Major Depressive Disorder, Suicidal Ideation, Suicide
Conditions
Brief summary
The ultimate aim of this study is to identify a biomarker of suicide risk in MDD by measuring the "hedonic spectrum" (pain and reward responsivity), attention and its associated brain structures using brain scans (fMRI and DTI), as well as the stability of markers over time.
Detailed description
The issue of suicide has continued to puzzle researchers in the field of psychiatry. Edwin Shneidman, a prominent researcher on suicide emphasized "the most evident fact about suicidology and suicidal events is that they are multidimensional…containing concomitant biological, sociological, and psychological (interpersonal and intrapsychic)…elements". Yet, no study to date has attempted to integrate these dimensions when evaluating suicide risk. Considering the presence of a psychiatric illness is a primary predictor of suicide, it is important to develop a unified understanding of risk factors that integrate current clinical and neurobiological findings in this population. Our aim is to: (1) identify an integrated biomarker model to predict risk of suicide attempt in patients with Major Depressive Disorder (MDD) with and without a history of suicide attempt, using neuroimaging, neurocognitive testing and behavioural tasks, and (2) test the stability of this model using a prospective 1 year design.
Interventions
OTHERNo intervention
Sponsors
Unity Health Toronto
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
1. DSM-5 criteria for Major Depressive Episode within a MDD, confirmed through MINI diagnosis104 2. Ages between 18 and 70 years 3. Hamilton Depression Rating Scale - 17 item (HAMD-17) \>= 14 4. Capable of giving informed consent 5. Groups 1 and 2 participants only: HAMD-17 item 3 (suicide) \>= 2 6. Group 2 participants only: positive history of a suicide attempt within the last six months 7. Group 3 participants only: positive history of a lifetime suicide attempt
Exclusion criteria
1. Pregnancy/lactation 2. Medical condition requiring immediate investigation or treatment 3. Recent (\< 6 months)/current history of drug abuse/dependence (other than caffeine, or nicotine) 4. Lifetime history of psychosis, Bipolar I or Bipolar II; other Axis I comorbidities are allowable 5. Individuals who are taking a daily sedative hypnotic, atypical antipsychotic or stimulant must be on a stable dose for at least 4 weeks prior to the neuroimaging scan. The dose must not be taken after 10:00pm the evening prior to the scan. Those receiving a benzodiazepine or an atypical antipsychotic on an "as needed" basis (taken, but not every day) will be washed out of their benzodiazepine/atypical antipsychotic for two weeks prior to neuroimaging. Those receive stimulants on an "as needed" basis will be washed out for 1-3 days prior to neuroimaging, depending on the stimulant half-life. 6. Participation in experimental treatment trials for the study duration.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Biomarkers for Suicide Risk | 12 months | Potential biomarkers for suicide risk including brain scans, genomic or proteomic makers, |
Countries
Canada
Contacts
PRINCIPAL_INVESTIGATORSakina Rizvi, PhD
Unity Health Toronto
Outcome results
None listed