Culture-Fair Screening and Diagnosis of Early Dementia

早期痴呆症的文化公平筛查和诊断

基本信息

  • 批准号:
    6545514
  • 负责人:
  • 金额:
    $ 31.67万
  • 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
  • 起止时间:
    2002-09-15 至 2007-08-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): For all patients, the efficacy of new treatments for AD and other dementias may be enhanced when administered during the earliest diagnosable stage of disease. This requires efficient strategies for screening and diagnosing very early dementia at high levels of sensitivity, specificity, and reliability. To achieve this goal in primary care settings, test performance should be minimally influenced by race/ethnicity and education and more sensitive to the memory impairment associated with very early dementia. Our long-term objective is to design efficient culture-fair strategies to identify patients with very early dementia at cross-section for treatment in primary care or for participation in clinical trials. We hypothesize that this will involve rapid screening of all geriatric patients and limited additional testing in patients who screen positive in order to demonstrate memory impairment and another cognitive disturbance as required by DSM IV criteria. A clinical evaluation is triggered only for patients who meet neuropsychological criteria for dementia, making screening and diagnosis feasible in primary care settings. We will also examine the influence of race/ethnicity and education on the diagnostic process. 250 African American and 250 Caucasian patients and their informants will be recruited from an urban geriatric medicine clinic and randomly assigned to 1 of 4 diagnostic conditions defined by whether or not raters know the patient's race and/or education. Diagnosis and clinical staging will be established by consensus at each of 3 waves independent of screening tests and results from other waves. A consensus gold standard diagnosis will be established at the end using the patient's longitudinal record. From the results of this study, we will recommend strategies to maximize the identification of patients with very early dementia at cross section. The specific aims include: Specific Aim 1: To estimate the sensitivity and specificity of each test and test combination for identifying prevalent dementia. Specific Aim 2: To estimate the specificity of each test and test combination at fixed levels of sensitivity for identifying incident dementia. Specific Aim 3: To estimate the effect of knowing race and education on the diagnostic process.
描述(由申请人提供):对于所有患者,在疾病的最早可诊断阶段给予AD和其他痴呆的新治疗方法可能会增强疗效。这就需要高灵敏度、高特异性和高可靠性的早期痴呆筛查和诊断策略。为了在初级保健环境中实现这一目标,测试性能应受种族/民族和教育的影响最小,对与极早期痴呆症相关的记忆障碍更敏感。我们的长期目标是设计有效的文化公平策略,以确定在初级保健治疗或参与临床试验的横截面非常早期痴呆症患者。我们假设,这将涉及快速筛查所有老年患者,并对筛查阳性的患者进行有限的额外检测,以证明记忆障碍和DSM IV标准要求的其他认知障碍。只有符合痴呆症神经心理学标准的患者才能进行临床评估,从而使筛查和诊断在初级保健环境中变得可行。我们还将研究种族/民族和教育对诊断过程的影响。将从城市老年医学诊所招募250名非洲裔美国人和250名白人患者及其知情人,并随机分配至4种诊断条件之一,这些诊断条件由评估者是否了解患者的种族和/或教育程度定义。诊断和临床分期将在3个波中的每一个波通过共识确定,与筛选试验和其他波的结果无关。最终将使用患者的纵向记录建立共识金标准诊断。从这项研究的结果,我们将建议的策略,以最大限度地确定患者的非常早期痴呆症的横截面。具体目标包括:具体目标1:评估每种测试和测试组合识别流行性痴呆的敏感性和特异性。具体目标2:在确定痴呆事件的固定灵敏度水平下,评估每个测试和测试组合的特异性。具体目标3:评估了解种族和教育对诊断过程的影响。

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 }}

Ellen Grober其他文献

Ellen Grober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('Ellen Grober', 18)}}的其他基金

Screening and Diagnosis of Mild Alzheimer's Disease in Latino Elders
拉丁裔老年人轻度阿尔茨海默病的筛查和诊断
  • 批准号:
    8045049
  • 财政年份:
    2011
  • 资助金额:
    $ 31.67万
  • 项目类别:
Screening and Diagnosis of Mild Alzheimer's Disease in Latino Elders
拉丁裔老年人轻度阿尔茨海默病的筛查和诊断
  • 批准号:
    8322005
  • 财政年份:
    2011
  • 资助金额:
    $ 31.67万
  • 项目类别:
Culture-Fair Screening and Diagnosis of Early Dementia
早期痴呆症的文化公平筛查和诊断
  • 批准号:
    6931493
  • 财政年份:
    2002
  • 资助金额:
    $ 31.67万
  • 项目类别:
Culture-Fair Screening and Diagnosis of Early Dementia
早期痴呆症的文化公平筛查和诊断
  • 批准号:
    7100134
  • 财政年份:
    2002
  • 资助金额:
    $ 31.67万
  • 项目类别:
Culture-Fair Screening and Diagnosis of Early Dementia
早期痴呆症的文化公平筛查和诊断
  • 批准号:
    6788796
  • 财政年份:
    2002
  • 资助金额:
    $ 31.67万
  • 项目类别:
Culture-Fair Screening and Diagnosis of Early Dementia
早期痴呆症的文化公平筛查和诊断
  • 批准号:
    6656861
  • 财政年份:
    2002
  • 资助金额:
    $ 31.67万
  • 项目类别:
RACIAL DIFFERENCES IN DEMENTIA SCREENING AND DIAGNOSIS
痴呆症筛查和诊断中的种族差异
  • 批准号:
    6287198
  • 财政年份:
    2001
  • 资助金额:
    $ 31.67万
  • 项目类别:

相似国自然基金

新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
  • 批准号:
    81000622
  • 批准年份:
    2010
  • 资助金额:
    20.0 万元
  • 项目类别:
    青年科学基金项目
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
  • 批准号:
    31060293
  • 批准年份:
    2010
  • 资助金额:
    26.0 万元
  • 项目类别:
    地区科学基金项目
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究
  • 批准号:
    30960334
  • 批准年份:
    2009
  • 资助金额:
    22.0 万元
  • 项目类别:
    地区科学基金项目

相似海外基金

Discovering early biomarkers of Alzheimer's disease using genetic and physics-informed networks
利用遗传和物理信息网络发现阿尔茨海默病的早期生物标志物
  • 批准号:
    2904538
  • 财政年份:
    2024
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Studentship
Deciphering electrophysiological Alzheimer's Disease biomarkers for early diagnosis using interpretable deep learning
使用可解释的深度学习破译电生理阿尔茨海默病生物标志物以进行早期诊断
  • 批准号:
    24K18602
  • 财政年份:
    2024
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
DMS/NIGMS 1: Multilevel stochastic orthogonal subspace transformations for robust machine learning with applications to biomedical data and Alzheimer's disease subtyping
DMS/NIGMS 1:多级随机正交子空间变换,用于稳健的机器学习,应用于生物医学数据和阿尔茨海默病亚型分析
  • 批准号:
    2347698
  • 财政年份:
    2024
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Continuing Grant
Investigating And Targeting Microglial Senescence In Alzheimer's Disease
研究并针对阿尔茨海默病中的小胶质细胞衰老
  • 批准号:
    MR/Y004116/1
  • 财政年份:
    2024
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Research Grant
Histone variant macroH2A1 as a novel regulator of memory deficits in Alzheimer's disease
组蛋白变体 MacroH2A1 作为阿尔茨海默病记忆缺陷的新型调节剂
  • 批准号:
    478226
  • 财政年份:
    2023
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Operating Grants
Incorporating Diversity in Alzheimer's Disease Research: Developing Representative and Generalizable models
将多样性纳入阿尔茨海默病研究:开发代表性和可推广的模型
  • 批准号:
    495662
  • 财政年份:
    2023
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Operating Grants
Development of novel macrocyclic BACE1 inhibitors for preventive or therapeutic agents for Alzheimer's disease
开发用于预防或治疗阿尔茨海默病的新型大环 BACE1 抑制剂
  • 批准号:
    23K06058
  • 财政年份:
    2023
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Fluency from Flesh to Filament: Collation, Representation, and Analysis of Multi-Scale Neuroimaging data to Characterize and Diagnose Alzheimer's Disease
从肉体到细丝的流畅性:多尺度神经影像数据的整理、表示和分析,以表征和诊断阿尔茨海默病
  • 批准号:
    10462257
  • 财政年份:
    2023
  • 资助金额:
    $ 31.67万
  • 项目类别:
Computational modelling of disease progression and subtype discovery in Alzheimer's Disease
阿尔茨海默病疾病进展和亚型发现的计算模型
  • 批准号:
    2885305
  • 财政年份:
    2023
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Studentship
The Contribution of Mitochondrial Dysfunction to Alzheimer's disease
线粒体功能障碍对阿尔茨海默病的影响
  • 批准号:
    2886872
  • 财政年份:
    2023
  • 资助金额:
    $ 31.67万
  • 项目类别:
    Studentship
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了