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Psychiatric co-morbidity in dystonia-(plus) syndromes: is serotonin the common pathway?

Psychiatric co-morbidity in dystonia-(plus) syndromes: is serotonin the common pathway? - Dystonia en Psychiatry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON40547
Enrollment
200
Registered
2014-07-15
Start date
2014-08-13
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

depressieve stemmingsstoornissen en afwijkingen dystonia (there are no synonyms)

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with clinically confirmed diagnosis of idiopathic cervical dystonia (CD) or Carrier of mutation in DYT11 gene for myoclonus-dystonia (MD) or Carrier of mutation in GTP-cyclohydrolase 1 gene for dopa-responsive dystonia (DRD) Only adults ( >= 18 years old) will be eligible for PET-scans

Exclusion criteria

Exclusion criteria: General exclusion criteria: other neurological conditions past of present, treatment with deep brain stimulation ;Additional exclusion criteria from the PET-scanning: - SSRI use in the past 6 months to or during the study - use of medication with a known effect on serotonin receptors or transporters - pregnancy or nursing - exhibition to a radiation dose for other reasons, exceeding the maximum annual dose

Design outcomes

Primary

MeasureTime frame
The main study parameter is the proportion of dystonia patients having psychiatric co-morbidity, compared to the proportion having psychiatric symptoms in a healthy control population (part A), and the percentage difference in serotonin metabolism (serotonin transporter (SERT) on a [11C]DASB PET scan between subjects with dystonia and healthy controls, and between subjects with and without psychiatric disorders (part B). Serotonin metabolism will be assessed as [11C]-DASB binding potential (BP) as outcome measure for SERT availability in different brain regions of interest (ROIs): brainstem, striatum and frontal cortex. Additionally, a whole brain voxelwise comparison will be performed using Statistical Parametric Mapping (SPM).

Secondary

MeasureTime frame
Motor assessment: Severity of dystonia, severity of myoclonic symptoms, clinical severity Psychiatric assessment Adults: the presence of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-VI) diagnosis, Life-time prevalence of any psychiatric diagnosis, severity of anxiety symptoms, severity of panic symptoms, severity of social anxiety symptoms and avoidance, severity of OCD symptoms, severity of depressive symptoms Children: the presence of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-VI) diagnosis Concentrations of serotonin in platelets Genetics: the presence of polymorphisms of 5-HTTLPR (serotonin-transporter-linked polymorphic region), DNA methylation rate of the serotonin transporter gene

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)