Aging Research Characterizing Health Equity via Social determinants (ARCHES)
Project Number5R01AG074302-04
Contact PI/Project LeaderBABULAL, GANESH M Other PIs
Awardee OrganizationWASHINGTON UNIVERSITY
Description
Abstract Text
PROJECT SUMMARY/ABSTRACT
Our long-term goal is to employ innovative community based participatory research to establish a
community advisory board, to collaborate with our community partners to recruit, enroll, and retain a cohort of
Black participants and, then, to examine causal mechanisms that increase the risk of Alzheimer disease (AD)
within the community cohort. The long preclinical stage of AD, as reflected in biomarkers among adults, is a
key risk factor of symptomatic AD. However, despite Blacks having a higher risk of developing AD, recent
studies suggest that they have less abnormal levels of biomarkers than Whites in cognitively normal samples.
This study aims to examine other risk factors of cognitive decline and AD such as depression, stress, and
social determinants of health (SDOH) in a representative sample of Black participants.
This research is significant because there are nearly 46 million Black Americans, comprising 13% of the
population in the United States. The Black older adult population is expected to increase, from 4.4 million older
adults in 2016 to 12.1 million by 2060. Despite these demographic projections, Blacks are significantly
underrepresented in AD research. An almost exclusive focus on Whites has created a knowledge gap in
understanding how SDOH mechanisms affect diverse populations. Closing this knowledge gap soon is critical
since epidemiological studies suggest that Blacks are at twice the risk of AD compared to Whites.
Our Specific Aims will (1) Establish a cohort of middle-to-older age Black adults (N=300) using community-
based participatory research to understand the unique social, environmental, and economic barriers related to
AD risk, (2) Determine the impact of depression, stress, and a novel, theory-based SDOH composite index (CI)
on cognitive functioning in participants who are cognitively normal with and without preclinical AD, and (3) Test
the association between white matter hyperintensities (WMH) and hippocampal volume (HV) with the SDOH-CI
in a subset of participants (N=150) with magnetic resonance imaging (MRI) data.
To test our Aims, we have assembled a multidisciplinary team with expertise in AD, SDOH, community-
based participatory research and system dynamics, community mobilization, stress and depression, plasma
biomarkers, genetics, neuroimaging, neuropsychology, and biostatistical methods. Participants will undergo a
one-time blood draw for AD biomarker profiling, cognitive assessment using a neuropsychological battery, and
participate in one MRI scan session. Participants will also participate in workshops, complete a comprehensive
battery of SDOH measures mapped onto the National Institute of Aging’s Health Research Disparities
Framework, and clinical, neurological, and neuropsychological tests annually for up to five years.
Once obtained, this knowledge of how within-group heterogeneity in cognitive functioning and AD risk is
impacted by SDOH may better support effective AD intervention and treatment for Black Americans.
Public Health Relevance Statement
PROJECT NARRATIVE
Our long-term goal is to employ innovative community based participatory research principles to establish a
community advisory board, to collaborate with our community partners to recruit, enroll, and retain a cohort of
Black participants and, then, to examine causal mechanisms that increase the risk of preclinical and
symptomatic Alzheimer disease (AD) within our cohort. Despite the growing older adult population and
epidemiological studies suggesting that Blacks are at twice the risk of developing AD compared to Whites, and
Blacks are severely underrepresented in AD research. This study aims to create a representative sample of
Black participants and examine how risk factors of AD such as depression, stress, and social determinants of
health impact cognitive functioning and preclinical AD.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AdultAffectAgingAlzheimer disease preventionAlzheimer's DiseaseAlzheimer's disease pathologyAlzheimer's disease riskAlzheimer’s disease biomarkerAmyloid ProteinsAwarenessBehavioralBiologicalBiological MarkersBiological ModelsBiostatistical MethodsBlack AmericanBlack PopulationsBlack raceBloodCerebrospinal FluidChronic stressClinicalCognitionCognitiveCollaborationsCommunitiesComplexCoping BehaviorDataDementiaDetectionDevelopmentDiagnosisDiscriminationEconomicsEducationEducational workshopEmploymentEnrollmentEnvironmental Risk FactorExposure toGeneticGenomicsGoalsHealthHealth Disparities ResearchHeterogeneityHippocampusImageImpaired cognitionInflammationInflammatoryInterventionKnowledgeLife Cycle StagesLife StyleLinkMRI ScansMagnetic Resonance ImagingMapsMeasuresMediatorMental DepressionMethodsModelingMolecularNational Institute on AgingNeighborhoodsNerve DegenerationNeurologicNeuropsychological TestsNeuropsychologyParticipantPlasmaPopulationPopulation HeterogeneityPopulation StudyPrevalenceRecording of previous eventsResearchResearch MethodologyResourcesRiskRisk FactorsSample SizeSamplingSocioeconomic StatusStressSymptomsTestingUnited StatesValidationVascular DiseasesWhite Matter HyperintensityWorkbrain healthcognitive functioncognitive testingcohortcommunity advisory boardcommunity based participatory researchcommunity partnersdementia riskdepressive symptomsdynamic systemepidemiology studyfollow-uphealth care availabilityhealth care service utilizationhealth equityhealthy aginghigh riskhuman old age (65+)indexinginflammatory markerinnovationlongitudinal, prospective studymultidisciplinaryneuroimagingnovelolder adultparticipant retentionpre-clinicalpsychosocialrecruitscreeningsocialsocial culturesocial determinantssocial factorssocial health determinantssocioeconomicssuburbtau Proteinstheoriestrustworthiness
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Publications
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