grant

Phenotyping and Biospecimen Core

Organization BOSTON UNIVERSITY MEDICAL CAMPUSLocation BOSTON, UNITED STATESPosted 30 Sept 2021Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY2025100+ years oldA β-42A β42A-beta 42A-beta42AD dementiaAbeta-42Abeta42AffectAgeAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimer's biomarkerAlzheimer's disease biological markerAlzheimers DementiaAlzheimer’s biological markerAlzheimer’s disease biomarkerAmentiaAmyloid beta-42Amyloid beta42Amyloid β-42Amyloid β42Amyloidβ-42Amyloidβ42Anatomic SitesAnatomic structuresAnatomyAreaAssayAutopsyAβ-42Aβ42BioassayBiologicalBiological AssayBiological MarkersBlood PlasmaBlood SampleBlood specimenBody TissuesBostonBrainBrain Nervous SystemCOVID-19CV-19CentenarianClinical DataCognitiveCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalConsensusCoronavirus Infectious Disease 2019DataData CollectionDedicationsDementiaDiagnosisDisease MarkerDisturbance in cognitionEligibilityEligibility DeterminationEncephalonEnrollmentEnsureFamiliarityFastingFundingFutureGene ExpressionGene TranscriptionGeneticGenetic TranscriptionImpaired cognitionImpairmentInvestigationInvestigatorsKnowledge PortalKnowledge base PortalKnowledgebase PortalLeadLength of LifeLinkLongevityLos AngelesMarried PersonsMeasuresMissionModelingMolecularNeurocognitiveNeuropsychologic TestsNeuropsychological TestsNeuropsychologiesNeuropsychologyNew York CityNon-Polyadenylated RNAOlder PopulationOutcomeParticipantPathologicPatient RecruitmentsPb elementPhenotypePlasmaPlasma SerumPrimary Senile Degenerative DementiaProtocol ScreeningRNARNA ExpressionRNA Gene ProductsResearch PersonnelResearch ResourcesResearchersResistanceResourcesReticuloendothelial System, Serum, PlasmaRibonucleic AcidSamplingScanningSecureSpousesStatistical Data AnalysesStatistical Data AnalysisStatistical Data InterpretationSystemTissuesTranscriptionWorkagesbio-markersbiobankbiologicbiologic markerbiomarkerbiorepositorycentenarian human (100+)cognitive dysfunctioncognitive functioncognitive lossconferenceconventioncoronavirus disease 2019coronavirus disease-19coronavirus infectious disease-19cytokinedata de-identificationdata deidentificationdata managementdata sharingde-identified datadeidentified dataenrollexomeexperiencefastedfastsheavy metal Pbheavy metal leadinnovateinnovationinnovativenecropsyneural imagingneuro-imagingneuroimagingneurological imagingneuropathologicneuropathologicalneuropathologyneuropsychologicoffspringolder groupsolder individualsolder personparticipant enrollmentparticipant recruitmentpatient enrollmentphenotypic datapostmortemprimary degenerative dementiaprotective factorsrecruitresilienceresilientresistantsenile dementia of the Alzheimer typestatistical analysissuccesssummitsuper agersymposiasymposiumtooltranscriptomicstranslational opportunitiestranslational potentialvirtual
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Full Description

The Phenotyping and Biospecimen (P&B) Core's primary mission is to leverage two NIA-funded centenarian
studies by sifting through their study participants in identifying centenarian cognitive superagers, offspring and

offspring spouses for enrollment in the RADCO study, extending their phenotyping with annual uniform

neuropsychological testing, plasma biomarkers of Alzheimer's disease (AD), and facilitating and facilitating

neuroimaging and post-mortem neuropathological studies among willing participants. The P&B Core's

successful conduct of its six aims is critical to RADCO's investigation of centenarians and their offspring as

models of cognitive resilience and resistance to cognitive impairment and AD. Those 6 Specific Aims are:

Specific Aim 1. Establish a cognitive superagers (n=496, ages 100-110 years), offspring (n=600), and offspring

spouses (n=120) sample with baseline neuropsychological assessments, other phenotypic data, blood samples,

and genetic and biomarker data provided by 2 ongoing NIA-funded centenarian studies. Specific Aim 2. Perform

annual Covid-19-safe virtual neurocognitive assessments and other phenotypic data collection that are uniform

with the ILO study and LCCP measures. Also, to enhance accuracy of the neurocognitive assessments by

performing interdisciplinary expert diagnoses consensus conferences. Specific Aim 3. Employing REDCap,

manage and perform QC, and make easily but securely available all of the data collected and generated by the

RADCO Cores and Projects, including the neuropsychological, neuroimaging, neuropathologic phenotype and

biomarker and transcriptomic data. Specific Aim 4. To receive from the ILO+LCCP studies and then

longitudinally collect blood samples (centenarians annually, offspring and offspring spouses every other year)

from RADCO participants for use by the two projects. To maintain samples in a biorepository as a sharable

resource. Specific Aim 5. Support the RADCO Neuroimaging Core's aims by recruiting RADCO participants for

local neuroimaging and linking scan data to clinical data. Specific Aim 6. Recruit RADCO participants for future

brain donation, ensure that autopsies proceed smoothly, and link clinical data to anatomic, pathologic and

molecular data generated by the P&B neuropathology efforts. These data will inform the resilient and resistant

phenotypes delineated in Project 1. Brain area-specific tissues will be provided for RNA expression studies in

Project 2.

Grant Number: 5U19AG073172-05
NIH Institute/Center: NIH

Principal Investigator: Stacy Andersen

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