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Improvement of diagnosis of major depressive and bipolar disorder: an fMRI-study.

Diagnostic Imaging of Affective Disorders using Emotion processing (DIADE). A neuroimaging study to determine biomarkers to discriminate between unipolar and bipolar depression.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21341
Enrollment
80
Registered
2009-04-17
Start date
2008-10-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

major depressive disorder bipolar disorder diagnosis fMRI

Interventions

1. Questionnaire
2. Psychiatric interview
3. Affective neuropsychological testing
4. fMRI
5. Venapunction.

Sponsors

AMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Major depressive disorder (MDD) and Bipolar I and Bipolar II (BD I and BD II) patiens of both sexes; 2. Age 18-60 years; 3. Various levels of depressive symptomatology, ranging from moderate to severe (HDRS score at least 16); 4. At least 2 major depressive episodes, with remission between episodes; 5. Age of first episode younger than 40 years; 6. Illness duration of at least 5 years since first episode. In addition, for BD I and BD II: 7. At least one (hypo)manic episode (assessed by SCID) not solely during the use of antidepressants; Healthy controls (HC): 1. Age 20-60 years; 2. Euthymia at time of baseline (IDS less than 14).

Exclusion criteria

Exclusion criteria: MDD and BD I and BD II patients: 1. Electroconvulsive therapy within two months before scanning; 2. Current (hypo)mania (YMRS above 8; at study entry or within the previous month before baseline); 3. Atypical depressive symptomatology; 4. Concurrent comorbid axis I diagnosis; 5. A clear clinical diagnosis of cluster B personality disorder; 6. Currently using psychopharmacological medication (antidepressants, anticonvulsants or mood stabilizers stopped less than 2 months before scanning). Incidental benzodiazepine use will be allowed, but must be stopped before scanning. In addition, for MDD: 1. A history of (hypo)manic derailment after antidepressant use; 2. A family history of bipolar disorder. Healty Controls: 1. A lifetime psychiatric diagnosis (axis I, assessed by SCID); 2. A current diagnosis of alcohol or drug dependence; 3. First degree relatives with a history of psychiatric diagnosis; 4. Use of any psychopharmacological agent. All subjects: 1. A history of head trauma or neurological disease; 2. Severe general physical illness; 3. Claustrophobia or implanted metal. objects.

Design outcomes

Primary

MeasureTime frame
We will compare performance on the neuropsychological task between MDD, BD I and HC, measured by reponse time, number of omissions and number of errors. The same outcomes will be examined fot the neuroimaging tasks. We will compare brain responses of fMRI tasks relative to control conditions between MDD, BD and HC. We will compare responses in predefined ventral and dorsal brain regions (dorsolateral prefrontal cortex (PFC), ventral PFC, orbitofrontal, limbic and subcortical regions).

Contacts

Public ContactM.M. Rive
m.m.rive@amc.uva.nl+31 (0)20 8913698

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)