Cycles of Social Contingency in Autism: Pivotal Transitions that Shape Infant Brain-Behavior Development in Human & Model Systems
Project Number2P50MH100029-06
Former Number9P50HD093082-06
Contact PI/Project LeaderKLIN, AMI
Awardee OrganizationEMORY UNIVERSITY
Description
Abstract Text
PROJECT SUMMARY
The Emory ACE joins 12 laboratories in 6 institutions under the auspices of Emory University, creating a center
for clinical and translational science built – from its outset – on the expectation of transformative impact on the
community. These laboratories combine methodological and conceptual expertise in child development, speech
science, behavioral neuroscience, and treatment research. The thematic mission of the Emory ACE guides each
of its 5 projects and 4 cores: to execute science that leads directly to a future of optimized outcomes for the next
generations of children with autism spectrum disorder (ASD). Projects I-III study reciprocal behavior, in the visual
and vocal, brain and behavior domains, within the first six months of life, and in subsequent brain-behavior
transitions until 30 months of age, in infants and toddlers at low and high risk for ASD. Project IV advances
rigorous, randomized-controlled trials for treatment of ASD into infancy and toddlerhood, testing infant and infant-
caregiver characteristics that predict treatment response and outcome; its goal is to optimize treatment effects,
personalized to the developmental stage of the child, and within the structure of the child-caregiver dyad. Project
V advances a nonhuman primate model of social development, interrogating the underpinnings of social disability
in brain and behavior studies. Together, these Projects advance our understanding of the developmental
unfolding of ASD, and sets the stage for changing its course prior to the point when disability is even fully manifest.
Four Cores provide the resources to support these goals, spanning Clinical Assessment and Care, Informatics,
Administration and Dissemination & Outreach. In its efforts to meet and exceed the aspirational goals for autism
set forth by the US DHSS Interagency Autism Coordinating Committee and by NIMH Research Priorities, the
Emory ACE expands a new scientific community, focused on the translational social neuroscience of ASD, in
service of children and families. Its ultimate goal is to change the narrative of ASD from one of potentially
devastating disability to one of positive diversity, in which individuals with autism are able to succeed despite
their learning differences and because of their unique assets, unencumbered by the burdens of language,
intellectual disabilities, and severe behavior challenges.
Public Health Relevance Statement
PROJECT NARRATIVE
The Emory ACE will identify and refine quantitative measures of social brain and behavior that underlie social
and communication development, in infants at low and high risk for autism spectrum disorder, from birth through
30-33 months of age, with the goal of optimizing response to early treatment, which begins at 6-12 months
(Projects I-IV). These same constructs and measures are then shared with Project V to interrogate the
neurobiological underpinnings of species-typical social development.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AccountingAchievementAddressAffectAgeAge-MonthsAttenuatedAutistic DisorderBehaviorBehavioralBiologicalBiological ModelsBirthBrainCaregiversCharacteristicsChildChild DevelopmentClinical SciencesClinical TreatmentClinical assessmentsCommunicationCommunitiesCommunity OutreachDataDevelopmentEarly InterventionEarly treatmentEnvironmentEtiologyFamilyFutureGenesGenetic Predisposition to DiseaseGenetic RiskGoalsGrowthHealthcare SystemsHumanIndividualIndividual DifferencesInfantInformaticsInstitutionIntellectual functioning disabilityInterventionLaboratoriesLanguageLearningLettersLifeMacaca mulattaMainstreamingMeasuresMediator of activation proteinMethodologyMethodsMissionModalityModelingMonkeysNational Institute of Mental HealthNeurobiologyNeurosciencesOutcomePostdoctoral FellowRandomized Controlled TrialsResearchResearch PriorityResourcesSamplingScienceScientistSeriesServicesShapesSignal Detection AnalysisSocial DevelopmentSocial InteractionSpeechStructureSumSymptomsSystemTechniquesTechnologyTestingToddlerTranslational ResearchTreatment outcomeUniversitiesVisualWorkautism spectrum disorderbasebehavioral studybrain behaviorclinical carecohortdisabilityevidence baseexpectationfunctional outcomeshealth care deliveryhigh riskimplementation scienceinfancyinnovationnext generationnonhuman primateoutreachpredictive of treatment responseprogramsprospectiveresponsesocialsocial communicationsocial engagementsocial neurosciencesymptomatologytooltreatment effecttreatment strategy
No Sub Projects information available for 2P50MH100029-06
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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