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Improve diagnosis of psychotic disorder of autoimmune origin

Improve diagnosis of psychotic disorder of autoimmune origin - PSYANTIB (psychosis antibodies)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON53058
Enrollment
100
Registered
2016-06-22
Start date
2017-01-30
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

autoimmunity psychosis

Interventions

None listed

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
16 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Psychotic disorder, defined as one or more of the following symptoms: hallucinations, delusions, thought disorders or catatonia (standardized criteria of the CASH) - Psychotic disorder, defined as one or more of the following symptoms: hallucinations, delusions, thought disorders or catatonia (standardized criteria of the CASH) - Duration of disease shorter than 5 years - At least 16 years of age - Capacity to understand the purpose and details of the study in order to provide written informed consent. Alternatively, in the case of patients during a period of mental instability, the informed consent will be asked from family or a legal representative.

Exclusion criteria

Exclusion criteria: - Other severe brain disease which can interfere in the neurocognitive tests - Presence of other immune disorders with active treatment - Psychosis due to drug abuse

Design outcomes

Primary

MeasureTime frame
The primary outcome measure of this study is the prevalence of autoantibodies to specific neuronal surface ion channel/receptor proteins: NMDA-r, AMPA-r, GABAB-r, LGI1 and Caspr-2, in patients with an early onset stable psychotic disorder with or without autoimmune encephalitis.

Secondary

MeasureTime frame
a) Prediction of the presence of autoantibodies on the basis of clinical symptoms (by comparing clinical cognitive and neurological characteristics of patients with a psychotic disorder with or without an underlying autoimmune antibody). b) Identification of the effector functions of the autoantibodies (in vitro studies). Associate autoantibody effector functions with clinical characteristics. c) Study of the BBB integrity in a descriptive way and correlate these data with the clinical characteristics and the presence of autoantibodies.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)