Treatment Resistant Depression
Conditions
Brief summary
Background: Theta-burst stimulation (TBS), a form of repetitive transcranial magnetic stimulation (rTMS) holds promise as an effective treatment for treatment resistant depression (TRD). rTMS has been linked to neuroplastic changes as shown using magnetic resonance imaging (MRI) and positron emission tomography (PET). Alterations in serotonin-1A receptor expression (5-HT1A) have been linked to major depression. Moreover, changes in 5-HT1A receptor binding - observed after pharmacological treatment, as well as after electroconvulsive therapy - has been linked to neuronal adaptations in response to these antidepressant treatments. Objectives of the study: Here, the aim is to investigate the effects of TBS over left and right dorsolateral prefrontal cortex on the 5-HT1A receptor binding in patients with TRD using PET. In addition, effects of iTBS on brain structure and function will be determined using functional, structural and perfusion MRI. Study population: 80 patients with TRD who maintain their original medication regimen will be recruited. Study design: Longitudinal, randomized and double-blind clinical trial. 40 patients will receive active TBS, 40 patients will receive sham TBS for treatment duration of three weeks. Before and after three weeks of treatment, patients will be scanned using MRI and PET with the highly specific and selective radiotracer \[carbonyl-11C\]WAY100635. A follow-up visit and final examination will be performed 2 and 4 weeks after treatment for the active TBS group, respectively. Patients in the sham TBS arm will receive active TBS treatment immediately after the second MRI and PET scan. Relevance and implications of the study: This will be the worldwide first multimodal imaging study to investigate the effects of TBS on serotonin-1A receptor binding in TRD using PET. Thus, the study will add crucial knowledge to the existing literature on the effects of TMS on brain structure and function, related to antidepressant efficacy. Moreover, by combining molecular imaging of serotonergic neurotransmission with structural and functional MRI, the proposed study will increase the investigators knowledge on the serotonergic role in shaping brain morphology, microstructure and structural/functional connectivity. Taken together, the study has the potential to contribute to the development of personalized treatment, the reduction of personal suffering and the reduction of costs and occupational disability.
Interventions
DEVICEtheta-burst stimulation using a MagPro X1000
TBS over left and right dorsolateral prefrontal cortex for a period of three weeks. iTBS over left DLPFC: 3-pulse 50 Hz bursts will be given every 200ms (at 5 Hz) in 2-second trains with an inter-train interval of 8 seconds. Trains will be repeated 20 to reach a total number of 600 pulses per session. cTBS over right DLPFC: cTBS will comprise uninterrupted bursts to reach a total number of 600 pulses per session. Two sessions per day, separated by 60 minutes; 30 Sessions in total over 3 weeks.
DEVICEsham stimulation using a MagPro X1000
Sham TBS with the coil set at 45° against the skull will be performed over left and right dorsolateral prefrontal cortex for a period of three weeks
Sponsors
Rupert Lanzenberger
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* DSM-5 diagnosis of single or recurrent major depression * HAMD-17 total score of ≥ 18 and a Clinical Global Impression Scale (CGI-S) of ≥ 4 * Failure of at least two adequate antidepressant treatments * Age 18-65 years * Right-handedness (assessed with the Edinburgh Handedness Inventory)
Exclusion criteria
* Seizures in medical history * Lifetime medical history of major systemic illness, neurological disorders and previous brain injuries * Ferromagnetic implants, cardiac pacemaker, deep brain stimulation and other common MRI
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Regional 5-HT1A receptor binding | before and after 3 weeks of TBS treatment | 5-HT1A receptor binding using the radioligand \[carbonyl-11C\]WAY100635 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Regional white matter microstructure using DWI-Tractography | before and after 3 weeks of TBS treatment | Tractography will be performed |
| Regional grey matter volume using MRI | before and after 3 weeks of TBS treatment | The analysis will be done using voxel-based morphometry |
| Regional brain perfusion | before and after 3 weeks of TBS treatment | Regional brain perfusion will be evaluated using Arterial Spin Labeling, ASL |
| Functional connectivity at rest and during tasks | before and after 3 weeks of TBS treatment | Functional connectivity will be evaluated using resting state and task fMRI |
| Regional white matter microstructure using DWI-TBSS | before and after 3 weeks of TBS treatment | The analysis will be performed using tract-based spatial statistics |
Other
| Measure | Time frame | Description |
|---|---|---|
| Global physical activity | before and after 3 weeks of TBS treatment | assessed using the WHO global physical assessment GPAQ |
| Depression score using the Beck Depression Inventory | before and after 3 weeks of TBS treatment | Depression will be evaluated using the Beck Depression Inventory |
| Depression score using the Hamilton Depression Rating Scale | before and after 3 weeks of TBS treatment | Depression will be evaluated using the Hamilton Depression Rating Scale |
Countries
Austria
Contacts
Primary ContactRupert Lanzenberger, MD
Backup ContactGeorg Kranz, PhD
Outcome results
None listed