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

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

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32689
Enrollment
80
Registered
2008-09-22
Start date
2008-10-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

bipolar disorder depression mood disorders

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Major depressive disorder (MDD) and Bipolar disorder I (BD I) patients of both sexes: age 20-60 years; various levels of depressive symptomatology, ranging from moderate (HDRS * 16), to severe; at least 2 major depressive episodes, with remission between episodes; age of first episode * 30 years; illness duration of * 5 years since the first episode. In addition, for BD I: at least one manic episode (assessed by SCID) not solely during the use of antidepressants. Healthy controls (HC): age 20-60 years; euthymia at time of baseline (IDS * 14)

Exclusion criteria

Exclusion criteria: MDD and BD I patients: electroconvulsive therapy within 2 months before scanning; current (hypo)mania (Young Mania Rating Scale (YMRS) > 8; at study entry or within the previous 4 months before baseline); atypical depressive symptomatology; concurrent co-morbid Axis I diagnosis; a clear clinical diagnosis of cluster B personality disorder (assessed by previous documentation and/or a history of recurrent suicidal and/or parasuicidal acts); currently using psychopharmacological medication (antidepressants, anticonvulsants or mood-stabilizers stopped * 2 months before scanning). Incidental benzodiazepine use will be allowed, but must be stopped before scanning. In addition, for MDD: a history of (hypo)manic derailment after antidepressant use; a family history of bipolar disorder. HC: a lifetime psychiatric diagnosis (axis I, assessed by SCID); a current diagnosis of alcohol or drug dependence; first-degree relatives with a history of a psychiatric diagnosis; use of any psychopharmacological agent. All subjects: a history of head trauma or neurological disease; severe general physical illness; claustrophobia or implanted metal objects.

Design outcomes

Primary

MeasureTime frame
We will compare performance on the affective go/no-go task between MDD, BD I and HC, measured by response time, number of omissions and number of errors. The same outcomes will be examined for 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).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)