grant

VULNERABILITY AND RESILIENCY IN THE AGING ADULT BRAIN CONNECTOME (AABC)

Organization WASHINGTON UNIVERSITYLocation SAINT LOUIS, UNITED STATESPosted 30 Sept 2021Deadline 31 Mar 2027
NIHUS FederalResearch GrantFY2025100+ years old21+ years oldAD dementiaAD related dementiaADRDActive Follow-upAdultAdult HumanAffectAgingAlzheimer Type DementiaAlzheimer beta-ProteinAlzheimer disease dementiaAlzheimer risk factorAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's Amyloid beta-ProteinAlzheimer's DiseaseAlzheimer's amyloidAlzheimer's and related dementiasAlzheimer's biomarkerAlzheimer's dementia and related dementiaAlzheimer's dementia or related dementiaAlzheimer's disease and related dementiaAlzheimer's disease and related disordersAlzheimer's disease biological markerAlzheimer's disease or a related dementiaAlzheimer's disease or a related disorderAlzheimer's disease or related dementiaAlzheimer's disease related dementiaAlzheimer's disease riskAlzheimers DementiaAlzheimer’s biological markerAlzheimer’s disease biomarkerAmentiaAmyloid Alzheimer's Dementia Amyloid ProteinAmyloid Beta-PeptideAmyloid Protein A4Amyloid beta-ProteinAmyloid βAmyloid β-PeptideAmyloid β-ProteinBehaviorBiologicalBiological MarkersBloodBlood PlasmaBlood PressureBlood Reticuloendothelial SystemBrainBrain Nervous SystemCentenarianClinicalCognitionCognitiveCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalCommunitiesConceptionsDataData AnalysesData AnalysisData BasesDatabasesDementiaDevelopmentDietDimensionsDiseaseDisorderDisturbance in cognitionEarly identificationEncephalonEnrollmentEnsureFoundationsFundingGeneral PopulationGeneral PublicGeneticGoalsHealthHumanHuman ResourcesImageImage AnalysesImage AnalysisImpaired cognitionImpairmentIndividualInflammationInformaticsInfrastructureInvestigatorsLeadershipLifeLife StyleLifestyleLightMR ImagingMR SpectroscopyMR TomographyMRIMRIsMagnetic Resonance ImagingMagnetic Resonance SpectroscopyManpowerMapsMedical Imaging, Magnetic Resonance / Nuclear Magnetic ResonanceMenopauseMissionModern ManMultimodal ImagingMultiomic DataNIH RFANMR ImagingNMR TomographyNational Institutes of HealthNeurocognitiveNuclear Magnetic Resonance ImagingParticipantPathologyPatternPerimenopausalPerimenopausePhase TransitionPhenotypePhotoradiationPhysical activityPhysiologicPhysiologicalPlasmaPlasma SerumPopulationPost-MenopausePost-menopausal PeriodPostmenopausal PeriodPostmenopausePrimary Senile Degenerative DementiaProbabilistic ModelsProbability ModelsProtocolProtocols documentationQuality ControlRaceRacesRequest for ApplicationsResearch PersonnelResearch ResourcesResearch SpecimenResearchersResistanceResolutionResourcesReticuloendothelial System, Serum, PlasmaRiskRisk FactorsRunningSamplingSiteSpecimenStandardizationStatistical ModelsStressStructureSymptomsTimeUnderrepresented GroupsUnderrepresented PopulationsUnited States National Institutes of HealthWomanZeugmatographya beta peptideabetaactive followupadulthoodafter menopauseagedallostatic loadalzheimer riskamyloid betaamyloid-b proteinbeta amyloid fibrilbio-markersbiologicbiologic markerbiomarkercentenarian human (100+)cognitive assessmentcognitive changecognitive dysfunctioncognitive losscognitive testingcohortconnectomedata acquisitiondata acquisitionsdata basedata integrationdata interpretationdata sharingdata sharing networksdata sharing resourcedevelopmentaldietsenrollfollow upfollow-upfollowed upfollowing menopausefollowupgenetic informationimage evaluationimage interpretationimaginglack of physical activitylate in lifelate lifelife spanlifespanmenopause transitionmulti-modal imagingmulti-modality imagingmultimodality imagingmultiomicsmultiple omic datamultiple omicsneuralneural imagingneural inflammationneuro-imagingneurochemicalneurochemistryneurofilamentneuroimagingneuroinflammationneuroinflammatoryneurological imagingnovelp-taup-τpanomicspast menopauseperi-menopausalperi-menopausepersonnelphenotypic dataphospho-tauphospho-τphosphorylated tauphysical inactivitypost-menopausalpost-translational modification of taupostmenopausalpostmenopausal statusposttranslational modification of taupre-clinicalpreclinicalpreservationprimary degenerative dementiapsychologicpsychologicalquality of sleepracialracial backgroundracial originrecruitresilienceresilience factorresiliency factorresilientresistantresolutionsresponsesenile dementia of the Alzheimer typesexsleep qualitysocialsoluble amyloid precursor proteinstatistical analysis corestatistical corestatistical linear mixed modelsstatistical linear modelsstatistics corestatistics research coretau phosphorylationtau posttranslational modificationtau-1transition to menopausetransitional menopauseunder representation of groupsunder represented groupsunder represented peopleunder represented populationsunderrepresentation of groupsunderrepresented peoplevasomotor symptomsτ phosphorylation
Sign up free to applyApply link · pipeline · email alerts
— or —

Get email alerts for similar roles

Weekly digest · no password needed · unsubscribe any time

Full Description

ABSTRACT FOR OVERVIEW
The Aging Adult Brain Connectome (AABC) leverages the existing infrastructure developed by the Human

Connectome Project for Aging (HCP-A) by obtaining longitudinal follow-up data (neuroimaging, cognitive testing,

and blood) using a standardized protocol from a well characterized cohort of over 1,000 healthy individuals to

generate within-participant brain trajectories for up to 10 years. At initial recruitment, individuals enrolled in the

HCP-A were generally physically and cognitively healthy but over time some will develop preclinical AD or early

cognitive changes due to AD or ADRD. The AABC is comprised of four Projects: Project 1 examine the effects

of stress and allostatic load, including inflammation, during the early adult period. Project 2 examines the effects

of lifestyle behaviors on the trajectory of cognitive and brain changes during the mid adult period. Project 3

examine the effects of menopause transition/vasomotor symptoms during the mid adult period. Project 4 exam-

ine the clinical and neural indicators of resiliency and resistance to AD and ADRD in the later decades of adult-

hood. The AABC also consists of 4 Cores: The Administration Core (AC) will provide essential core and site

leadership to carry out the scientific mission of the AABC. The diversity recruitment and retention unit (DRRU)

will be located within this core and will ensure that the AABC continues to recruit and retain an adequate distri-

bution of races that is currently seen in the US. The Integrated Data Acquisition Core (IDAC) provides expertise

and personnel from each site to acquire high quality neuroimaging, deep phenotyping of non-imaging data, and

biosamples from each site.The Informatics, Data Analysis, and Statistics Core (IDASC) will house project imag-

ing data using the IntraDB database, will perform quality control of raw and analyzed data, will develop and run

cross-sectional and longitudinal pipelines to produce multi-modal imaging data phenotypes for each project, will

provide dimension-reduced summaries, will impute missing data; and will develop and run statistical models for

each project. The IDASC will also be responsible for data sharing with the general public. The Genetics and

Multi-omics Specimens Core (GMSC) will provide genetic information on participants evaluated through the

AABC who have been characterized using a uniform protocol. Multi-omic data and AD biomarker data will be

generated by the GMSC.

Grant Number: 5U19AG073585-04
NIH Institute/Center: NIH

Principal Investigator: Beau Ances

Sign up free to get the apply link, save to pipeline, and set email alerts.

Sign up free →

Agency Plan

7-day free trial

Unlock procurement & grants

Upgrade to access active tenders from World Bank, UNDP, ADB and more — with email alerts and pipeline tracking.

$29.99 / month

  • 🔔Email alerts for new matching tenders
  • 🗂️Track tenders in your pipeline
  • 💰Filter by contract value
  • 📥Export results to CSV
  • 📌Save searches with one click
Start 7-day free trial →