grant

Visceral neural circuits linking childhood threat and deprivation with stress physiology and affective symptoms in a transdiagnostic sample using high-field personalized brain mapping

Organization UNIVERSITY OF PITTSBURGH AT PITTSBURGHLocation PITTSBURGH, UNITED STATESPosted 19 Jul 2019Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY2023Aeroseb-HCAffectiveAffective DisordersAffective SymptomsAgeAmmon HornAmygdalaAmygdaloid BodyAmygdaloid NucleusAmygdaloid structureAnteriorAnxietyBed Nucleus of Stria TerminalisBrainBrain MappingBrain Nervous SystemBrain StemBrain regionBrainstemCatecholaminesCell Communication and SignalingCell NucleusCell SignalingCetacortChild AbuseChildhoodChildhood AbuseChronic stressClinicalCommunitiesCornu AmmonisCort-DomeCortefCortenemaCortisolCortisprayCortrilDataDermacortDiagnosticDiseaseDisorderDistalDropoutEldecortEmotionalEmotionsEncephalonFaceFearFore-BrainForebrainFrightGlucocorticoidsHairHippocampusHydrocortisoneHydrocortoneHypothalamic structureHypothalamusHytoneIndividualIndividual DifferencesInterventionIntervention StrategiesIntracellular Communication and SignalingLinkLiteratureMR ImagingMR TomographyMRIMRIsMagnetic Resonance ImagingMapsMeasuresMediatingMedical Imaging, Magnetic Resonance / Nuclear Magnetic ResonanceMental HealthMental HygieneMental disordersMental health disordersMethodologyModelingMood DisordersMoodsNIMHNMR ImagingNMR TomographyNational Institute of Mental HealthNeighborhoodsNoiseNuclear Magnetic Resonance ImagingNucleusNucleus Tractus SolitariiNucleus solitariusNutracortOutcomeParaventricular Hypothalamic NucleusPathway interactionsPhasePhysiologicPhysiologicalPhysiologyPre-Clinical ModelPreclinical ModelsProctocortProsencephalonPsyche structurePsychiatric DiseasePsychiatric DisorderPsychiatryPsychological HealthPsychopathologyPublic HealthRDoCResearchResearch Domain CriteriaResolutionRestRisk FactorsSalivarySamplingSeveritiesSexual abuseSignal TransductionSignal Transduction SystemsSignalingSocio-economic statusSocioeconomic StatusSolitary NucleusStimulusStressStria Terminalis NucleusStructureStructure of terminal stria nuclei of preoptic regionSympathinsThinkingTranslatingTraumaVisceralVisualizationZeugmatographyabnormal psychologyadult youthagesamygdaloid nuclear complexbiological adaptation to stressbiological signal transductionchildhood adversitycingulate cortexconnectomedeprivationenvironmental stressesenvironmental stressorexcitotoxicexcitotoxicityexperiencefacesfacialhippocampalhypothalamicimprovedinterestinterventional strategylow SESlow socio-economic positionlow socio-economic statuslow socioeconomic positionlow socioeconomic statusmentalmental illnessmulti-modal neuro-imagingmulti-modal neuroimagingmultimodal neuro-imagingmultimodal neuroimagingneuralneural circuitneural circuitryneurocircuitrynovelparaventricular nucleuspathwaypediatricpediatric adversityphysical abusephysical conditioningphysical healthphysical maltreatmentpsychiatric illnesspsychological disorderreaction; crisisrecruitresolutionsresponsesex abusesexually abusedsocio-economic positionsocioeconomic positionsolitary tract nucleusstress reactivitystress responsestress; reactionsubstantia albasuper high resolutionsuperresolutionsynaptic circuitsynaptic circuitrythoughtstraumatic eventultra high resolutionurinarywhite matteryoung adultyoung adulthood
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Project Summary/Abstract
Childhood adversity was recently posited to be psychiatry's greatest public health challenge, as it is a major

predictor of mood, anxiety and trauma-related (i.e., affective) disorders. Childhood adversity is also associated

with dysregulated physiological stress reactivity, which individuals with affective disorders also display. While

stress is thought to be a mechanism by which childhood adversity influences physical and mental health, few

studies have considered stress-related brain regions beyond corticoamygdalar and hippocampal structures

and little is known regarding how childhood adversity impacts specific, proximally stress-responsive neural

circuits. Central visceral circuits (CVCs) are implicated in affective psychopathology and are critical in the

control of stress responses. CVCs comprise visceromotor and viscerosensory pathways that reciprocally

connect hypothalamic and limbic forebrain regions to brainstem nuclei. Preliminary data show significant links

between: 1) childhood adversity and CVCs and 2) CVCs and affective symptoms. These results also suggest

opposing influences of childhood “threat” vs. “deprivation” on CVCs. “Threat” experiences include abuse and

other traumatic events, while “deprivation” comprises diminished environmental stimuli, such as low childhood

socioeconomic status or neighborhood deprivation. Interestingly, evidence suggests that threat blunts, while

deprivation heightens physiological stress reactivity (e.g., cortisol reactivity). Thus, we propose that threat and

deprivation may have different effects on the CVCs most proximal to the control of stress responses, including

understudied regions such as the brainstem nucleus of the solitary tract (NST), paraventricular nucleus of the

hypothalamus (PVN) and bed nucleus of the stria terminalis (BST). In the proposed, limitations of lower field

strength MRI are overcome with the improved signal-to-noise and unprecedented resolution of high-field MRI

at 7 Tesla. Multimodal neuroimaging will acquire specialized structurals, and resting-state, mental stress and

emotion-evoked, and white matter connectivity. Stress physiology measures will also be collected. Consistent

with the RDoC initiative, we will recruit a continuous and transdiagnostic community sample of 220 young

adults (ages 18-35) with a full range of childhood threat, deprivation and affective symptoms to examine: 1) the

effects of childhood threat and deprivation on CVC connectivity, 2) the effects of childhood threat and

deprivation on stress physiology and affective symptoms, and 3) the extent to which CVC connectivity

mediates the relationship between threat and deprivation, and physiological and affective outcomes.

Significance. Our proposal is congruent with NIMH Strategy 1.3, Map the connectomes for mental illnesses,

focusing on CVCs as the “connectome” of interest. Elucidating how CVCs may link childhood threat and

deprivation to stress physiology and affective symptoms using high-field personalized brain mapping may

enhance our ability to translate findings from preclinical models and may guide clinical thinking by providing

novel proximally stress-responsive targets and/or novel or integrative approaches for intervention.

Grant Number: 5R01MH120065-05
NIH Institute/Center: NIH

Principal Investigator: Layla Banihashemi

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