Michigan Alzheimer's Disease Research Center
密歇根阿尔茨海默病研究中心
基本信息
- 批准号:10473806
- 负责人:
- 金额:$ 307.59万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-09-01 至 2026-06-30
- 项目状态:未结题
- 来源:
- 关键词:AddressAffectAfrican AmericanAgingAlzheimer&aposs DiseaseAlzheimer&aposs disease related dementiaAlzheimer&aposs disease therapyAmericanAmyloid beta-ProteinAwardBiological MarkersBlack AmericanBlack raceCapsicumCenters of Research ExcellenceClinicalCognitionCollaborationsCommunitiesDementiaDevelopmentDiagnosisDiagnosticDisclosureDiseaseEducation and OutreachElderlyEnsureEnvironmentFoundationsFundingHealthHealth Disparities ResearchHealth ProfessionalHeterogeneityHispanicKnowledgeLatinoLeadLewy Body DementiaLightLinkLongitudinal cohortMentorsMichiganModificationMolecular ProfilingMulti-Institutional Clinical TrialNerve DegenerationNonpharmacologic TherapyParkinson DiseaseParticipantPeripheralPopulation ResearchProtein-Folding DiseaseResearchResearch SubjectsResearch SupportResourcesRiskScientistSiteStudentsTherapeuticTrainingUnited StatesUniversitiesVascular DementiaWorkaging demographybrain dysfunctioncontextual factorsdisorder riskeducation researchexperiencefrontotemporal lobar dementia-amyotrophic lateral sclerosisgene environment interactionhealth disparityimprovedinnovationmolecular imagingneuroimaging markernext generationnovelnovel diagnosticsnovel markernovel therapeutic interventionoutreachprogramsracial diversityrecruitsymposiumtraining opportunitytranslational neuroscience
项目摘要
ABSTRACT – OVERALL
Four years ago the Michigan ADRC (MADRC) was established as a new consortium linking the three major
research universities in Michigan: University of Michigan, Michigan State University, and Wayne State
University. Serving the entire state of Michigan, the new MADRC achieved its milestones in wide-ranging
activities and research that emphasized a central theme: to identify, understand and treat the myriad non-β-
amyloid contributions to brain dysfunction and degeneration in Alzheimer’s disease and related dementias
(ADRD). With continued NIA support, the MADRC proposes to maintain this central theme because it captures
the diverse expertise of our dementia scientists, sheds light on ADRD heterogeneity, and reflects the
experience of the racially diverse pool of research participants engaged in MADRC-sponsored studies. To
achieve its objectives, the MADRC has four major aims: 1) Catalyze and perform research of the highest
impact in ADRD; 2) Promote regional efforts to understand, diagnose and treat the full spectrum of dementias
through collaborative scientific and outreach efforts; 3) Provide training and research opportunities for health
care professionals, scientists, and students in ADRD through innovative educational and mentoring programs;
and 4) Collaborate with other ADRCs, the NACC, NCRAD, and other multi-center efforts to lead the field in
developing new diagnostic and therapeutic interventions for these devastating diseases. The integrated efforts
of seven Cores, including new Neuroimaging and Biomarker cores, will support a wide range of basic, clinical,
translational and health disparities research advancing the field toward: improved understanding of disease
mechanisms; more precise disease identification across the dementia spectrum; development of novel
biomarkers; increased knowledge of the basis for health disparities that disproportionately affect Black
Americans; development of non-pharmacological therapies; and the identification and modification of disease
risks. The Research Education Component (REC) will serve as the centerpiece of innovative training
opportunities spanning all the Cores, and a new Leaders Initiative will support and promote a diverse group of
next-generation leaders in dementia research. Benefitting from the outstanding resources of all three
universities and strong multi-institutional support, the MADRC is poised to make new discoveries, educate the
public, and train next-generation leaders as we seek to achieve the milestones set forth in the National
Alzheimer’s Project Act.
摘要-总体
四年前,密歇根州ADRC(MADRC)成立,作为一个新的财团连接三大
密歇根州的研究型大学:密歇根大学、密歇根州立大学和韦恩州立大学
大学新的MADRC服务于整个密歇根州,在广泛的领域取得了里程碑式的成就。
活动和研究,强调一个中心主题:识别,理解和治疗无数的非β-
淀粉样蛋白在阿尔茨海默病和相关痴呆中对脑功能障碍和变性的作用
(ADRD).在NIA的持续支持下,MADRC建议保持这一中心主题,因为它抓住了
我们的痴呆症科学家的不同专业知识,揭示了ADRD的异质性,并反映了
参与MADRC赞助研究的不同种族研究参与者的经验。到
为了实现其目标,MADRC有四个主要目标:1)催化和执行最高水平的研究
2)促进区域努力,以了解、诊断和治疗各种痴呆症
通过协作性的科学和外联努力; 3)提供卫生培训和研究机会
通过创新的教育和指导计划,护理专业人员,科学家和ADRD学生;
4)与其他ADRC、NACC、NCRAD和其他多中心努力合作,在以下方面引领该领域:
为这些毁灭性疾病开发新的诊断和治疗干预措施。的综合努力
七个核心,包括新的神经影像和生物标志物核心,将支持广泛的基础,临床,
翻译和健康差异研究推进该领域朝着:提高对疾病的理解
机制;更精确的疾病识别整个痴呆症谱;开发新的
生物标志物;增加对不成比例地影响黑人的健康差异的基础的了解
美国人;非药物治疗的发展;以及疾病的识别和改变
风险研究教育部分(REC)将作为创新培训的核心
机会跨越所有的核心,一个新的领导人倡议将支持和促进一个多元化的群体,
痴呆症研究的下一代领导者。得益于这三家公司的优秀资源
大学和强大的多机构支持,MADRC准备作出新的发现,教育
公众,并培养下一代领导人,因为我们寻求实现国家
老年痴呆症项目法案
项目成果
期刊论文数量(0)
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Henry L Paulson其他文献
Technology Insight: therapeutic RNA interference—how far from the neurology clinic?
技术洞察:治疗性 RNA 干扰——距离神经学临床还有多远?
- DOI:
10.1038/ncpneuro0551 - 发表时间:
2007-07-01 - 期刊:
- 影响因子:33.100
- 作者:
Pedro Gonzalez-Alegre;Henry L Paulson - 通讯作者:
Henry L Paulson
Henry L Paulson的其他文献
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{{ truncateString('Henry L Paulson', 18)}}的其他基金
Michigan Alzheimer’s Disease Research Center-Supplement
密歇根阿尔茨海默病研究中心增刊
- 批准号:
10599387 - 财政年份:2021
- 资助金额:
$ 307.59万 - 项目类别:
Mechanisms of neurodegenerative diseases: intersections with ubiquitin pathways
神经退行性疾病的机制:与泛素通路的交叉
- 批准号:
10396120 - 财政年份:2021
- 资助金额:
$ 307.59万 - 项目类别:
Mechanisms of neurodegenerative diseases: intersections with ubiquitin pathways
神经退行性疾病的机制:与泛素通路的交叉
- 批准号:
10619544 - 财政年份:2021
- 资助金额:
$ 307.59万 - 项目类别:
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