1Florida Alzheimer's Disease Research Center Biomarker Core
1佛罗里达阿尔茨海默病研究中心生物标志物核心
基本信息
- 批准号:10190777
- 负责人:
- 金额:$ 27.62万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-06-15 至 2025-04-30
- 项目状态:未结题
- 来源:
- 关键词:African AmericanAlzheimer&aposs DiseaseAlzheimer&aposs disease diagnosisAmyloidAmyloid beta-ProteinAmyloid depositionAutopsyBackBiologicalBiological AssayBiological MarkersCharacteristicsClassification SchemeClinicalClinical DataCognitive agingCommunicationDataData SetDatabasesDementiaDiffusionDisease ProgressionEducationElderlyFloridaFundingFutureGoalsGoldGrantHippocampus (Brain)Hispanic AmericansImageIndividualInfrastructureLightMachine LearningMagnetic Resonance ImagingMeasuresMemory DisordersMissionModalityMultimodal ImagingNerve DegenerationNeuritesOnline SystemsParticipantPathologyPathway interactionsPlasmaPositron-Emission TomographyProcessProtocols documentationProxyPublishingResearchResearch PersonnelResearch TrainingSiteStructureTimeUniversitiesWaterWorkbasecognitive neurosciencecohortcomputational platformcomputerized data processingdata managementdata sharingdeep learningdemographicsdensityhealthy agingimage processingimaging modalityin vivoinnovationmachine learning algorithmmultimodal datamultimodalityneurofilamentneuroimagingnovelsoftware developmentspecific biomarkerssupport vector machinetau Proteinstractographyweb serviceswhite matterβ-amyloid burden
项目摘要
SUMMARY: Biomarker Core
Alzheimer’s disease (AD) classically develops in the elderly. The classical way to confirm an AD diagnosis is the
presence of amyloid deposition and tau pathology at post-mortem; however in-vivo biomarkers can serve as
proxies of these characteristics and are invaluable in separating healthy aging from AD as well as placing
individuals along the AD continuum. The Biomarker Core works closely with the three Clinical Core sites across
Miami and Gainesville, as well as the Data Core to provide timely access to raw, pre-processed, and post-
processed data. The Aims of this Biomarker Core include: 1) Web-based Neuroimaging Portal for Accessing,
Visualizing, and Sharing Multimodal Imaging Data. 2) Integrating New Imaging and Biofluid Modalities into the
Neuroimaging Portal. 3) Multimodal, Multiclass, and Machine Learning Algorithms of Imaging and Biofluid
Markers. 4) Provide Support for Ongoing and Future R01, U01, REC, K01, K99, T32, and F32 grants across the
network of Florida and non-Florida Projects. There is a rich and expansive group of grants that will be able to
leverage the biomarker datasets acquired within the Clinical Core, including those funded as part of the Research
and Education Core (REC). This core will provide the needed communication, data sharing, analysis support,
and neuroimaging training for research in these projects to proceed. We believe that this study, which would be
one of the largest of its kind, will combine data acquired at the Wien Center for Alzheimer’s Disease and Memory
Disorders, UM Center for Cognitive Neuroscience and Aging, and University of Florida. Access to this new
multimodal dataset in AD and other dementias will provide added statistical meaningfulness in studying dementia
and inclusion of a large number of Hispanics and African Americans, which is much needed given the current
demographics of the popular ADNI database.
摘要:生物标志物核心
阿尔茨海默氏病(AD)经典地在古老的角度发展。确认AD诊断的经典方法是
验尸后存在淀粉样蛋白沉积和tau病理学;但是,体内生物标志物可以作为
这些特征的代表,在将健康的衰老与AD分开以及放置方面是无价的
沿广告连续体的个人。生物标志物核心与三个临床核心部位紧密合作
迈阿密和盖恩斯维尔以及数据核心,可及时访问原始,预处理和后
处理的数据。该生物标志物核心的目的包括:1)基于Web的神经成像门户用于访问,
可视化和共享多模式成像数据。 2)将新的成像和生物流体方式整合到
神经影像门户。 3)成像和生物流体的多模式,多类和机器学习算法
标记。 4)为正在进行和未来的R01,U01,REC,K01,K99,T32和F32的支持提供支持
佛罗里达州和非氯化氯化氯化绿色项目的网络。有一群丰富而广泛的赠款能够
利用临床核心内获得的生物标志物数据集,包括作为研究的一部分资助的生物标志物
和教育核心(REC)。该核心将提供所需的通信,数据共享,分析支持,
以及在这些项目中进行研究的神经影像学培训。我们认为这项研究将是
同类中最大的是,将在阿尔茨海默氏病和记忆中心中获得的数据结合
疾病,UM认知神经科学与衰老中心以及佛罗里达大学。访问这个新的
AD和其他痴呆症中的多模式数据集将在研究痴呆症时提供额外的统计意义
以及包括大量西班牙裔和非洲裔美国人,鉴于当前
流行的ADNI数据库的人口统计。
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)
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David E Vaillancourt其他文献
Evaluating Spatial Filtering on Diffusion MRI Data Harmonization in Parkinsonism
评估帕金森病扩散 MRI 数据协调的空间过滤
- DOI:
10.32473/ufjur.24.130754 - 发表时间:
2022 - 期刊:
- 影响因子:0
- 作者:
Madelyn Corliss;David E Vaillancourt - 通讯作者:
David E Vaillancourt
Aducanumab reduces Aβ plaques in Alzheimer's disease
- DOI:
10.1002/mds.26833 - 发表时间:
2016-11 - 期刊:
- 影响因子:8.6
- 作者:
David E Vaillancourt - 通讯作者:
David E Vaillancourt
David E Vaillancourt的其他文献
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{{ truncateString('David E Vaillancourt', 18)}}的其他基金
Automated Imaging Differentiation of Parkinsonism
帕金森病的自动成像鉴别
- 批准号:
10613607 - 财政年份:2022
- 资助金额:
$ 27.62万 - 项目类别:
1Florida Alzheimer's Disease Research Center Biomarker Core
1佛罗里达阿尔茨海默病研究中心生物标志物核心
- 批准号:
10663246 - 财政年份:2020
- 资助金额:
$ 27.62万 - 项目类别:
1Florida Alzheimer's Disease Research Center Biomarker Core
1佛罗里达阿尔茨海默病研究中心生物标志物核心
- 批准号:
10413196 - 财政年份:2020
- 资助金额:
$ 27.62万 - 项目类别:
1Florida Alzheimer's Disease Research Center Biomarker Core
1佛罗里达阿尔茨海默病研究中心生物标志物核心
- 批准号:
9921607 - 财政年份:2020
- 资助金额:
$ 27.62万 - 项目类别:
Non-invasive Markers of Neurodegeneration in Movement Disorders
运动障碍神经退行性变的非侵入性标志物
- 批准号:
8643868 - 财政年份:2012
- 资助金额:
$ 27.62万 - 项目类别:
Non-invasive Markers of Neurodegeneration in Movement Disorders
运动障碍神经退行性变的非侵入性标志物
- 批准号:
8661314 - 财政年份:2012
- 资助金额:
$ 27.62万 - 项目类别:
Non-invasive Markers of Neurodegeneration in Movement Disorders
运动障碍神经退行性变的非侵入性标志物
- 批准号:
8550151 - 财政年份:2012
- 资助金额:
$ 27.62万 - 项目类别:
Non-invasive Markers of Neurodegeneration in Movement Disorders
运动障碍神经退行性变的非侵入性标志物
- 批准号:
9068252 - 财政年份:2012
- 资助金额:
$ 27.62万 - 项目类别:
Non-invasive Markers of Neurodegeneration in Movement Disorders
运动障碍神经退行性变的非侵入性标志物
- 批准号:
8875784 - 财政年份:2012
- 资助金额:
$ 27.62万 - 项目类别:
Non-invasive Markers of Neurodegeneration in Movement Disorders
运动障碍神经退行性变的非侵入性标志物
- 批准号:
8366809 - 财政年份:2012
- 资助金额:
$ 27.62万 - 项目类别:
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