Characterizing Dopamine Receptor Binding in Treatment Resistant Depression

NCT ID: NCT03537794

Last Updated: 2024-08-20

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 45 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-12-31
• Study Completion Date: 2027-12-31

Brief Summary

It is estimated that 30% of individuals with Major Depressive Disorder (MDD) fail to respond to conventional antidepressant medication which accounts for over 1 million Canadians in their lifetime. Treatment resistant depression (TRD) patients also have greater psychiatric and medical comorbidity, poorer quality of life and increased suicidal ideation. Yet, there are few treatment strategies available to target TRD and there is a significant lack of evidence about how TRD differs from treatment-responsive depression. This proposal represents the first study to elucidate the neurobiology of TRD with a focus on dopamine receptor function throughout the brain, in order to inform treatment development and clinical characterization of TRD.The ultimate goal of this unique study is to characterize striatal and extrastriatal dopamine D2 and D3 receptor binding potential in patients with TRD, non-resistant MDD and healthy controls. The primary hypothesis is that TRD patients will exhibit greater D2/D3 receptor binding potential compared to non-TRD patients in the following regions of interest: dorsolateral prefrontal cortex, orbitofrontal cortex, and ventral striatum. Secondarily, non-TRD patients will also demonstrate increased binding potential compared to healthy controls in the same brain regions. Whole brain analyses will allow us to take an exploratory approach to other brain regions that may differentiate TRD from non-TRD patients. Participants will be assessed at St. Michael's Hospital (SMH) and the Centre for Addiction and Mental Health (CAMH), which are within a 10 minute driving distance of each other. There will be 3 study visits following written informed consent. Eligibility will be confirmed at a screening visit at SMH where demographic information, including age, sex, education, and medication history will be obtained, as well as the administration of a structured Mini-International Neuropsychiatric Interview (MINI) for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) Axis I diagnoses (Sheehan et al, 2015), and an HRSD-17. Within two weeks of the screening visit, participants will undergo a structural magnetic resonance imaging (MRI) scan at SMH prior to the positron-emission tomography (PET) scan at CAMH. The order of the PHNO scans will be counterbalanced.

Conditions

Treatment Resistant Depression

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Treatment Resistant Depression

Unmedicated Individuals with Treatment Resistant Depression

PET scans

Intervention Type: DIAGNOSTIC_TEST

PET scans and PHNO scans

Major Depressive Disorder

Unmedicated Individuals with Major Depressive Disorder

PET scans

Intervention Type: DIAGNOSTIC_TEST

PET scans and PHNO scans

Healthy Control

healthy controls with no previous psychiatric disorders

PET scans

Intervention Type: DIAGNOSTIC_TEST

PET scans and PHNO scans

Interventions

PET scans

PET scans and PHNO scans

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• DSM-5 criteria for a Major Depressive Episode (MDE) within a MDD, confirmed through MINI diagnosis (Sheehan et al, 2015)
• Age between 25 and 55 years
• Hamilton Depression Rating Scale - 17 item (HRSD-17; Hamilton, 1960) > 14 (moderate to severe symptoms)
• Free of psychotropic medications for at least 5 half-lives before PET scanning
• Ability to undergo MRI scanning (absence of metal, pacemakers, etc.)
• For non-resistant patients: Previous history of response to an antidepressant, in order to increase signal to noise between resistant and non-resistant patients

• Ages between 25 and 55 years
• Ability to undergo MRI scanning (absence of metal, pacemakers, etc.)

Exclusion Criteria

• Pregnancy/lactation
• Medical condition requiring immediate investigation or treatment
• Recent (< 6 months)/current history of drug abuse/dependence
• Lifetime history of psychosis, other Axis I comorbidities are allowable
• Use of any psychotropic use within 5 half-lives before the PET scanning
• For non-resistant patients: Failure of > 2 antidepressant treatments of adequate dose and duration for current MDE.

• Pregnancy/lactation
• Medical condition requiring immediate investigation or treatment
• Lifetime history of any psychiatric disorder
• Lifetime history of receiving an antidepressant

• Minimum Eligible Age: 25 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre for Addiction and Mental Health

OTHER

Sponsor Role: collaborator

Unity Health Toronto

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Sakina Rizvi, PhD

Role: PRINCIPAL_INVESTIGATOR

Unity Health Toronto

Central Contacts

Sakina Rizvi, PhD

Role: CONTACT

rizvis@smh.ca

416-864-6060 ext. 6489

Ariel Graff-Guerrero, MD, PhD

Role: CONTACT

ariel.graff@camh.ca

416-535-850 ext. 34834

Other Identifiers

TPET-01

Identifier Type: -

Identifier Source: org_study_id