课题基金 / 基金详情

Genetic Screen for Antipsychotic Drug Response

Genetic Screen for Antipsychotic Drug Response
抗精神病药物反应的基因筛查
批准号:
6846303
负责人:
David Pickar
金额:
$47.7万
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:
2002-09-25 至 2006-12-31

项目摘要

项目成果

David Pickar的其他基金

相关文献

中文摘要
翻译
描述(由申请人提供):精神分裂症是最严重的精神障碍,困扰着1%的人口,给患者及其家人带来痛苦,并最大限度地扩展医疗资源。通过基因、药理等技术改善精神疾病患者的治疗和保健是Gabriel Pharma的使命。该补助金的主要目标是建立抗精神病药物反应的遗传筛查和精神分裂症结局的遗传预测因子,从而实现个性化治疗和资源分配。本提案描述了第I阶段引入的交互式临床信息和DNA数据库(CI-DNA)的原理、设计和科学发展。CI数据库将扩展为包括两个用于药物遗传学分析的药理学数据库组件和一个用于遗传预测分析的首个精神分裂症临床结局数据库。第一阶段成功地开发了氯氮平药物遗传学数据库的临床部分。作为I期可行性研究的一部分,Gabriel Pharma首次建立了氯氮平阴性症状反应的遗传预测因子。在II期,将对扩展数据库中的受试者进行一组10种功能候选基因变体的基因分型。选择这些基因是因为它们与中枢神经系统(CNS)、精神分裂症和抗精神病药物机制的关系。此外,三个最近发现的精神分裂症易感基因将在数据库中进行检查。完全开发的专有CI-DNA数据库系统是一项独特的创新,通过内部和协作的科学努力,能够建立抗精神病药物反应和精神分裂症结果的遗传筛查。这项工作有可能影响个别精神分裂症患者以及相关医疗保健服务的更广泛需求。
英文摘要
DESCRIPTION (provided by applicant): Schizophrenia, the most serious of the mental disorders, afflicts 1% of the population, causing suffering to patients and their families and stretching health care resources to a maximum. It is the mission of Gabriel Pharma to improve the treatment and health care for patients with mental illnesses through genetic, pharmacological and other technologies. A primary goal of this grant is to establish a genetic screen for antipsychotic drug response and genetic predictors of outcome of schizophrenia, enabling an individualized approach to treatment and resource allocation. This proposal describes the rationale, design and scientific development of the Interactive Clinical Information and DNA database (CI-DNA) introduced in Phase I. The CI-Database will be expanded to include two pharmacological database components designed for pharmacogenetics analysis and a first-of-its-kind clinical outcome database for schizophrenia designed for genetic predictor analysis. Phase I successfully developed the clinical portion of a database for the pharmacogenetics of clozapine. As part of the Phase I feasibility study Gabriel Pharma established, for the first time, genetic predictors of negative symptom response to clozapine. In Phase II, subjects in the expanded database will be genotyped for a panel of ten functional candidate gene variants. These genes are chosen for their relationship to the central nervous system (CNS), schizophrenia and antipsychotic drug mechanisms. In addition, three recently discovered schizophrenia susceptibility genes will be examined in the database. The fully developed proprietary CI-DNA database system is a unique innovation enabling the establishment of genetic screens for antipsychotic drug response and schizophrenia outcome through internal and collaborative scientific efforts. This work has the potential of impacting the individual patient with schizophrenia as well as broader needs in related health care delivery.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
Pharmacotherapy of schizophrenic patients: preponderance of off-label drug use.
精神分裂症患者的药物治疗:超说明书用药占多数。
DOI: 10.1371/journal.pone.0003150
发表时间: 2008
期刊: PloS one
影响因子: 3.7
作者: [Pickar,David, Vinik,Jessie, Bartko,JohnJ]
通讯作者: Bartko,JohnJ
SBIR Triple Re-Uptake Inhibitors: Potential Antidepressants
  • 批准号:
    7320678
  • 项目类别:
  • 资助金额:
    $25.0万
  • 财政年份:
    2007
  • 负责人:
    David Pickar
  • 依托单位:
Genetic Screen for Antipsychotic Drug Response
  • 批准号:
    6582268
  • 项目类别:
  • 资助金额:
    $10.0万
  • 财政年份:
    2002
  • 负责人:
    David Pickar
  • 依托单位:
Genetic Screen for Antipsychotic Drug Response
  • 批准号:
    6740490
  • 项目类别:
  • 资助金额:
    $47.7万
  • 财政年份:
    2002
  • 负责人:
    David Pickar
  • 依托单位: