Hersenvocht bij psychiatrische aandoeninge
- Conditions
- Psychosis, schizophrenia, affective disorders, depression
- Registration Number
- NL-OMON26758
- Lead Sponsor
- niversity Medical Center Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 800
Psychotic disorder patients: a DSM-IV or 5 classification of schizophrenia, schizophreniform disorder, schizoaffective disorder (both depressive and bipolar types), psychosis not otherwise specified (or other unspecified psychotic disorders), major depressive disorder with psychotic features, bipolar disorder with current psychotic features or a history of psychotic features and psychosis during the peripartum period (8 weeks after giving birth). DSM-IV or DSM-5 diagnosis will be clinician-rated or based on semi-structured interviews (i.e. the Semi-structured Clinician Interview for DSM Disorders, SCID).
Affective disorder patients: a DSM-IV or 5 classification of unipolar depressive or bipolar disorders without psychotic features. DSM-IV or DSM-5 diagnosis will be clinician-rated or based on semi-structured interviews (i.e. the Semi-structured Clinician Interview for DSM Disorders, SCID).
Patients with psychotic or affective disorders
Subjects meeting any of the following criteria will be excluded from participation in this study:
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method CSF constituents:<br /><br>-Autoantibodies to CNS receptors.<br /><br>-A panel of cytokine, chemokine and growth factor levels.<br /><br>-MiRNA levels. <br /><br>-Neurotransmitter concentrations (including GABA, glutamate and all major amino acids).<br /><br>- Plasma: Plasma levels of the CSF constituents mentioned under primary parameters.<br /><br>- Genetic assessments: To unravel the contribution of genetic variation to the quantitative phenotypes under investigation here, and thereby potentially aid in the identification of genetic variation underlying psychosis, a hypothesis-driven genetic approach will be adopted.<br /><br>-To link biochemical and genetic data to the behavioral level, we will have participants fill out questionnaires assessing a range of behavioral traits, as mentioned below. <br>
- Secondary Outcome Measures
Name Time Method - Plasma: Plasma levels of the CSF constituents mentioned under primary parameters.<br /><br>- Genetic assessments: To unravel the contribution of genetic variation to the quantitative phenotypes under investigation here, and thereby potentially aid in the identification of genetic variation underlying psychosis, a hypothesis-driven genetic approach will be adopted.<br /><br>-To link biochemical and genetic data to the behavioral level, we will have participants fill out questionnaires assessing a range of behavioral traits, as mentioned below. <br>