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Adolescent Neural Substrates of Risk for Schizophrenia

Adolescent Neural Substrates of Risk for Schizophrenia
青少年精神分裂症风险的神经基质
批准号:
7068105
负责人:
ISABELLE M ROSSO
金额:
$13.27万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-06-01 至 2010-05-31

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供):本职业发展计划的主要目标是为应聘者提供培训、支持和资源,使其成为神经精神病学研究领域的一名独立研究员。候选人的长期目标是通过建立一个结合流行病学、发育和神经成像方法的多学科研究计划,促进对精神分裂症发育性神经病理学的了解。候选人在获奖期间的短期目标是发展以下领域的专业知识:(1)磁共振成像(MRI)研究的方法、设计和分析;(2)认知神经科学和神经心理学;(3)纵向研究方法和设计。这些培训目标将通过课程作业、咨询这些领域的知名研究科学家以及在麦克莱恩医院脑成像中心完成研究研究计划的综合计划来实现。这项拟议研究的设计和假设是基于越来越多的工作(包括候选人之前的研究),表明遗传和产科因素可能会以易患精神分裂症的方式扰乱大脑发育。也有初步证据表明,精神病在青春期晚期开始的特征时间可能与这一时期发生在前额叶和颞缘皮质的成熟大脑变化有关。因此,该研究计划建议对精神分裂症遗传风险高(HR)和低(LR)的青少年进行纵向病例对照调查。这项研究的第一个主要目的是考察遗传风险状态和OCS对认知功能的神经心理测量和局部脑体积的结构MRI测量的预测的贡献。第二个主要目标是评估HR和LR受试者在基线和两年随访评估之间大脑结构和认知功能的年龄相关变化。这项研究的结果有望增加我们对青春期标准化脑成熟变化的理解,尽管它与精神分裂症和其他神经精神障碍有潜在的相关性,但一直是一个相对较少的研究领域。此外,这项研究与精神分裂症的病理生理学和疾病高危个体的病前识别有关。
英文摘要
DESCRIPTION (provided by applicant): The principal aim of this career development plan is to provide the candidate with the training, support, and resources required to develop as an independent investigator in the field of neuropsychiatric research. The candidate's long-term goals are to advance knowledge of the developmental neuropathology of schizophrenia by establishing a multidisciplinary research program that combines epidemiologic, developmental, and neuroimaging methods. The candidate's short-term goals for the duration of this award are to develop expertise in the following areas: (1) methods, design, and analysis of magnetic resonance imaging (MRI) studies; (2) cognitive neuroscience and neuropsychology; (3) longitudinal research methods and design. These training goals will be met through a combined program of coursework, consultation with established research scientists in these fields, and completion of a research study plan at McLean Hospital's Brain Imaging Center. The design and hypotheses of the proposed study were based on a growing body of work (including the candidate's prior research) indicating that genetic and obstetric factors may disrupt brain development in a manner that predisposes to schizophrenia. There is also preliminary evidence that the characteristic timing of psychosis onset in late adolescence may relate to maturational brain changes that occur around this period in prefrontal and temporal-limbic cortices. Accordingly, the research plan proposes a longitudinal, case-control investigation of adolescents at high (HR) and low (LR) genetic risk for schizophrenia. The first major aim of the study is to examine the contributions of genetic risk status and OCs to the prediction of neuropsychological measures of cognitive function and structural MRI measures of regional brain volume. The second major aim is to assess age-related changes in brain structure and cognitive function between the baseline and 2-year follow-up assessments in the HR and LR subjects. The results of this study are expected to increase our understanding of the normative brain maturational changes of adolescence, which has been a relatively under-studied area despite its potential relevance to schizophrenia and other neuropsychiatric disorders. In addition, this study has relevance to the pathophysiology of schizophrenia and to the premorbid identification of individuals at heightened risk for the disorder.
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