Major Depressive Disorder
Conditions
Brief summary
Selective serotonin reuptake inhibitors (SSRIs) raise serotonin (5-HT) in the synaptic cleft and are the current first line of pharmacological antidepressive treatment. Yet, there is a missing link between this first molecular step in their mechanism of action and observed clinical improvement. We have determined to establish a framework combining genuine molecular and functional imaging, i.e. hybrid pharmaco-PET/MR imaging, of the human serotonergic system in order to predict antidepressant treatment response. Objectives: 1. To predict antidepressant treatment response from data obtained using hybrid PET/MR with acute pharmacological challenge. 2. To discriminate healthy from depressed subjects using this paradigm. 3. To establish models connecting regional changes in occupancy of serotonin transporters (5-HTT) following citalopram infusion, with changes in brain activation and connectivity of major resting-state hub networks. Design: Randomized, double-blind, placebo-controlled, cross-over mono-center study. Materials and methods: 40 major depressed (MDD) and 40 healthy subjects will undergo 2 PET/MR scans on a 3T SIEMENS mMR Biograph scanner: 1. challenge with citalopram 8mg 2. placebo (saline). After structural imaging, functional MRI will be continuously acquired. \[11C\]DASB will be applied using a bolus + constant infusion paradigm to probe 5-HTT binding potentials and monitor 5-HTT occupancy with drug challenge, applied after 70min, in a single session. Scanning will be terminated 80min after challenge. MDD patients will receive subsequent escitalopram treatment with repeated evaluation of response for 3 months.
Interventions
2 PET/MR scans will be performed (placebo/citalopram - double-blind randomized cross-over)
8mg citalopram or placebo (saline) will be applied during PET/MR measurements in a double-blind randomized cross-over design
After completion of imaging procedures, patients will receive treatment with escitalopram 10-20mg. In case of non-response, after 6 weeks, treatment will be switched to either Mirtazapine, Duloxetine or Venlafaxine
8mg citalopram or placebo (saline) will be applied during PET/MR measurements in a double-blind randomized cross-over design
Sponsors
Study design
Eligibility
Inclusion criteria
* General health based on medical history, physical examination and structured clinical interview for DSM-IV (SCID) * HAM-D≥18 (patients) * Willingness and competence to sign the informed consent form * Age 18 to 55 years
Exclusion criteria
* Any medical, psychiatric or neurological illness (other than MDD) * Current or former psychopharmacological treatment * Current or former substance abuse * Pregnancy * Any implant or stainless steel graft or any other contraindications for MRI * Failure to comply with the study protocol or to follow the instructions of the investigating team * Participation in studies involving radiation exposure in the past 10 years. * Body mass index \<17 or \>30
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hamilton Depression Scale (HDRS) | 12 weeks |
Countries
Austria