Subjective Cognitive Complants, Cognitive Decline and B-Amyloid Deposition in Non

非患者的主观认知植入、认知下降和 B 淀粉样蛋白沉积

基本信息

  • 批准号:
    8149860
  • 负责人:
  • 金额:
    $ 10.08万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2010
  • 资助国家:
    美国
  • 起止时间:
    2010-09-30 至 2015-08-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Subjective declines in memory and thinking abilities are commonly reported in older adults. Recent studies indicate that complaints predict subsequent cognitive decline and incident Alzheimer's disease (AD), at least in some older adults. Furthermore, complaints have been associated with biological markers of AD, such as brain atrophy, reduced brain metabolism, and AD neuropathology on autopsy. These findings suggest that, for some, cognitive complaints likely represent a pre-symptomatic stage of AD which may provide an even earlier therapeutic opportunity than mild cognitive impairment (MCI). Amyloid-beta (A¿) imaging studies indicate that brain A¿ plaques are present in 20-30% of cognitively normal older individuals, consistent with postmortem studies. Recent reports show A¿ deposition in normal older adults to be associated with longitudinal cognitive decline, brain volume loss, and altered glucose metabolism, supporting the idea of sub-clinical neuronal dysfunction. The proposed research will investigate whether cognitive complaints may represent a facet of early A¿ -associated, sub-clinical neuronal dysfunction, along with subtle cognitive deficits and gradual cognitive decline. It will also investigate the role of personality, mood and reporting bias in the measurement of subjective cognitive complaints and their relationship to A¿ deposition. This career development proposal will provide the foundation for a research program dedicated to investigating the early natural history of cognition associated with AD pathology in aging. To date, my training has afforded me a broad background in clinical neuropsychology and functional MRI. My short-term goals are to undertake in-depth training in A¿ imaging with PET, using Pittsburgh Compound B (PiB); to learn modern psychometric approaches to develop and refine cognitive outcome scales; and to learn advanced approaches to analyzing longitudinal cognitive data. The institutional environment is well-matched to these training goals, including Mentors Dr. William Klunk, a co-inventor of the amyloid tracer PiB, and Drs. Mary Ganguli and Judith Saxton, each a leader in AD and MCI research. Key elements of the career development plan include supervised research experiences with Mentors/Consultants, courses and workshops. The research plan includes implementation of a complete, original PiB-PET study of cognitively normal participants self-referred to a Memory Disorders Clinic, as well as the step-wise development, refinement and validation of a new scale for subjective cognitive complaints. Through these training and research activities, I will establish myself as an independent scientist with a unique set of skills, utilizing neuroimaging and advances in psychometric measurement to investigate early cognitive predictors of AD. This work will contribute significantly toward understanding the prognostic significance of cognitive complaints and amyloid deposition in non-demented individuals. Potentially, it will advance understanding of the extended preclinical phase of AD and how best to initially identify it. PUBLIC HEALTH RELEVANCE: This research proposal will determine whether subjective complaints of impaired memory and thinking in older adults are related to the pathological brain changes of Alzheimer's disease (AD). It will investigate the role of personality, mood and reporting bias in the measurement of subjective complaints and their relationship to amyloid-beta plaques in the brain. The results could lead to the development of a new scale to initially screen for the presence of very early AD brain changes, potentially leading to improved future treatment outcomes.
描述(由申请人提供):记忆力和思维能力的主观下降通常在老年人中报告。最近的研究表明,至少在一些老年人中,抱怨预示着随后的认知能力下降和阿尔茨海默病(AD)的发生。此外,主诉与AD的生物学标志物相关,如脑萎缩、脑代谢降低和尸检时AD神经病理学。这些研究结果表明,对于一些人来说,认知主诉可能代表AD的症状前阶段,这可能比轻度认知障碍(MCI)提供更早的治疗机会。淀粉样蛋白-β(A ²成像研究表明,大脑A?斑块存在于20-30%的认知正常的老年人中,与死后研究一致。最近的报告显示,在正常老年人中的沉积与纵向认知下降、脑容量损失和葡萄糖代谢改变相关,支持亚临床神经元功能障碍的想法。拟议的研究将调查认知主诉是否可能代表早期A?相关的亚临床神经元功能障碍的一个方面,沿着微妙的认知缺陷和逐渐的认知下降。它还将调查人格,情绪和报告偏见在主观认知投诉的测量及其与A?沉积的关系中的作用。这项职业发展计划将为一项研究计划提供基础,该计划致力于调查与衰老中AD病理学相关的认知早期自然史。到目前为止,我的培训为我提供了临床神经心理学和功能性MRI的广泛背景。我的短期目标是利用匹兹堡化合物B(PiB)进行PET A ²成像的深入培训;学习现代心理测量方法来开发和完善认知结果量表;并学习分析纵向认知数据的先进方法。机构环境与这些培训目标非常匹配,包括导师William Klunk博士,淀粉样蛋白示踪剂PiB的共同发明者,以及玛丽Ganguli和Judith Saxton博士,他们都是AD和MCI研究的领导者。职业发展计划的关键要素包括导师/顾问的监督研究经验、课程和讲习班。该研究计划包括实施一项完整的原始PiB-PET研究,该研究对认知正常的参与者进行自我介绍到记忆障碍诊所,以及逐步开发,改进和验证主观认知投诉的新量表。通过这些培训和研究活动,我将建立自己作为一个独立的科学家与一套独特的技能,利用神经影像学和心理测量的进步,以调查AD的早期认知预测。这项工作将大大有助于了解非痴呆症患者认知障碍和淀粉样蛋白沉积的预后意义。潜在地,它将促进对AD的扩展临床前阶段以及如何最好地最初识别它的理解。 公共卫生关系:这项研究计划将确定老年人记忆和思维受损的主观主诉是否与阿尔茨海默病(AD)的病理性脑变化有关。它将调查人格,情绪和报告偏差在主观抱怨测量中的作用及其与大脑中淀粉样蛋白β斑块的关系。研究结果可能会导致开发一种新的量表,以初步筛选极早期AD大脑变化的存在,从而可能改善未来的治疗结果。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

BETH SNITZ其他文献

BETH SNITZ的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('BETH SNITZ', 18)}}的其他基金

Alzheimer neuroimaging-biomarkers in pre-clinical cognitive decline from a population-based study
基于人群的研究中的阿尔茨海默病神经影像-临床前认知能力下降的生物标志物
  • 批准号:
    9899180
  • 财政年份:
    2016
  • 资助金额:
    $ 10.08万
  • 项目类别:
Alzheimer neuroimaging-biomarkers in pre-clinical cognitive decline from a population-based study
基于人群的研究中的阿尔茨海默病神经影像-临床前认知能力下降的生物标志物
  • 批准号:
    9321764
  • 财政年份:
    2016
  • 资助金额:
    $ 10.08万
  • 项目类别:
Subjective Cognitive Complants, Cognitive Decline and B-Amyloid Deposition in Non
非患者的主观认知植入、认知下降和 B 淀粉样蛋白沉积
  • 批准号:
    8028470
  • 财政年份:
    2010
  • 资助金额:
    $ 10.08万
  • 项目类别:
Cognitive Complaints and Decline and B-Amyloid Deposition in Non-Demented Elderly
非痴呆老年人的认知障碍和衰退以及 B 淀粉样蛋白沉积
  • 批准号:
    8516930
  • 财政年份:
    2010
  • 资助金额:
    $ 10.08万
  • 项目类别:
Cognitive Complaints and Decline and B-Amyloid Deposition in Non-Demented Elderly
非痴呆老年人的认知障碍和衰退以及 B 淀粉样蛋白沉积
  • 批准号:
    8706744
  • 财政年份:
    2010
  • 资助金额:
    $ 10.08万
  • 项目类别:
Cognitive Complaints and Decline and B-Amyloid Deposition in Non-Demented Elderly
非痴呆老年人的认知障碍和衰退以及 B 淀粉样蛋白沉积
  • 批准号:
    8306144
  • 财政年份:
    2010
  • 资助金额:
    $ 10.08万
  • 项目类别:
Clinical Core
临床核心
  • 批准号:
    10410724
  • 财政年份:
    2004
  • 资助金额:
    $ 10.08万
  • 项目类别:
Clinical Core
临床核心
  • 批准号:
    10672908
  • 财政年份:
    2004
  • 资助金额:
    $ 10.08万
  • 项目类别:
Project 1: Amyloid Imaging in Subjective Cognitive Decline
项目 1:淀粉样蛋白成像在主观认知能力下降中的应用
  • 批准号:
    9064038
  • 财政年份:
  • 资助金额:
    $ 10.08万
  • 项目类别:
Clinical Core
临床核心
  • 批准号:
    9927983
  • 财政年份:
  • 资助金额:
    $ 10.08万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了