grant

Clinical and biologic health trajectories after early life adversity

Organization CHILDREN'S HOSP OF PHILADELPHIALocation PHILADELPHIA, UNITED STATESPosted 1 Jul 2022Deadline 30 Jun 2027
NIHUS FederalResearch GrantFY20250-11 years old12-20 years old21+ years oldAbateAccountingAddressAdolescenceAdultAdult HumanAgeAttentionAwardB-Cell Differentiation Factor GeneB-Cell Stimulatory Factor 2 GeneBSF-2 GeneBSF2 GeneBehavioralBeta-2 Gene InterferonBiologicalCareer Development AwardsCareer Development Awards and ProgramsCareer Development Programs K-SeriesChildChild AbuseChild Abuse and NeglectChild HealthChild WelfareChild YouthChildhoodChildhood AbuseChildhood maltreatmentChildren (0-21)Children's HospitalClinicalClinical ImmunologyComplexDNA MethylationDataDevelopmentDiagnosisDiagnosticDifferences between sexesDiffers between sexesDimensionsDoseEmotionalEnvironmentEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessEpigenetic ageFundingFutureGene x Environment InteractionGeneral RadiologyGenesGeneticGenetic PredispositionGenetic Predisposition to DiseaseGenetic RiskGenetic SusceptibilityGenetic propensityGenomic approachGenomicsGoalsGrantGrimAge clockGurGxE interactionHSF GeneHannum clockHealthHepatocyte Stimulatory Factor GeneHorvath clockHybridoma Growth Factor GeneIFNB2 GeneIL-6 GeneIL6IL6 geneImmunologyInflammationInflammatoryInherited PredispositionInherited SusceptibilityInterleukin 6 (Interferon, Beta 2) GeneInterleukin-6 GeneInterventionInvestigatorsK-AwardsK-Series Research Career ProgramsLeadershipLong-term prospective studiesMeasurableMeasuresMedicalMental HealthMental HygieneMentorshipMethylationModernizationMorbidityMorbidity - disease rateNeurologyOutcomePTSDPaperPediatric HospitalsPediatric ResearchPediatricsPennsylvaniaPhenoAge clocksPhenotypePhiladelphiaPhysiciansPoliciesPopulation HeterogeneityPositionPositioning AttributePost-Traumatic NeurosesPost-Traumatic Stress DisordersPosttraumatic NeurosesPredispositionPsyche structurePsychiatryPsychological HealthPsychopathologyRadiologyRadiology SpecialtyReportingResearchResearch Career ProgramResearch PersonnelResearchersRiskRoleSamplingScientistSex DifferencesSexual abuseSexual differencesStressStressful EventSupervisionSusceptibilityTestingTrainingTranslational ResearchTranslational ScienceTraumaUniversitiesWorkWritingabnormal psychologyaccelerated epigenetic ageaccelerated epigenetic agingaccelerated pace of epigenetic agingacceleration in epigenetic ageadolescence (12-20)adolescent traumaadolescent welfareadulthoodagesaging induced epigenetic changeaging-associated epigenetic changeaging-related epigenetic changebiobankbiologicbiorepositorycareerchild maltreatmentchild well beingchild wellbeingchildhood adversitychildhood traumaclinical careco-morbidco-morbiditycohortcomorbiditycytokinedevelopmentaldevelopmental psychologydiverse populationsearly adversityearly childhood adversityearly life adversityentire genomeenvironment effect on geneepigenetic age clocksepigenetic agingepigenetic clockepigenetic mechanisms in agingepigenetic modifications in agingepigenetic molecular clocksepigenetic regulation of agingepigeneticallyepigenomicsexperienceexposure to traumafaster epigenetic agingfaster rates of epigenetic agingfull genomegene environment interactiongenetic etiologygenetic mechanism of diseasegenetic vulnerabilitygenetically predisposedgenomic datagenomic datasetgenomic effortgenomic strategyheterogeneous populationimprovedincreased epigenetic ageincreased epigenetic agingincreased rates of epigenetic aginginnovateinnovationinnovativeinsightkidslongitudinal, prospective studymaltreatmentmentalmethylation clockmethylomemistreatmentmortalitymulti-modalitymultimodalityneuropsychiatricneuropsychiatrypediatricpediatric adversitypediatric traumaphenomicsphysical abusephysical conditioningphysical healthphysical maltreatmentpleiotropic effectpleiotropismpleiotropypolygenetic risk scorespolygenic risk scorepopulation diversitypost-trauma stress disorderposttrauma stress disorderprofessorpsychiatric geneticspsychogeneticsrapid epigenetic agingsexsex abusesex based differencessex-dependent differencessex-related differencessex-specific differencessexually abusedskillssocial rolestressful experiencestressful life eventstressful life experiencesystemic inflammationsystemic inflammatory responsetraining opportunitytranslation researchtranslational genomicstranslational investigationtrauma exposuretrauma in childrentraumatic neurosiswhole genomeyoungster
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Full Description

Project Summary/Abstract
This career development award details a 5-year training plan to facilitate the transition of Dr. Barbara H.

Chaiyachati to an independent career as a physician-scientist studying predictors of mental and physical health

of children after trauma with an objective to identify actionable targets of intervention. Experiences of child

abuse and neglect place hundreds of thousands of children at risk for negative health outcomes every year in

the U.S. Better understanding of proximate mental and physical health predictors after childhood traumatic

stressful events (TSE), including predictive role of genetic susceptibility integrated with early biologic

embedding by epigenetic age acceleration (EAA) and increased inflammation, may facilitate targeted

interventions to ameliorate the spectrum of long-term health burdens. Thus, multimodal phenomic and genomic

approaches are needed to elucidate the complex connections between maltreatment and health. The proposed

project builds on the diverse clinical and research experiences of the candidate, with mentorship led by Dr.

Raquel Gur, the Karl and Linda Rickels Professor of Psychiatry, Neurology and Radiology at the University of

Pennsylvania and an expert in neurodevelopmental trajectories, and Dr. Hakon Hakonarson, Professor of

Pediatrics at the Children’s Hospital of Philadelphia and an expert in translational genomics. A team of

collaborators adds expertise in developmental psychology, basic and clinical immunology, psychiatric genetics,

and behavioral epigenomics, with grounding in child abuse clinical care. The research leverages large,

ancestry-diverse, adversity-exposed cohorts within established biorepositories to identify measurable,

biologically-relevant health predictors after adversity in childhood. Dr. Chaiyachati will conduct phenomic

(physical, mental health, systemic inflammation by cytokines) and genomic (whole genome and methylome)

assessments. Specifically, Aim 1 is to determine the impact of TSEs and genetic stress sensitivity, as marked

by genetic risk for PTSD, on mental and physical health in adolescence; Aim 2 will assess the impact of TSE

on epigenetic aging per DNA methylation clocks; and Aim 3 will test for increased inflammation after

experiences of maltreatment. Completion of the proposed studies will improve our understanding of mental and

physical health trajectories after experiences of trauma. This proposal will also provide the candidate with

experience studying phenomic and genomic data, writing grants and scientific papers, and allow her to gain

skills requisite for supervision and leadership. Furthermore, this proposal will establish Dr. Chaiyachati’s

intersectional research agenda and position her for independence as a physician-scientist.

Grant Number: 5K08MH129657-04
NIH Institute/Center: NIH

Principal Investigator: Barbara Chaiyachati

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