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中文摘要
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描述(申请人提供):脑血管疾病是导致老年人痴呆的最常见原因之一。随着西方社会老年人口的增长,血管认知障碍(VCI)将成为21世纪的重大医疗负担。磁共振成像(MRI)的最新进展正在不断降低检测大脑中血管异常的门槛,导致人们越来越意识到小血管疾病和微梗塞可以累积导致VCI。然而,目前MRI的能力受到限制,因为无法明确地将异常MR信号与特定的病变类型联系起来。有效的动物模型将大大加快脑血管疾病的诊断和治疗方法。明确识别MR异常一直是研究脑Aβ-淀粉样血管病(CAA)的一个特殊问题,CAA是一种老年人疾病,错误折叠的A‘肽聚集在脑血管壁中。研究人员越来越多地使用新的成像技术来非侵入性地分析CAA。然而,迫切需要能够解释患者CAA和其他血管疾病的神经影像数据的信息。老年松鼠猴是一种独特的自然发生的CAA的动物模型,与人类的CAA疾病高度相似。我们研究项目的首要目标是阐明CAA在老年人血管功能障碍和认知功能下降中的作用。这项建议的目的是利用这一特殊的灵长类动物模型来优化MRI的能力,以非侵入性地识别和表征活体患者的CAA相关病变。为了实现这一目标,我们首先将在一台强大的(7T)磁共振扫描仪中,研究患有CAA的老年松鼠猴子的独特大脑存档样本,以及患有CAA的人类的死后组织样本。通过这种方式,我们可以在最佳条件下检测各种血管病变。接下来,我们将使用从这些体外成像研究中获得的信息,在体内对一小群老年松鼠猴子进行成像。然后,将对大脑进行显微镜检查,以明确地识别和描述MRI异常,并确定病变的细胞和分子特征。我们预测MRI信号异常将与CAA及其相关病变的特定组织病理学指标相关联。这一新的灵长类动物模型的发现将为未来非侵入性研究老年人CAA的发病机制、诊断和治疗奠定基础。
英文摘要
DESCRIPTION (provided by applicant): Cerebrovascular disease is one of the most common causes of dementia in aging humans. With the growing elderly population in Western societies, vascular cognitive impairment (VCI) will become a significant healthcare burden in the 21st century. Recent advances in magnetic resonance imaging (MRI) are continually lowering the threshold for detection of vascular anomalies in the brain, leading to a growing awareness that small vessel disease and microinfarcts can cumulatively lead to VCI. However, the power of MRI currently is limited by the inability to link anomalous MR signals unambiguously to specific lesion types. Valid animal models would greatly accelerate diagnostic and therapeutic approaches to cerebrovascular disease. The explicit identification of MR anomalies has been a particular problem in investigating cerebral A¿-amyloid angiopathy (CAA), a disease of the elderly in which misfolded A¿ peptide accumulates in the walls of brain blood vessels. Investigators have increasingly employed novel imaging protocols to analyze CAA non-invasively. However, there is a critical need for information that will enable the interpretation of neuroimaging data on CAA and other vascular disorders in patients. The aged squirrel monkey is a unique animal model of naturally occurring CAA that is highly similar to the disorder in humans. The overarching goal of our research program is to clarify the role of CAA in vascular dysfunction and cognitive decline in the elderly. The objective of this proposal is to employ this exceptional primate model to optimize the power of MRI to non-invasively identify and characterize CAA-related lesions in living patients. To achieve this goal, we first will investigate a unique sample of archived brains from aged squirrel monkeys with CAA, along with postmortem tissue samples from humans with CAA, in a powerful (7T) MRI scanner. In this way, we can detect a variety of vascular lesions under optimal conditions. Next, we will use the information gained from these ex vivo imaging studies to image a small cohort of aged squirrel monkeys in vivo. The brains then will be examined microscopically to identify and characterize the MRI anomalies unambiguously, and to determine the cellular and molecular features of the lesions. We predict that MRI signal anomalies will be linked to specific histopathological indicators of CAA and associated lesions. The findings from this novel primate model will establish a foundation for future non-invasive studies of the pathogenesis, diagnosis and treatment of CAA in aged humans.
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ALZHEIMER'S DISEASE: MODELING PATHOLOGIC STRAIN-LIKE VARIANTS OF MULTIMERIC A?
  • 批准号:
    8357481
  • 项目类别:
  • 资助金额:
    $2.06万
  • 财政年份:
    2011
  • 负责人:
    LARY C WALKER
  • 依托单位:
Cerebral small vessel disease: Enhancing the diagnostic precision of MRI
  • 批准号:
    8226423
  • 项目类别:
  • 资助金额:
    $25.64万
  • 财政年份:
    2011
  • 负责人:
    LARY C WALKER
  • 依托单位:
ALZHEIMER'S DISEASE: MODELING PATHOLOGIC STRAIN-LIKE VARIANTS OF MULTIMERIC A?
  • 批准号:
    8172438
  • 项目类别:
  • 资助金额:
    $2.74万
  • 财政年份:
    2010
  • 负责人:
    LARY C WALKER
  • 依托单位:
ALZHEIMER'S DISEASE: MODELING PATHOLOGIC STRAIN-LIKE VARIANTS OF MULTIMERIC A?
  • 批准号:
    7958265
  • 项目类别:
  • 资助金额:
    $2.75万
  • 财政年份:
    2009
  • 负责人:
    LARY C WALKER
  • 依托单位:
海外基金