grant

Adult Cognitive and Neurobiological Indicators of Aging: Impact of Adversity and Social Support

Organization UNIVERSITY OF MINNESOTALocation MINNEAPOLIS, UNITED STATESPosted 15 Sept 2022Deadline 31 May 2027
NIHUS FederalResearch GrantFY202521+ years oldAddressAdultAdult HumanAdverse ExperienceAdverse eventAgeAgingAmmon HornAnimalsApproaches to preventionBehavioralBehavioral ResearchBiologicalBirthBrainBrain Nervous SystemBuffersChronicCognitionCognitiveCognitive agingCohort StudiesConcurrent StudiesCornu AmmonisDNA MethylationDataData AnalyticsDevelopmentEmotionsEncephalonEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessEventExposure toFoundationsGeneralized GrowthGeneticGrowthHippocampusHumanIndividualInterceptInterventionIntervention StrategiesInvestigationLengthLifeLife CycleLife Cycle StagesLinkLongitudinal StudiesMeasuresMethodologyMinnesotaModelingModern ManNeurobiologyNeurophysiology - biologic functionOutcomeParticipantParturitionPoliciesPrefrontal CortexPreventative strategyPreventionPrevention approachPrevention strategyPreventive strategyPublic HealthResearchRetrospective StudiesRiskRoleSamplingSensorimotor functionsSocial supportStructureTechniquesTestingTissue GrowthVariantVariationWorkaccelerated agingaccelerated biological ageaccelerated biological agingadulthoodage accelerationage associatedage associated alterationsage associated changesage associated declineage correlatedage correlated alterationsage correlated changesage dependentage dependent alterationsage dependent changesage dependent declineage induced alterationsage induced changesage linkedage relatedage related alterationsage related changesage related declineage specificage specific alterationsage specific changesagesaging associated alterationsaging associated changesaging biological markeraging biomarkeraging correlated alterationsaging correlated changesaging dependent alterationsaging dependent changesaging induced alterationsaging induced changesaging induced epigenetic changeaging markeraging processaging related alterationsaging related changesaging specific alterationsaging specific changesaging-associated epigenetic changeaging-related epigenetic changealterations with agebiobehaviorbiobehavioralbiologicbiological systemsbrain healthcare givingcaregivingchanges with agecognitive functionconnectomecostdecline with agedesigndesigningdevelopmentalearly adversityearly childhood adversityearly experienceearly life adversityepigenetic agingepigenetic biomarkerepigenetic markerepigenetic mechanisms in agingepigenetic modifications in agingepigenetic regulation of agingepigenetic variationepigeneticallyexperiencehippocampallife courselong-term studylongitudinal data setlongitudinal datasetlongitudinal outcome studiesneural functionneurobiologicalneuron toxicityneuronal toxicityneurotoxicitynovelontogenyphysical conditioningphysical healthprospectivepsychosocialpublic health relevancesocial relationshipssocial rolesocial support networktelomere
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Full Description

Project Summary/Abstract
Using a unique longitudinal data set and linear growth modeling analytic techniques, the

proposed research will examine relations between early and life course trajectories of adversity

and adult biobehavioral markers of aging. Animal and human studies suggest that early

exposure to adversity may negatively impact developing biological systems altering long term

structural and functional trajectories, and accelerating aging processes. The proposed research

will examine this neurotoxicity hypothesis in relation to brain neurobiology (structure, function,

connectivity) and related cognitive and epigenetic markers sensitive to adversity and aging. The

research will also examine the role of protective social relationships (especially positive early

caregiving) in moderating the adversity-related effects.

Based in the Minnesota Longitudinal Study of Risk and Adaptation (Sroufe et al., 2005) and

drawing on methodology from the Human Connectome Project in Aging (HCP-A; Bookheimer et

al., 2019), the study addresses significant gaps in both neurobiological and behavioral

investigations of the origins of adult aging processes and the effects of adversity on

development. Unlike concurrent and retrospective studies of risk and protective influences on

aging, the proposed study employs a prospective multilevel design with a sample of individuals

assessed from birth to middle adulthood. The proposed assessments of neurobiological and

cognitive functioning will contribute to an understanding of the impact of exposure to adversity

on adult brain health (structure, function, connectivity) and age-related cognition. Specifically,

we will examine the timing and chronicity (onset and trajectory) of adversity in relation to adult

outcomes. Genetic data will permit analyses of associations between adversity, epigenetic

variation (i.e., telomere length, DNA methylation age), and concurrent neural and cognitive

functioning. The proposed work will address critical research, policy, and practice questions

regarding the effects of adverse experience on the human brain, the cognitive and

biological correlates of neurobiological change, and the potential moderating influence of

early caregiving experience on these relations, generating testable research hypotheses

and contributing to the development of targeted prevention and intervention efforts.

Grant Number: 5R01AG070138-04
NIH Institute/Center: NIH

Principal Investigator: ELIZABETH CARLSON

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