Integrative Network Modeling of Cognitive Resilience to Alzheimer's Disease
Integrative Network Modeling of Cognitive Resilience to Alzheimer's Disease
批准号:
9439453
负责人:
MICHELLE E EHRLICH
金额:
$132.28万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-15 至 2022-05-31
关键词:
Academic Medical CentersActivities of Daily LivingAffectAgeAgingAlzheimer&aposs DiseaseAlzheimer&aposs disease modelAlzheimer&aposs disease riskAutopsyBiological ModelsBiologyBrainCaenorhabditis elegansCategoriesCessation of lifeClinicalClinical DataCognitiveDNA sequencingDataData SetDementiaDeteriorationDevelopmentDiseaseElderlyGene ProteinsGenesGeneticGenotype-Tissue Expression ProjectGoalsHumanImmunocompetenceIndividualLeadMapsMeasurableMemoryMemory LossMessenger RNAMethodsMitochondriaMolecularMolecular ProfilingNeurodegenerative DisordersNeurofibrillary TanglesPathologicPatientsPersonsPopulationPrefrontal CortexPrevention strategyProteinsProteomicsResearchRisk FactorsScientistSenile PlaquesSignal PathwayStructureSystemTestingTissue SampleVariantaging brainbrain tissuecohortcombatdata modelingdifferential expressionepigenetic markergenetic varianthigh dimensionalityin vivo Modelmedical schoolsmolecular scalemouse modelnetwork modelsnon-dementednovelpreventresiliencetranscriptomics
中文摘要
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英文摘要
Project Summary
Alzheimer's disease (AD) is a debilitating neurodegenerative disorder. Pathologically, AD is characterized by
amyloid plaques and neurofibrillary tangles. Clinically, AD patients present with progressive memory decline
followed by deterioration of other cognitive domains and activities of daily living. Advanced age is the greatest
risk factor. No effective method is available for preventing and/or treating this devastating disease. However,
certain individuals of the elder population (≥ 85 years) remain cognitively intact, including some with substantial
plaques and neurofibrillary tangle burdens, the two pathological hallmarks for fully symptomatic AD. The
mechanisms of cognitive resilience and protection against AD in these elderly persons remain elusive. This
proposal brings together scientists and postmortem human brain tissue samples from two major AD-research
centers (the Icahn School of Medicine at Mount Sinai and the Rush University Medical Center) and aims to
systematically identify and validate genetic variants, genes, proteins, and molecular networks underlying
cognitive resilience to AD risk and proposes to build a comprehensive unbiased signaling pathway map
underlying cognitive resilience to AD. Towards this end, we will develop an AD resilient cohort comprised of
genetic, transcriptomic and proteomic data in the prefrontal cortex from a large number of brains in four
categories: 1) very old (age of death (AoD) ≥ 85) AD-resilient, 2) young (AoD < 85) healthy, 3) very old (AoD
≥85) AD and 4) young (AoD < 85) AD. We will perform systems genetics and integrative network biology
analyses on the large-scale high-dimensional molecular profiling data to identify genetic variants, genes,
proteins, and molecular networks underlying cognitive resilience to AD risk. We will systematically validate key
drivers of the molecular networks underlying the cognitive resilience to AD using two diverse (C. elegans and
mouse) model systems. We will validate the structures of AD-resilient molecular networks for building a data-
driven, comprehensive signaling pathway map underlying cognitive resilience to AD risk. In particular, we will
test the hypotheses that enhanced mitochondrial function and immune competence as well as their underlying
molecular networks confer cognitive resilience. Our study will not only present a global landscape of the
interplays among genetic variants, mRNAs and proteins responsible for cognitive resilience to AD but also
pinpoint critical network structures and key drivers that can potentially lead to development of novel prevention
strategies in combating AD.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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依托单位:
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依托单位:
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依托单位:
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项目类别:
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资助金额:$227.24万
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依托单位:
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财政年份:2014
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依托单位:
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依托单位:
Dopamine D1 Receptor in mouse models of primary dystonia
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财政年份:2013
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负责人:MICHELLE E EHRLICH
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依托单位:
Dopamine D1 Receptor in mouse models of primary dystonia
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项目类别:
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资助金额:$50.12万
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财政年份:2013
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Integrative Biology Approach to Complexity of Alzheimer's Disease
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批准号:9411217
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资助金额:$16.95万
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财政年份:2013
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依托单位:
Integrative Network Biology Approaches to Identify, Characterize and Validate Molecular Subtypes in Alzheimer's Disease
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Huntington's Disease and the Striatum
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依托单位:
海外基金