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Massachusetts Alzheimer's Disease Research Center

Massachusetts Alzheimer's Disease Research Center
马萨诸塞州阿尔茨海默病研究中心
批准号:
10378606
负责人:
BRADLEY T. HYMAN
金额:
$330.67万
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:
Alzheimer&aposs DiseaseAmyloid beta-ProteinAuthorization documentationAutopsyBasic ScienceBehavioralBiological AssayBiological MarkersBloodBlood VesselsCerebrospinal FluidClinicalClinical DataClinical ResearchClinical SciencesClinical TrialsClinical Trials DesignCognitiveCollaborationsCommunitiesDataData LinkagesData SetDementiaDevelopmentDiagnosisDiagnostic ServicesDiseaseEducationEnvironmentEventFacultyFaculty RecruitmentFertilizationFrontotemporal DementiaFunctional disorderFutureGeneral HospitalsGoalsHeterogeneityImageImaging TechniquesImpairmentIndividualInfrastructureInstitutionKnowledgeLaboratoriesLeadershipLearningLesionLewy Body DiseaseLinkMRI ScansMarshalMassachusettsMeasuresMentorsMethodsMissionMolecular ProfilingNatural ImmunityNerve DegenerationNeurofibrillary TanglesNeuropsychologyParticipantPathologyPatientsPhenotypePlasmaPlayPopulation HeterogeneityPositron-Emission TomographyProcessPrognosisResearchResearch MethodologyResearch PersonnelResearch SupportResourcesRoleSamplingScienceScientistStatistical Data InterpretationStructureTechniquesTechnologyTestingTherapeutic TrialsTrainingTraining ProgramsUpdateWorkbasebiomarker validationclinical biomarkersclinical centerclinical phenotypecohortcommunity settingdigitaldisease heterogeneityeducation researchfollow-upfrontotemporal degenerationimaging biomarkerimaging studyinduced pluripotent stem cellinflammatory markerinter-individual variationmedical schoolsmild cognitive impairmentmultidisciplinaryneuroimagingneuropathologynew technologynext generationoutreachpostersprogramsracial and ethnicrecruitresiliencesymposiumtargeted biomarkertau Proteinstherapeutic evaluationtherapeutic targettoolvalidation studies

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英文摘要
OVERVIEW: Massachusetts Alzheimer’s Disease Research Center (MADRC) The MADRC is an interdisciplinary Center at Massachusetts General Hospital, Harvard Medical School, with two major strategic goals: 1) to understand the underpinnings of heterogeneity of Alzheimer’s disease and Alzheimer’s Disease Related Disorders, and 2) to develop techniques, strategies, and technologies to accelerate a cure. To approach these goals, we propose 7 Cores (Administrative, Clinical, Biomarker, Imaging, Neuropathology, Data, and Outreach). We will use advanced Imaging, Biomarker, and analytic approaches to study our Research Cohort, which we view as a state of the art clinical phenotyping laboratory. Autopsy follow up for validation of biomarkers and imaging, and therapeutic targets, is essential. We plan to study a diverse population, both in the sense of various pathophysiologies, and also with varying racial and ethnic backgrounds, and rely on a vigorous ORE core both to fulfill our own recruitment needs and to support clinical trials and other affiliated programs. We have refocused our Center’s activities by remodeling the Research Cohort to include subjects who are cognitively normal, have mild cognitive impairment, or dementia, targeting diverse causes of dementia including Alzheimer’s disease and related disorders (Frontotemporal dementia, Lewy Body Disease, and vascular lesions). We postulate that heterogeneity of progression, even among individuals with the same “disease”, reflects underlying differences that can be uncovered, and that doing so will enhance clinical trial design by parsing variability from the very large, long cohort trials now in common use. Each Core is challenged to develop tools to help accelerate a cure – from intermediate imaging/biomarker targets that may help with diagnosis (a patient’s state) or prognosis (a patient’s fate), to performing autopsies to validate those targets. We will develop markers of inflammation and neurodegeneration, believing that innate immunity and resilience play a role in addition to tangles and plaques. Development of statistical and data methods are critical for anlaysis. These tools will allow us to test hypotheses about faster or slower rates of progression in a deeply phenotyped cohort. A final goal, central to our mission, is to build the future by training the next generation of scientists, which we propose to do under the framework of the Research Education Component. Together, we hope to make a difference in these devastating diseases.
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会议论文
Discovery and development of apoE4 correctors for the treatment of Alzheimer's disease
MGH Diseases of Aging Pathway Via Stimulating Access to Research in Residency (MGH DAP StARR)
  • 批准号:
    10592226
  • 项目类别:
  • 资助金额:
    $26.87万
  • 财政年份:
    2023
  • 负责人:
    BRADLEY T. HYMAN
  • 依托单位:
Multi-omic Brain Cell Atlas of Alzheimer's Disease Progression
LRP1-tau interactions and Alzheimer Disease
  • 批准号:
    10274154
  • 项目类别:
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  • 财政年份:
    2021
  • 负责人:
    BRADLEY T. HYMAN
  • 依托单位:
国内基金
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  • 项目类别:
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  • 资助金额:
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  • 批准年份:
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  • 负责人:
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  • 依托单位:
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  • 批准号:
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  • 项目类别:
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  • 资助金额:
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  • 批准年份:
    2010
  • 负责人:
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  • 依托单位:
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