06, corrected; p = .03, uncorrected). Furthermore, treatment responders had a significantly larger mean baseline F4 TEP amplitude during the N100 time frame compared to non-responders (p < .001). Topographically, after Bonferroni correction, F4 is the only electrode at which its baseline N100 amplitude showed a significant positive association (p < .001) with treatment outcome.

LIMITATIONS:

Lack of control group and auditory masking.

CONCLUSION:

Baseline N100 amplitude showed a strong association with treatment outcome and thus demonstrated great potential to be utilized as a cost-effective and widely adoptable biomarker of rTMS treatment in MDD.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor / Electroencefalografía / Estimulación Magnética Transcraneal / Potenciales Evocados / Corteza Prefontal Dorsolateral Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Affect Disord Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor / Electroencefalografía / Estimulación Magnética Transcraneal / Potenciales Evocados / Corteza Prefontal Dorsolateral Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Affect Disord Año: 2024 Tipo del documento: Article