Identifying response and predictive biomarkers for Transcranial magnetic stimulation outcomes: protocol and rationale for a mechanistic study of functional neuroimaging and behavioral biomarkers in veterans with Pharmacoresistant depression

• Published in: BMC psychiatry Vol. 21; no. 1; p. 35
• Main Authors: Williams, Leanne M, Coman, John T, Stetz, Patrick C, Walker, Nicole C, Kozel, F Andrew, George, Mark S, Yoon, Jong, Hack, Laura M, Madore, Michelle R, Lim, Kelvin O, Philip, Noah S, Holtzheimer, Paul E
• Format: Journal Article
• Language: English
• Published: England BioMed Central 13-01-2021; BMC
• Subjects: Behavior; Biomarkers; Cognitive ability; Depression; Depressive Disorder, Major - diagnostic imaging; Depressive Disorder, Major - therapy; Dorsolateral prefrontal cortex (DLPFC); Functional magnetic resonance imaging; Functional magnetic resonance imaging (fMRI); Functional Neuroimaging; Humans; Hypotheses; Magnetic fields; Magnetic Resonance Imaging; Major depressive disorder (MDD); Medical imaging; Mental depression; Neural networks; Neuroimaging; Neurosciences; Prefrontal cortex; Prefrontal Cortex - diagnostic imaging; Psychiatry; Quality of Life; Repetitive Transcranial magnetic stimulation (TMS); Study Protocol; Suicides & suicide attempts; Transcranial Magnetic Stimulation; Treatment resistant depression (TRD); Veterans; Neuroimaging; Cognitive control network; Repetitive Transcranial magnetic stimulation (TMS); Biomarker; Dorsolateral prefrontal cortex (DLPFC); Veterans; Major depressive disorder (MDD); Default mode network (DMN); Functional magnetic resonance imaging (fMRI); Treatment resistant depression (TRD)
• ISSN: 1471-244X; 1471-244X
• DOI: 10.1186/s12888-020-03030-z

Although repetitive transcranial magnetic stimulation ('TMS') is becoming a gold standard treatment for pharmacoresistant depression, we lack neural target biomarkers for identifying who is most likely to respond to TMS and why. To address this gap in knowledge we evaluate neural targets defined by activation and functional connectivity of the dorsolateral prefrontal cortex-anchored cognitive control circuit, regions of the default mode network and attention circuit, and interactions with the subgenual anterior cingulate. We evaluate whether these targets and interactions between them change in a dose-dependent manner, whether changes in these neural targets correspond to changes in cognitive behavioral performance, and whether baseline and early change in neural target and cognitive behavioral performance predict subsequent symptom severity, suicidality, and quality of life outcomes. This study is designed as a pragmatic, mechanistic trial partnering with the National Clinical TMS Program of the Veteran's Health Administration.
Target enrollment consists of 100 veterans with pharmacoresistant Major Depressive Disorder (MDD). All veterans will receive a clinical course of TMS and will be assessed at 'baseline' pre-TMS commencement, 'first week' after initiation of TMS (targeting five sessions) and 'post-treatment' at the completion of TMS (targeting 30 sessions). Veterans will be assessed using functional magnetic resonance imaging (fMRI), a cognitive behavioral performance battery, and established questionnaires. Multivariate linear mixed models will be used to assess whether neural targets change with TMS as a function of dose (Aim 1), whether extent and change of neural target relates to and predicts extent of behavioral performance (Aim 3), and whether extent of neural target change predicts improvement in symptom severity, suicidality, and quality of life (Aim 3). For all three aims, we will also assess the contribution of baseline moderators such as biological sex and age.
To our knowledge, our study will be the first pragmatic, mechanistic observational trial to use fMRI imaging and cognitive-behavioral performance as biomarkers of TMS treatment response in pharmacoresistant MDD. The results of this trial will allow providers to select suitable candidates for TMS treatment and better predict treatment response by assessing circuit connectivity and cognitive-behavioral performance at baseline and during early treatment.
ClinicalTrials.gov NCT04663481 , December 5th, 2020, retrospectively registered. The first veteran was enrolled October 30th, 2020.