A thyroid receptor co-activator hypothesis for psychosis
A thyroid receptor co-activator hypothesis for psychosis
批准号:
6419797
负责人:
Robert A Philibert
金额:
$17.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-01-01 至 2005-12-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION: (provided by applicant) Schizophrenia is a neurodevelopmental
syndrome that affects approximately 1 percent of the U.S. population and is
characterized by the presence of hallucinations and delusions. Genetic factors
are thought to account for the majority of the vulnerability to illness for
this syndrome. These genetic factors are thought to be composed of major,
moderate ant mild effect loci. The identification and characterization of
genetic factors of even mild effect loci is a critical step in the process of
understanding the pathogenesis of this group of disorders.
In prior moleular studies, the candidate has identified an exonic polymorphism
(HOPA12bP) in a critical portion of a gene for a thyroid receptor co-activator
named HOPAthat is associated with a behavioral endophenotype that include
schizophrenia and hypothyroidism. In this five year training grant, the
candidate proposes to focus on the behavioral syndrome that is associated with
the polymorphism and 1) demonstrate segregation of the polymorphism with
illness. 2 refine the phenotype associated with the polymorphism, and 3)
identify other mutations that may be related to illness.
Scientific Aims of this grant are 1). Peform case control analyses on
schizophrenic probands with the HOPA12bp polymorphism. Schizophrenic HOPA
probands will be identified and compared to matched case controls for
cognitive/behavioral, endocrinological and medical differences. 2. Conduct a
focused linkage study of the families of HOPA12bp probands. Structured
interviews will be used to assess the presence of cognitive/behavioral and
medical co-morbidity in the first-degree relatives of control and HOPA12bP
probands. These results will be correlated with genetic status. 3). Conduct
SSCP analysis across the HOPA Gene to detect other potentially pathogenic
mutations. Mutation analysis will be performed using DNA from other
schizophrenic patients to detect other mutations in theHOPA gene that can
result in result in this syndrome or related phenotypes.
Training Aims of this grant are to 1) develop clinical skills in the diagnosis
and standardized measurement of complex behavior and endocrinological
disorders, and 2) learn medical and psychiatric epidemiology, ethics, and
biostatistical approaches to complex disorders. The net effect will be to
produce an independent investigator capable of functional and translational
research.
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海外基金