grant

Racial Differences in Late-Life Cognitive decline and risk of Alzheimer's Disease

Organization RUSH UNIVERSITY MEDICAL CENTERLocation CHICAGO, UNITED STATESPosted 30 Sept 2004Deadline 31 May 2027
NIHUS FederalResearch GrantFY202521+ years oldAD dementiaAD preventionASCVDActive Follow-upAddressAdultAdult HumanAfrican AmericanAfro AmericanAfroamericanAgingAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer disease preventionAlzheimer preventionAlzheimer risk factorAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimer's disease riskAlzheimers DementiaAmentiaArteriolosclerosesAtherosclerosisAtherosclerotic Cardiovascular DiseaseAutopsyAwarenessBehaviorBiologicalBlackBlack PopulationsBlack groupBlack individualBlack peopleBlack raceBlacksBloodBlood PlasmaBlood Reticuloendothelial SystemBlood VesselsBrainBrain Nervous SystemCOVID crisisCOVID epidemicCOVID pandemicCOVID-19COVID-19 affectedCOVID-19 consequenceCOVID-19 crisisCOVID-19 effectCOVID-19 epidemicCOVID-19 eraCOVID-19 global health crisisCOVID-19 global pandemicCOVID-19 health crisisCOVID-19 impactCOVID-19 impactedCOVID-19 pandemicCOVID-19 periodCOVID-19 public health crisisCOVID-19 yearsCV-19Cardiovascular DiseasesCerebral Amyloid AngiopathyChronicClinicalCognitionCognitiveCognitive DiscriminationCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalCohort StudiesConcurrent StudiesCongophilic AngiopathyCoronavirus Infectious Disease 2019CoupledDataData CollectionDecrease disparityDementiaDiscriminationDiseaseDisorderDisparitiesDisparityDisturbance in cognitionEducationEducational aspectsEncephalonEpidemiologyEthnic GroupEthnic PeopleEthnic PopulationEthnic individualEthnicity PeopleEthnicity PopulationFundingGoalsHealthHealth Care UtilizationHortega cellImpaired cognitionIndividualInequityInfarctionInflammationInflammatoryInterventionInvestigationKnowledgeLeadLinkLived experienceLived experiencesLower disparityMeasuresMedicare claimMemoryMental HealthMental HygieneMicrogliaMinorityNeighborhoodsNeurobiologyOlder PopulationParticipantPathologicPathologyPathway interactionsPatternPb elementPersonsPhysical activityPlasmaPlasma SerumPoliciesPopulationPreventionPrimary Senile Degenerative DementiaProteinsProteomicsProtocolProtocols documentationPsychological HealthPsychological ImpactRaceRacesRacial GroupReproducibilityResearchResearch ResourcesResourcesReticuloendothelial System, Serum, PlasmaRisk FactorsSARS-CoV-2 epidemicSARS-CoV-2 global health crisisSARS-CoV-2 global pandemicSARS-CoV-2 pandemicSARS-coronavirus-2 epidemicSARS-coronavirus-2 pandemicSample SizeSevere Acute Respiratory Syndrome CoV 2 epidemicSevere Acute Respiratory Syndrome CoV 2 pandemicSevere acute respiratory syndrome coronavirus 2 epidemicSevere acute respiratory syndrome coronavirus 2 pandemicSocial ImpactsSocietiesSourceStressStructural RacismSystemTestingTherapeuticViolenceaccess to health careaccessibility of health careaccessibility to health careactive followupadulthoodaged groupaged groupsaged individualaged individualsaged peopleaged personaged personsaged populationaged populationsaging populationalzheimer riskatheromatosisatherosclerotic diseaseatherosclerotic vascular diseasebiologicbrain healthbrain tissuebrain vascular pathologybrain vascular pathophysiologycardiovascular disordercerebral angiopathycerebral vascular pathologycerebral vasculopathycerebrovascular abnormalitycerebrovascular amyloidosiscerebrovascular defectcerebrovascular disease pathologycerebrovascular pathologycerebrovascular pathophysiologycerebrovasculopathycognitive dysfunctioncognitive losscohortcoronavirus disease 2019coronavirus disease 2019 consequencecoronavirus disease 2019 crisiscoronavirus disease 2019 effectcoronavirus disease 2019 epidemiccoronavirus disease 2019 global health crisiscoronavirus disease 2019 global pandemiccoronavirus disease 2019 health crisiscoronavirus disease 2019 impactcoronavirus disease 2019 pandemiccoronavirus disease 2019 public health crisiscoronavirus disease crisiscoronavirus disease epidemiccoronavirus disease pandemiccoronavirus disease-19coronavirus disease-19 global pandemiccoronavirus disease-19 impactcoronavirus disease-19 pandemiccoronavirus infectious disease-19dementia burdendementia riskdensitydifferences due to racedifferences in racediffers by racediffers in racedisparities in racedisparity due to racedisparity in healthdisparity reductionepidemiologicepidemiologicalethnic subgroupethnicity groupfollow upfollow-upfollowed upfollowupgitter cellhealth care accesshealth care availabilityhealth care service accesshealth care service availabilityhealth care service usehealth care service utilizationhealth disparityheavy metal Pbheavy metal leadhospitalization ratesinequality due to raceinequity due to raceinfarctlate in lifelate lifemesogliamicroglial cellmicrogliocytemitigate disparitynecropsyneurobiologicalneuropathologicneuropathologicalneuropathologynovelolder groupsolder individualsolder personpandemicpandemic diseasepathwayperivascular glial cellphysical conditioningphysical healthpoor health outcomepopulation agingpostmortemprimary degenerative dementiapublic health prioritiesrace based differencesrace based disparityrace based inequalityrace based inequityrace differencesrace disparityrace related differencesrace related disparityrace related inequalityrace related inequityracialracial backgroundracial differenceracial disparityracial inequalityracial inequityracial originracial populationracial subgroupracially differentracially unequalreduce disparityreduced health outcomereduction in disparityresearch studyresidential segregationrisk factor for dementiarisk for dementiasenile dementia of the Alzheimer typesevere acute respiratory syndrome coronavirus 2 global health crisissevere acute respiratory syndrome coronavirus 2 global pandemicsocial vulnerabilitysocio-economicsocio-economicallysocioeconomicallysocioeconomicsstressorvascularvascular risk factorviolentviolent behaviorworse health outcome
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Full Description

ABSTRACT
The prevention of Alzheimer’s dementia and cognitive decline in our aging population is a major public health

priority. Older Black adults are disproportionately burdened by Alzheimer’s dementia compared to other racial

and ethnic groups. Reasons for the increased burden are unknown and traditional factors, including vascular,

socioeconomic, and healthcare utilization, do not fully account for the disparity. Two important research

directions are needed to fill the current gap in knowledge regarding Alzheimer’s dementia and cognitive decline

for older Black adults, one of the most vulnerable segments of our older population. First, studies which collect

ante- and postmortem biospecimens from well-characterized older Blacks with sufficient cognitive follow-up are

needed to advance our understanding of the pathologic substrates underlying dementia. Second, the

investigation of novel factors uniquely tied to the lived experience of Blacks is essential to identify new targets

for intervention, policy, and therapeutics. The devastating effects of COVID-19 on Blacks coupled with the

increased awareness of interrelated systems of structural racism, have shone a spotlight on the importance of

race-specific stress as an understudied risk factor. It is well-documented that general stress has a negative

impact on the psychological and physical health of older Blacks, but few studies have examined the impact of

race-specific stress on brain health. The overall goal of the proposed continuation of the Minority Aging

Research Study (MARS) is to measure individual- and environmental-level race-specific stressors and identify

the biologic mechanisms linking them to late-life cognitive decline, incident AD, and other poor health

outcomes in aging. Leveraging harmonized clinical and neuropathological data from two other ongoing studies

at Rush, we will increase our sample size of Blacks to more than 1200 persons to address new Specific Aims.

We propose to continue collecting clinical and postmortem data on MARS participants, test the association of

novel race-specific stressors with cognitive decline and AD, and quantify inflammation and vascular pathology

in blood and brain, respectively, to test two potential biologic pathways linking stress to brain health in older

Blacks. Aim 1 will examine the relationship between individual and environmental race-specific stressors with

incident AD and cognitive decline. Aim 2 will leverage Medicare claims data to examine the relationship of

these stressors with other chronic vascular-related health conditions. Aim 3 will employ proteomics to measure

inflammatory proteins in plasma and examine their association with stressors and AD. Finally, Aim 4 will

examine the association of stressors with vascular neuropathologies and microglia measured in the brain, and

test whether these pathologies account for the association of race-specific stress with AD. The proposed study

provides a unique opportunity to answer critical questions about a large understudied segment of our aging

society and incorporates race-specific risk factors that have not been examined in clinical-neuropathologic

studies.

Grant Number: 5R01AG022018-16
NIH Institute/Center: NIH

Principal Investigator: Lisa Barnes

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