Epidemiology of Alzheimer's disease resilience and risk pedigrees
Epidemiology of Alzheimer's disease resilience and risk pedigrees
批准号:
10066145
负责人:
John Sai Keong Kauwe
金额:
$7.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-09-01 至 2021-08-31
关键词:
AgeAgingAlzheimer&aposs DiseaseAlzheimer&aposs disease riskAmericanAmyloid beta-ProteinArchivesBloodBody mass indexCardiovascular DiseasesCessation of lifeCognitiveCollectionCommunitiesCountyDNA sequencingDataData AnalysesData CollectionData SetDatabasesDeath CertificatesDepositionDiabetes MellitusDiseaseEnsureEpidemiologic FactorsEpidemiologyEtiologyEuropeanExhibitsFamilyFutureGenealogyGeneticGenetic DiseasesGenotypeGoalsHypertensionImmune responseIn VitroIndividualInflammatory ResponseKnowledgeLinkLongitudinal cohort studyMagnetic Resonance ImagingMalignant NeoplasmsMeasurableMedical RecordsMemoryMutationNatureOdds RatioPhenotypePopulationPopulation DatabasePreventionResearchResourcesRiskRisk FactorsSNP arraySNP genotypingSamplingSeriesSocioeconomic StatusStudy SubjectTestingTherapeutic InterventionUtahVariantWorkapolipoprotein E-4case controlclinical Diagnosiscognitive testingcomputerizeddata submissiondatabase of Genotypes and Phenotypesdensitydesignexome sequencingexperiencegene discoverygenetic analysisgenetic pedigreegenetic risk factorgenetic variantgenome sequencinghealth recordhigh riskinnovationinsightmembermortalitynovelnovel strategiesphenotypic datapopulation basedprecision medicineprotective alleleprotective factorsresiliencetreatment strategytrendwhole genome
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Abstract
Far too many people have personal experience with the destructive nature of
Alzheimer's disease (AD). Despite significant progress identifying genetic risk factors and
increased understanding of the inflammatory and immune response in AD etiology, our
knowledge remains inadequate to develop effective preventions or cures. We have linked data
and subjects from the Utah Population Database (medical records, death certificates, and
genealogy for over 7 million subjects) and the Cache County Study on Memory in Aging
(longitudinal cognitive assessment on over 5,000 subjects in Utah). These samples are an
accurate representation of the general European American population, making findings from
these data generalizable in that context. The combination of these studies enables the
execution of an innovative design for gene discovery, and to evaluate the association between
AD risk and resilience pedigrees, and key aspects of AD epidemiology, including socioeconomic
status, cardiovascular disease, cancer and many others. We will first, conduct studies that
leverage linkage and association to identify novel genetic risk factors. Second, we will use the
UPDB to conduct powerful studies of measurable risk and resilience factors for AD. Third, we
will collect additional samples from key pedigrees to enhance our study. And finally, all data
associated with our effort will be harmonized and deposited into public databases. In summary
our approach is carefully designed and well powered to provide new knowledge and facilitate
efforts to develop a cure for AD. Specifically, we will augment the Cache County Study, an
existing longitudinal cohort study, in an efficient and directed manner, including collecting and
sequencing DNA samples from well-characterized cases and controls in the study. Using our
unparalleled and powerful dataset and approach, we will explore trends in the risk of AD and
their explanation via putative risk and protective factors. Our successful efforts will identify
measurable risk and resilience factors for AD, enabling precision medicine by providing
information for modifying risk in individuals and providing insights into those who will benefit
most from therapeutic interventions. Finally, all data in from this proposal will be harmonized
with relevant datasets and electronically archived in appropriate databases.
期刊论文(7)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1002/trc2.12211
发表时间:
2021
期刊:
Alzheimer's & dementia (New York, N. Y.)
影响因子:
--
作者:
[Dickson SP, Hendrix SB, Brown BL, Ridge PG, Nicodemus-Johnson J, Hardy ML, McKeany AM, Booth SB, Fortna RR, Kauwe JSK, NIAGADS]
通讯作者:
NIAGADS
DOI:
10.1093/nar/gkaa863
发表时间:
2020-11-04
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Hodgman MW, Miller JB, Meurs TE, Kauwe JSK]
通讯作者:
Kauwe JSK
DOI:
10.1038/s41598-020-78803-3
发表时间:
2021-01-12
期刊:
Scientific reports
影响因子:
4.6
作者:
[McKinnon LM, Miller JB, Whiting MF, Kauwe JSK, Ridge PG]
通讯作者:
Ridge PG
Biospecimen Core
-
批准号:10667542
-
项目类别:
-
资助金额:$32.19万
-
财政年份:2021
-
负责人:John Sai Keong Kauwe
-
依托单位:
Biospecimen Core
-
批准号:10172083
-
项目类别:
-
资助金额:$32.84万
-
财政年份:2021
-
负责人:John Sai Keong Kauwe
-
依托单位:
Biospecimen Core
-
批准号:10459240
-
项目类别:
-
资助金额:$32.19万
-
财政年份:2021
-
负责人:John Sai Keong Kauwe
-
依托单位:
Research Supplements to Promote Diversity in Health-Related Research
-
批准号:9114749
-
项目类别:
-
资助金额:$3.46万
-
财政年份:2015
-
负责人:John Sai Keong Kauwe
-
依托单位:
Research Supplements to Promote Diversity in Health-Related Research
-
批准号:9114735
-
项目类别:
-
资助金额:$3.46万
-
财政年份:2015
-
负责人:John Sai Keong Kauwe
-
依托单位:
Pleiotropic and Interaction Effects on Alzheimer's disease Risk and Progression
-
批准号:8791581
-
项目类别:
-
资助金额:$26.64万
-
财政年份:2012
-
负责人:John Sai Keong Kauwe
-
依托单位:
Pleiotropic and Interaction Effects on Alzheimer's disease Risk and Progression
-
批准号:9203039
-
项目类别:
-
资助金额:$25.3万
-
财政年份:2012
-
负责人:John Sai Keong Kauwe
-
依托单位:
Pleiotropic and Interaction Effects on Alzheimer's disease Risk and Progression
-
批准号:9015302
-
项目类别:
-
资助金额:$31.45万
-
财政年份:2012
-
负责人:John Sai Keong Kauwe
-
依托单位:
Pleiotropic and Interaction Effects on Alzheimer's disease Risk and Progression
-
批准号:8344487
-
项目类别:
-
资助金额:$23.77万
-
财政年份:2012
-
负责人:John Sai Keong Kauwe
-
依托单位:
Administrative Supplements to Existing NIH Grants and Cooperative Agreements (Parent Admin Supp)
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批准号:9187245
-
项目类别:
-
资助金额:$9.53万
-
财政年份:2012
-
负责人:John Sai Keong Kauwe
-
依托单位:
海外基金