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临床试验/NCT00001486
NCT00001486已完成不适用

A Neurobiological Investigation of Patients With Schizophrenia Spectrum Disorders and Their Siblings

National Institute of Mental Health (NIMH)1 个研究点 分布在 1 个国家目标入组 4,914 人开始时间: 1995年7月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
4,914
试验地点
1
主要终点
Genetic Polymorphisms affect phenotypes

研究概览

简要总结

This large ongoing study at NIMH investigates the neurobiology of schizophrenia by identifying susceptibility genes, evaluating their impact on brain function to better understand how to treat and prevent this illness.

详细描述

Objective

Schizophrenia is a complex genetic disorder which likely involves many genes each producing a slight increase in risk. Finding weak-acting genes in complex genetic disorders has been challenging and will likely require a number of approaches and large clinical samples. Several strategies have emerged recently that appear to markedly improve the power of genetic studies for detecting such genes. These include using association (rather than linkage) and using intermediate phenotypes in addition to DMS-IV diagnosis.

Study Population: We propose to take advantage of these techniques by studying quantitative traits related to schizophrenia in patients, siblings, and controls.

Design: We will employ an association design, rather than linkage. Traits will include quantifiable neurobiological variables that have been implicated previously as possible phenotypes related to schizophrenia. These include tests of attention and cognition.

Outcome Measure: We will use several statistical methods to show that specific genetic polymorphisms affect these phenotypes, including case control and family based association studies.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • INCLUSION/

排除标准

  • Inclusion criteria for Siblings (probands and unaffected siblings):
  • Probands must have a DSM IV-R diagnosis of schizophrenia,schizoaffective disorder, psychosis N.O.S. or schizophreniform disorder.
  • Probands and Siblings must be between the ages of 18 and 55
  • Probands and Siblings must be free of major medical illnesses, but may have controlled hypertension, thyroid disease, or diabetes.
  • Probands and Siblings must have the cognitive ability to consent for themselves. Those who are judged to have the cognitive ability to consent for themselves at the time of participation, but do not have the legal capacity to consent for themselves may participate if the legal guardian /Legal authorized representative (LAR) provides consent by signing the informed consent form.
  • Fluency in English is required.
  • Exclusion Criteria for Siblings (probands and unaffected siblings):
  • Seizure disorder, mental retardation, organic brain damage or other neurological disease.
  • History of any (excepting nicotine-related) DSM5-defined moderate to severe substance use disorder (or DSM-IV-defined substance dependence).
  • Cumulative lifetime history of any (excepting nicotine-related) DSM5-defined mild substance use disorder (or any DSM-IV-defined substance abuse), either in excess of 5 years total or not in remission for at least 6 months.
  • Head trauma with loss of consciousness over 5 minutes from all but genetic sampling.
  • Chemotherapy.
  • NIMH employees/staff and their immediate family members will be excluded from the study per NIMH policy
  • Siblings who do not qualify for the 2-day or 1-day study, may participate in the limited phenotyping arm in which only a psychiatric interview and a blood draw for genetic analysis (SCID-DNA) will be performed, case control analysis or be included as part of a trio (one parent, one sibling, one patient) to study genetic transmission from parents to offsprings.. All parents are eligible for the study.
  • Inclusion Criteria. Healthy Volunteers/Controls
  • To be eligible for this research study, healthy volunteers must be:
  • Between the ages of 18 and 55
  • Fluency in English is required
  • Healthy Controls Exclusion Criteria:
  • They will not be eligible if:
  • They have history of DSM IV-R psychiatric diagnosis or severe chronic medical illness at the time of the study.
  • They have a history of any (excepting nicotine-related) DSM5-defined moderate to severe substance use disorder (or DSM-IV-defined substance dependence).
  • They have a cumulative lifetime history of any (excepting nicotine-related) DSM5-defined mild substance use disorder (or any DSM-IV-defined substance abuse), either in excess of 5 years total or not in remission for at least 6 months.
  • They may not be eligible for the 2-day or 1-day study if they have a first-degree relative with history of schizophrenia spectrum disorders. However, they may be included in the SCID_DNA or case control analyses.
  • Healthy volunteers must be free of learning disabilities.
  • NIMH employees/staff and their immediate family members will be excluded from the study per NIMH policy.

研究组 & 干预措施

Parents

Parents of Probands and siblings for the purposes of DNA collection

Normal Controls

Male and female adult healthy volunteers

Probands

Adult Subjects with Schizophrenia Spectrum Disorders

Siblings

Adult siblings of Probands

结局指标

主要结局

Genetic Polymorphisms affect phenotypes

时间窗: At time of study participation

genotyping analysis

次要结局

  • PANSS, AIMS, GAF(At time of study participation)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (1)

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