Biological Implications of the Overlapping Phenomenon Between Childhood Schizophrenia and Autism Spectrum Disorders-Heterogeneity Approach Rather Than Diagnostic Boundary

NCT ID: NCT06063525

Last Updated: 2023-10-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

230 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-02-02

Study Completion Date

2024-12-31

Brief Summary

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Complex diseases such as schizophrenia and autism are heterogeneous in clinical presentation and etiology. This high heterogeneity constitutes the challenges for the clinical diagnosis and etiological research, resulting in that the majority of research findings cannot be replicated in the independent samples. For the high comorbid rate between the diagnoses of schizophrenia and autism spectrum disorders (ASD), and the shared neurocognitive deficits, genetic risks, and biological markers between the two disorders, a heterogeneity approach may probably be more promising than to arbitrarily split the two diagnostic categories apart or lump them together for etiological research. In schizophrenia, patients with a very early onset of disease and with preceding neurodevelopmental conditions may imply a different underlying etiology from those with typical onset and without neurodevelopmental conditions. Echoing the evidence that in early onset Parkinson's disease, PARK2 (encoding parkin protein) mutations are successfully reported to be as frequent as 49% with an autosomal-recessive mode of inheritance , representing a specific disease entity of Parkinson's disease. Therefore, it is critical to characterize the clinical phenotypes for this subpopulation of very early onset patients, including their clinical manifestation, disease course, and treatment response, as well as early developmental history and morphological characteristics. These may establish an important base for investigating the etiology and providing adequate clinical care for the heterogeneous syndrome of schizophrenia

Detailed Description

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Conditions

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Schizophrenia Autism Spectrum Disorder

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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childhood onset schizophrenia (COS)

diagnosis of schizophrenia under the age of 13 years.

Structural anatomy

Intervention Type OTHER

images acquired with 3T MRI system with 32 channel head coil

schizophrenia (SZ)

patients with schizophrenia with and age of onset later than 13 years

Structural anatomy

Intervention Type OTHER

images acquired with 3T MRI system with 32 channel head coil

autism spectrum disorder (ASD)

dual diagnosis of schizophrenia and ASD, including SZ with ASD, COS with ASD

Structural anatomy

Intervention Type OTHER

images acquired with 3T MRI system with 32 channel head coil

Interventions

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Structural anatomy

images acquired with 3T MRI system with 32 channel head coil

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* SZ group: schizophrenia onset earlier than 12 years old
* COS group: schizophrenia onset later than 12 years old
* ASD group: diagnosed with autism spectrum disorder without schizophrenia
* Dual group: diagnosed with ASD and SZ

Exclusion Criteria

* congenital disease
* major physical diseases
* neurodegenerative disorder
* chromosomal aberration
Minimum Eligible Age

15 Years

Maximum Eligible Age

59 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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201412165RINB

Identifier Type: -

Identifier Source: org_study_id

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