Neuropathology Core
Neuropathology Core
批准号:
10378617
负责人:
MATTHEW P FROSCH
金额:
$40.41万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-04-15 至 2024-03-31
关键词:
AddressAgingAlzheimer&aposs DiseaseAlzheimer&aposs disease related dementiaAutopsyBiological MarkersBrainCLIA certifiedCell NucleusCellsClassification SchemeClinicalClinical TrialsClinical assessmentsCollaborationsCollectionCommunitiesDataData CollectionDepositionDiagnosisDiagnosticDiseaseDrug or chemical Tissue DistributionEducationEducational ActivitiesEnrollmentEnvironmentFamilyFibroblastsFutureGenerationsGoalsHeterogeneityImageInternationalLiquid substanceMarshalMassachusettsMeasuresMethodologyMethodsMissionNeurodegenerative DisordersNeurologistNurses&apos Health StudyOutcomePathologicPathologic ProcessesPerformancePhasePhysiciansPositioning AttributePublic HealthReportingResearchResearch PersonnelResearch SupportResourcesSamplingScientistSignal TransductionSpecificityStandardizationSystemTimeTissue BanksTissue SampleTissuesTrainingValidationWithdrawalWorkbasebrain tissuecareer developmentcell typeclinical developmentcohortdata sharingdisease heterogeneityexperiencefollow-upinduced pluripotent stem cellinnovationinsightneuropathologynovel strategies
中文摘要
马萨诸塞州阿尔茨海默病研究中心:神经病理学核心
神经病理学核心服务于马萨诸塞州ADRC(MADRC)和阿尔茨海默病研究
社区通过提供临床评估的诊断验证和向研究者提供组织。
神经病理学评估有助于理解AD/ADRD相关的异质性,
无论是在疾病之间还是在并发的病理过程方面。核心组织的可用性
已被研究人员广泛使用,以加速AD/ADRC的治愈。完成这些
我们有三个目标。
第一组(目标1-3)旨在调动资源,重点是收集、诊断、
收集数据,向家属和相关医生全面报告结果,并进行符合CLIA的尸检
报告通过临床核心,并向数据核心的研究目的-和广泛分布的
支持研究社区的样本。异质性问题直接在这些努力中得到解决。
第二组(目标4-6)旨在制定新战略,采用创新方法
为了确定AD/ADRD中影像学和液体生物标志物的神经病理学基础,
AD/ADRD临床试验受试者的神经病理学结果,并从
尸检组织,包括iPSC(将在NCRAD保藏)和分离的细胞类型特异性核。因为这些
三个目标的发展,我们将分享见解,并与其他ADC合作,以验证和广泛的
实施.疾病异质性将在生物标志物基础评估和
信号和临床试验受试者的评估。
最后一组(目标7和8)旨在建设未来,侧重于培训。一是
在AD/ADRD的神经病理学方面培训基础和临床研究人员的组成部分,
组织研究的复杂性和问题。这些工作将与下列机构密切合作进行:
也有努力,与ORE核心合作,在广泛的教育,
尸检和大脑捐赠对加强我们应对AD/ADRD的努力的重要性。
神经病核心与MADRC的所有其他组成部分以及更广泛的科学
社区解决关键问题,以加速治愈AD/ADRD。
英文摘要
Massachusetts Alzheimer’s Disease Research Center: Neuropathology Core
The Neuropathology Core serves both the Massachusetts ADRC (MADRC) and the Alzheimer research
community by providing diagnostic validation of clinical assessments and providing tissue to investigators.
Neuropathologic assessment has contributed to understanding heterogeneity associated with AD/ADRD,
both across diseases and in terms of concurrent pathologic processes. The availability of tissue from the Core
has been widely used by investigators working to accelerate toward a cure for AD/ADRC. To complete these
missions, we have three sets of Aims.
The first group (Aims 1-3), which are intended to marshal resources, is focused on the collection, diagnosis,
collection of data, full reporting of findings – to families and relevant physicians with a CLIA-compliant autopsy
report through the Clinical Core, and to the Data Core for research purposes -- and the wide distribution of
samples in support of the research community. Issues of heterogeneity are directly addressed in these efforts.
The second group (Aims 4-6), which are intended to develop new strategies, incorporate innovate methods
to determine the neuropathologic basis of imaging and fluid biomarkers in AD/ADRD, define the
neuropathologic findings in subjects from clinical trials for AD/ADRD and develop new cellular resources from
autopsy tissue including iPSCs (to be deposited at NCRAD) and isolated cell-type specific nuclei. As these
three aims develop, we will be sharing insights and collaborating with other ADCs for validation and broad
implementation. Disease heterogeneity will be addressed in both the assessment of the basis of biomarker
signals and in the assessment of clinical trials subjects.
The final group (Aims 7 & 8), which are intended to build the future, focus on training. First, there is a
component of training basic and clinical researchers in aspects of the neuropathology of AD/ADRD as well as
the intricacies and issues around tissue-based research. These efforts will be done in close collaboration with
the REC. There are also efforts, done in collaboration with the ORE Core, in broad education about the
importance of autopsy and brain donation to enhance our efforts to tackle AD/ADRD.
The Neuropath Core interacts with all other components of the MADRC and with the broader scientific
community to address critical problems to accelerate towards a cure for AD/ADRD.
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会议论文
Neuropathology Core
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批准号:10620678
-
项目类别:
-
资助金额:$35.37万
-
财政年份:2019
-
负责人:MATTHEW P FROSCH
-
依托单位:
Core D - Neuropathology Core
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批准号:8676353
-
项目类别:
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资助金额:$22.85万
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财政年份:2014
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负责人:MATTHEW P FROSCH
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依托单位:
TRANSGENIC AND KNOCKOUT ANIMAL CORE
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批准号:7483177
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项目类别:
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资助金额:$35.81万
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财政年份:2007
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负责人:MATTHEW P FROSCH
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依托单位:
Spatial and temporal progression of amyloid angiopathy
-
批准号:6789393
-
项目类别:
-
资助金额:$34.6万
-
财政年份:2002
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负责人:MATTHEW P FROSCH
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依托单位:
Spatial and temporal progression of amyloid angiopathy
-
批准号:6934575
-
项目类别:
-
资助金额:$34.6万
-
财政年份:2002
-
负责人:MATTHEW P FROSCH
-
依托单位:
Spatial and Temporal Progression of Amyloid Angiopathy
-
批准号:7844849
-
项目类别:
-
资助金额:$41.8万
-
财政年份:2002
-
负责人:MATTHEW P FROSCH
-
依托单位:
Spatial and Temporal Progression of Amyloid Angiopathy
-
批准号:7477778
-
项目类别:
-
资助金额:$39.8万
-
财政年份:2002
-
负责人:MATTHEW P FROSCH
-
依托单位:
Spatial and Temporal Progression of Amyloid Angiopathy
-
批准号:7320383
-
项目类别:
-
资助金额:$39.43万
-
财政年份:2002
-
负责人:MATTHEW P FROSCH
-
依托单位:
Spatial and Temporal Progression of Amyloid Angiopathy
-
批准号:7617178
-
项目类别:
-
资助金额:$41.0万
-
财政年份:2002
-
负责人:MATTHEW P FROSCH
-
依托单位:
Core--Neuropathology of Parkinson's disease and related Lewy body disorders
-
批准号:6499889
-
项目类别:
-
资助金额:$24.81万
-
财政年份:2001
-
负责人:MATTHEW P FROSCH
-
依托单位:
Core--Neuropathology of Parkinson's disease and related Lewy body disorders
-
批准号:6354788
-
项目类别:
-
资助金额:$24.81万
-
财政年份:2000
-
负责人:MATTHEW P FROSCH
-
依托单位:
CORE--TRANSGENIC ANIMAL
-
批准号:6345909
-
项目类别:
-
资助金额:$22.37万
-
财政年份:2000
-
负责人:MATTHEW P FROSCH
-
依托单位:
Core--Neuropathology of Parkinson's disease and related Lewy body disorders
-
批准号:6341055
-
项目类别:
-
资助金额:$29.46万
-
财政年份:2000
-
负责人:MATTHEW P FROSCH
-
依托单位:
CORE--TRANSGENIC ANIMAL
-
批准号:6201072
-
项目类别:
-
资助金额:$22.37万
-
财政年份:1999
-
负责人:MATTHEW P FROSCH
-
依托单位:
Core--Neuropathology of Parkinson's disease and related Lewy body disorders
-
批准号:6302895
-
项目类别:
-
资助金额:$29.46万
-
财政年份:1999
-
负责人:MATTHEW P FROSCH
-
依托单位:
Core--Neuropathology of Parkinson's disease and related Lewy body disorders
-
批准号:6259569
-
项目类别:
-
资助金额:$29.46万
-
财政年份:1999
-
负责人:MATTHEW P FROSCH
-
依托单位:
CORE--TRANSGENIC ANIMAL
-
批准号:6098805
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项目类别:
-
资助金额:$22.37万
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财政年份:1998
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负责人:MATTHEW P FROSCH
-
依托单位:
Transgenic Animals
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批准号:7468592
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项目类别:
-
资助金额:$13.49万
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财政年份:1998
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负责人:MATTHEW P FROSCH
-
依托单位:
PRESENILIN 1 TRANSGENIC MICE--ALZHEIMER DISEASE MODELS
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批准号:2408471
-
项目类别:
-
资助金额:$6.31万
-
财政年份:1997
-
负责人:MATTHEW P FROSCH
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依托单位:
NOVEL ENDOTHELIAL CELL CADHERIN LIKE MOLECULE
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批准号:2211258
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项目类别:
-
资助金额:$8.69万
-
财政年份:1994
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负责人:MATTHEW P FROSCH
-
依托单位:
海外基金