UK-ADRC neuroimaging supplement: LATE and PART
UK-ADRC neuroimaging supplement: LATE and PART
批准号:
10170755
负责人:
BRIAN Timothy GOLD
金额:
$36.72万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-07-15 至 2023-06-30
关键词:
AddressAfrican AmericanAlzheimer&aposs DiseaseAlzheimer&aposs disease related dementiaAmyloidAutopsyBiologicalBiological MarkersBiometryBrainBrain imagingCerebrovascular DisordersCessation of lifeCharacteristicsClinicalClinical TrialsClinical assessmentsCognitiveCognitive agingCollectionCommunitiesDataData SetDegenerative DisorderDementiaDevelopmentDiseaseEducationEducation and OutreachElderlyEnvironmentFosteringFundingGeneticGoalsHigh PrevalenceImageImpairmentIndividualInfrastructureKentuckyLettersLiquid substanceLongitudinal cohortMagnetic Resonance ImagingMissionNatureParticipantPathogenicityPathologicPathologyPatternPhenotypeProtocols documentationResearchResearch PersonnelResourcesScanningSpectrum AnalysisStandardizationTauopathiesTimeTranslationsUnited StatesUnited States National Institutes of HealthUniversitiesage relatedagedaging populationbasebiomarker developmentbiomarker discoverycentral databaseclinical developmentclinical phenotypecohortdata managementeducation researchexperiencehippocampal atrophyhuman old age (65+)in vivoinnovationknowledge translationlimbic-predominant age-related TDP-43 encephalopathylongitudinal analysismachine learning algorithmneurochemistryneuroimagingneuroimaging markerneuropathologynew therapeutic targetnormal agingnovel markernovel therapeuticsoutreachparent grantpre-clinicalpreclinical studyprogramsrecruitresearch studystatisticssuccesstau Proteinsvascular cognitive impairment and dementiawhite matter
中文摘要
项目摘要/摘要-总体(改编自《家长赠款摘要》,英国-ADC)
这是肯塔基大学阿尔茨海默病研究中心(UK-ADRC)的一份提案
神经影像补充剂。该附录的目的是提供英国-ADRC的神经成像数据
NIH最近资助的标准化集中式阿尔茨海默氏症的深度表型临床队列
及相关痴呆症的神经影像(扫描)。此外,本补编的次要目的是
确定两个AD模拟物的神经影像相关性:边缘为主的年龄相关性TDP-43脑病
(晚期)和原发年龄相关的肌张力障碍(部分)。英国-ADRC是一个经验丰富和合作的ADRC
最初是在1985年资助的。我们的主要使命是成为英国所有与AD相关的活动的联络人
以及美国的这一地区,通过提供一个环境和核心资源来催化创新
研究、推广、教育和临床项目。我们的标志性资源包括:1)认知正常
一组约500名受试者进行了纵向跟踪,所有人都在死亡时进行了脑部尸检;2)强大的
临床-神经病理相关性和短时间尸检计划;3)建立
使用神经影像和生物体液研究AD的临床前生物标记物的计划;4)集成的集中式
数据库和创新的生物统计学专门知识,以确定临床和生物转变的特征;以及5)a)
与非洲裔美国人社区建立了成功和密切的伙伴关系,并增加了
在我们的纵向队列和ADRC附属研究和临床试验中,代表不足的个人。
英国-ADRC的总体科学重点继续放在我们相互关联的主题上:过渡和
翻译。我们的特点良好的纵向队列和历史上强大的神经病理学计划
关注正常衰老、临床前疾病状态和早期认知转变一直是我们
成功地确定了从正常认知老化到
减损。我们调查人员的深度专业知识和合作性质也导致了
在将这一知识转化为新的靶点和新的治疗策略方面取得了实质性进展。这个
英国-ADRC提供了一个专注于这些综合主题和进展的基础设施和环境
通过高度互动和有效的组件开展广告研究、教育、推广和临床计划:
行政核心、临床核心、数据管理和统计核心、神经病理学核心、外展和
招聘核心、生物标记核心和研究教育部分。英国-ADRC将提供资源
从这些可用的核心支持ADRC神经成像补充的成功。
英文摘要
PROJECT SUMMARY/ABSTRACT – OVERALL (Adapted from Abstract of parent grant, UK-ADC)
This is a proposal for a University of Kentucky Alzheimer’s Disease Research Center (UK-ADRC)
neuroimaging supplement. This purpose of the supplement is to provide neuroimaging data on the UK-ADRC’s
deeply phenotyped clinical cohort to the NIH’s recently funded initiative, Standardized Centralized Alzheimer's
and Related Dementias Neuroimaging (SCAN). In addition, a secondary purpose of this supplement is to
identify neuroimaging correlates of two AD-mimics: limbic-predominant age-related TDP-43 encephalopathy
(LATE) and primary age-related tauopathy (PART). The UK-ADRC is an experienced and collaborative ADRC
originally funded in 1985. Our principal mission is to serve as the focal point for all AD-related activities at UK
and this region of the United States, by providing an environment and core resources that catalyze innovative
research, outreach, education, and clinical programs. Our signature resources include: 1) a cognitively normal
group of ~500 subjects followed longitudinally, with all committed to brain autopsy upon death; 2) a strong
program in clinical-neuropathological correlations and short postmortem interval autopsies; 3) an established
program studying preclinical biomarkers of AD using neuroimaging and biofluids; 4) an integrated centralized
database and innovative biostatistical expertise to characterize clinical and biological transitions; and 5) a
successful and close partnership with the African-American community and increased participation of
underrepresented individuals in our longitudinal cohort and ADRC-affiliated research studies and clinical trials.
The overall scientific emphasis of the UK-ADRC continues to be on our interrelated themes: Transitions &
Translation. Our well-characterized, longitudinal cohort and historically strong neuropathology program
focused on normal aging, preclinical disease states and early cognitive transitions have been central to our
success in defining early pathogenic mechanisms underlying the transitions from normal cognitive aging to
impairment. The depth of expertise and collaborative nature of our investigators have also resulted in
substantial progress on translation of that knowledge into new targets and novel therapeutic strategies. The
UK-ADRC provides an infrastructure and environment that focuses on these integrated themes and advances
AD research, education, outreach, and clinical programs through highly interactive and effective components:
Administrative Core, Clinical Core, Data Management and Statistics Core, Neuropathology Core, Outreach and
Recruitment Core, Biomarker Core, and Research Education Component. The UK-ADRC will make resources
from these Cores available to support the success of this ADRC neuroimaging supplement.
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DOI:
10.1002/hbm.23494
发表时间:
2017-04
期刊:
Human brain mapping
影响因子:
4.8
作者:
[Mullins RJ, Mustapic M, Goetzl EJ, Kapogiannis D]
通讯作者:
Kapogiannis D
DOI:
10.1177/23337214211068290
发表时间:
2022-01
期刊:
Gerontology & geriatric medicine
影响因子:
2.7
作者:
[Rhodus EK, Hunter EG, Rowles GD, Bardach SH, Parsons K, Barber J, Thompson M, Jicha GA]
通讯作者:
Jicha GA
DOI:
10.1016/j.cortex.2018.04.006
发表时间:
2018-07
期刊:
Cortex; a journal devoted to the study of the nervous system and behavior
影响因子:
--
作者:
[Brown CA, Jiang Y, Smith CD, Gold BT]
通讯作者:
Gold BT
DOI:
10.1097/wad.0000000000000425
发表时间:
2021-04-01
期刊:
Alzheimer disease and associated disorders
影响因子:
2.1
作者:
[Bardach SH, Langbaum JB, Kebodeaux CS, Jicha GA]
通讯作者:
Jicha GA
DOI:
10.3389/fnagi.2016.00015
发表时间:
2016
期刊:
Frontiers in aging neuroscience
影响因子:
4.8
作者:
[Jiang Y, Huang H, Abner E, Broster LS, Jicha GA, Schmitt FA, Kryscio R, Andersen A, Powell D, Van Eldik L, Gold BT, Nelson PT, Smith C, Ding M]
通讯作者:
Ding M
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