grant

A Comparative Analysis of Age Differences in Social Networks

Organization GEORGIA STATE UNIVERSITYLocation ATLANTA, UNITED STATESPosted 16 Sept 2025Deadline 31 May 2027
NIHUS FederalResearch GrantFY2025AgeAge associated cognitive deficitAge associated cognitive dysfunctionAge related memory declineAge related memory deficitAge related memory impairmentAge-associated cognitive declineAge-related cognitive declineAgingAwardAwarenessBarberingBenign senescent forgetfulnessBiological AgingBiological MarkersBloodBlood Reticuloendothelial SystemBrainBrain Nervous SystemBuffersCapuchin MonkeyCaringCebusCognitionCognitiveCognitive DisturbanceCognitive ImpairmentCognitive agingCognitive declineCognitive function abnormalComplexDisturbance in cognitionEmotionalEncephalonExhibitsFoodFosteringFundingFutureGroomingHealthHumanImpaired cognitionIndividualInterventionInvestigatorsK-18K-18 conjugateK18K18 combinationLeadLeftLifeLinkLonelinessMeasuresMentorsModelingModern ManMotivationNational Institutes of HealthNeocortexNerve DegenerationNeuron DegenerationNeuronal InjuryObservation researchObservation studyObservational StudyObservational researchOlder PopulationOutcomePathologicPathologyPatternPb elementPersonal SatisfactionPersonsPhysiologicPhysiologicalPlayPopulationPositionPositioning AttributePrimatesPrimates MammalsReportingResearchResearch PersonnelResearch ResourcesResearchersResource AllocationResourcesRoleSocial BehaviorSocial ChangeSocial NetworkSocial isolationSocial modificationSocial transformationTestingTimeTrainingUnited States National Institutes of Healthage associatedage associated alterationsage associated changesage associated cognitive impairmentage associated declineage associated differenceage associated effectsage associated memory declineage associated memory deficitage based differenceage correlatedage correlated alterationsage correlated changesage dependentage dependent alterationsage dependent changesage dependent declineage dependent differenceage dependent variationage differenceage effectage induced alterationsage induced changesage linkedage relatedage related alterationsage related changesage related cognitive deficitage related cognitive dysfunctionage related cognitive impairmentage related declineage related differenceage related effectsage related memory dysfunctionage related variationage specificage specific alterationsage specific changesage specific differenceage-associated memory impairmentage-induced cognitive declineage-related decline in cognitionage-related decline in cognitive functionagesaging associated alterationsaging associated changesaging biological markeraging biomarkeraging correlated alterationsaging correlated changesaging dependent alterationsaging dependent changesaging effectaging induced alterationsaging induced changesaging markeraging related alterationsaging related changesaging related cognitive declineaging specific alterationsaging specific changesalterations with agebehavior predictionbehavioral predictionbio-markersbiologic markerbiological process of agebiomarkercapuchinchanges with agecognitive abilitycognitive assessmentcognitive dysfunctioncognitive functioncognitive losscognitive testingcomparativecomputerizeddecline with agedevelop therapydiffer by agedifference across agedifference in ageexecutive controlexecutive functionexperiencehealthspanhealthy aginghealthy human aginghealthy life spanheavy metal Pbheavy metal leadhomotypical corteximpact of ageinfluence of ageinsightinterdisciplinary collaborationinterestintervention developmentisocortexlate in lifelate lifelater in lifelater lifelife historylife spanlifespanlonelymortalityneopalliumneural degenerationneurodegenerationneurodegenerativeneurological degenerationneuron injuryneuronal degenerationneuropathologicneuropathologicalneuropathologynon-human primatenonhuman primateold ageolder adultolder adulthoodolder groupsolder individualsolder personpreferencepreservationresponseskillssocialsocial cognitionsocial implicationsocial learningsocial relationshipssocial rolesociobehaviorsociobehavioralspecies differencestemtheoriestherapy developmenttooltraittransdisciplinary collaborationtreatment developmentvariation by agewell-beingwellbeing
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Full Description

PROJECT SUMMARY
Strong social relationships are essential for health and well-being, especially in later life. However, as people

age, their social networks shrink, raising concerns about social isolation and its negative effects on older adults’

health. Socioemotional selectivity theory (SST) suggests this narrowing of social networks is not necessarily

detrimental, but instead reflects a shift in older adults’ priorities. According to SST, as people get older, they

become more aware that their time left to live is limited, and this leads them to selectively focus on emotionally

meaningful relationships. SST asserts that these social changes should be unique to humans, as they exclusively

possess the ability to contemplate their mortality and future time horizons.

However, recent research challenges this human-centric view. Nonhuman primates also exhibit age-related

reductions in social networks, despite lacking the cognitive ability to reflect on mortality. Evidence of social

selectivity in nonhuman primates suggests that age-related network narrowing may be a more universal adaptive

response to cognitive decline. Prior research shows that as cognitive abilities decline with age, individuals shift

from exploration (seeking new opportunities) to exploitation strategies (making use of known resources). This

shift could explain why older individuals across species prioritize established relationships over exploring new

ones, as this is a strategy that could optimize resource efficiency in later life.

This project will examine age-related differences in the social networks of capuchin monkeys, comparing

these patterns to those observed in humans. We expect to replicate prior reports of age differences in social

network size in both species (Aim 1). Additionally, we will test whether cognitive abilities (Aim 2) or explore-

exploit tendencies (Aim 3) account for age-related differences in social behavior. Finally, the project will examine

how age differences in social behavior are linked to biomarkers sensitive to physiological aging and

neuropathology, to provide insight into the health implications of these patterns (Aim 4).

In addition to advancing our understanding of social aging, this project will equip Dr. Barber with essential

training in comparative research. Dr. Barber is an established NIH-funded investigator whose research focuses

on social and cognitive aging in humans. Her interest in this project stems from her previous research testing

tenants of SST in humans. While Dr. Barber has no prior experience working with nonhuman primates, this K18

award will provide her with the skills needed to conduct cross-species aging research and foster interdisciplinary

collaborations. Her training will be enhanced through formal coursework in primatology and directed readings in

comparative aging, overseen by her mentor, Dr. Karen Bales. Upon completing the proposed K18 activities, Dr.

Barber will be well-positioned to lead comparative aging research and to explore factors that contribute to species

differences in healthspan and lifespan.

Grant Number: 1K18AG095817-01
NIH Institute/Center: NIH

Principal Investigator: Sarah Barber

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