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Expanding Rapid Ascertainment Network of Schizophrenia Families in Taiwan

Expanding Rapid Ascertainment Network of Schizophrenia Families in Taiwan

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01249079
Enrollment
600
Registered
2010-11-29
Start date
2010-10-31
Completion date
Unknown
Last updated
2010-12-01

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

Conditions

Schizophrenia

Brief summary

This proposal responds to Request for Applications RFA-MH-08-131, which seeks applications that propose to enrich pre-existing resources for schizophrenia in the National Institute of Mental Health (NIMH) Human Genetics Initiative and to apply genomic methods to further the investigators understanding of the molecular etiology of the disorder. The overarching aims of this proposal are to quickly and cost-effectively ascertain a large sample of trio families affected by schizophrenia, and to discover causal variants for the disorder in the first family-based genome-wide association study (GWAS) of the disorder. In Taiwan, there is no such kind of policy to support this kind of GWAS study as it is a very expensive study, including collecting large family samples and genome-wide single-nucleotide polymorphism (SNP) scanning. The investigators, thus, collaborate with Professor Ming T, Tsuang and his entended subcontracted researchers to apply for this project. The investigators, the research team in Taiwan, will collect 3800 trio families (11400 subjects) of schizophrenia. Through additional ascertainment within this framework, the investigators will collect an aggregate sample with adequate power for detecting in a GWAS those variants that make even small contributions to the risk for the disorder. The investigators will meet the overarching goals of this project by accomplishing several Specific Aims, as follows: 1) Rapidly ascertain schizophrenia trio families from Taiwanese clinical ascertainment sites; 2) Supplement NIMH Genetics Initiative collections by sending all clinical data and biomaterials to the appropriate repositories; 3) Assess the association of schizophrenia with a genome-wide panel of single-nucleotide polymorphisms (SNPs) and their constituent haplotypes; 4) Analyze quantitative schizophrenia phenotypes such as age at onset ; 5) Perform a genome-wide survey for copy-number variations related to schizophrenia; 6) Test for gene-gene interactions (epistasis); and 7) Test for gene-environment interactions, such as the well-established effect of season of birth.

Interventions

No intervention would be provided in this research,but need to draw blood

Sponsors

National Taiwan University Hospital
CollaboratorOTHER
China Medical University Hospital
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED

Eligibility

Sex/Gender
ALL
Age
16 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* clinical diagnosis of schizophrenia and their parents, and parents are still alive

Exclusion criteria

* person with Mental Retardation * persons with epilepsy * alcohol or substance abuse combined * in combination with other organic brain damage syndrome

Countries

Taiwan

Contacts

Primary ContactHai-Gwo Hwu
haigohwu@ntu.edu.tw886-2-23122453

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026