Effects of Electroconvulsive Therapy on Serotonin-1A Receptor Binding in Major Depression
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Medical University of Vienna
- Enrollment
- 12
- Locations
- 1
- Primary Endpoint
- serotonin-1A receptor binding potential
Study Overview
Brief Summary
In treatment-resistant depression, electroconvulsive therapy (ECT) has been shown to effectively reduce depressive symptoms, though the underlying neurobiological mechanism is still unclear. The serotonergic system, and in particular the inhibitory serotonin-1A (5-HT1A) receptor, appears to be significantly involved in the effectiveness of ECT. The aim of the study is to assess the effects of ECT on the 5-HT1A receptor binding potential (BPND) and distribution in humans in vivo using positron emission tomography (PET) and the radioligand [carbonyl-11C]WAY-100635.
12 patients suffering from severe, therapy-resistant unipolar depression will undergo 3 PET scans, two of these scans taking place before the ECT treatment, consisting of 6-14 ECTs, the third scan taking place after the ECT treatment.
This imaging study hypothesizes that upon completion of the ECT, the overall 5-HT1A receptor BPND in the brain of depressed patients will significantly change.
This study would be the first to demonstrate an effect of electroconvulsive therapy on the 5-HT1A receptor binding in humans in vivo. Given the involvement of the 5-HT1A receptor in the pathophysiology of mood disorders, the present study would be an important step towards a better understanding of antidepressant treatment and treatment response. By comparing treatment effect and the underlying biological mechanism, the study might help to identify biomarkers that distinguish patients who are likely to benefit from ECT from patients who will rather be non-responders. Finally, by investigating the role of the 5-HT1A receptor in ECT, is highly discussed relevance for antidepressant action will be further elucidated and might prepare the ground for new therapeutic strategies.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Basic Science
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Male or female
- •Age 18 - 65 years
- •ICD-10 diagnosis of severe unipolar depression (ICD-10: F32.2, F32.3; F33.2, F33.3)
- •A score of 23 or greater on the 17-item HAM-D
- •Signed informed consent form
- •Negative urine pregnancy test in women at the screening visit and at PET days
- •Antidepressive and antipsychotic medication in a steady state for at least 10 days prior to inclusion
- •Anesthesiological approval for ECT
Exclusion Criteria
- •Concomitant major internistic or neurological illness
- •Clinically relevant abnormalities on a general physical examination and routine laboratory screening
- •Current substance abuse, addiction
- •Current or past history of schizophrenia or schizoaffective disorder
- •Exposure to artificial radiation as volunteer in clinical studies within 10 years prior to inclusion into the present study
- •Previous treatments with electroconvulsive therapy
- •Treatment (< 1 months before screening) with the following drugs: Aripiprazole, Risperidone, Ziprasidone, Clozapine, Chlorpromazine, Amitryptyline, Nefazodone, Trazodone, Buspirone, Pindolol, Penbutolol, Tertatolol, Alprenolol, Quetiapine
- •Investigations using PET or SPECT within 10 years prior to the inclusion
Arms & Interventions
ECT
Intervention: ECT (Procedure)
Outcomes
Primary Outcomes
serotonin-1A receptor binding potential
Time Frame: 2 months
Secondary Outcomes
No secondary outcomes reported
Investigators
Rupert Lanzenberger
A/Prof. PD Dr.
Medical University of Vienna