Maternal adverse childhood experiences and infant visual-limbic white matter development.

DoHAD Fractional anisotropy Intergenerational transmission Maternal adverse childhood experiences White matter microstructure

Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
25 Aug 2024
Historique:
received: 02 05 2024
revised: 06 08 2024
accepted: 23 08 2024
medline: 28 8 2024
pubmed: 28 8 2024
entrez: 27 8 2024
Statut: aheadofprint

Résumé

Maternal adverse childhood experiences (ACEs) are robust predictors of mental health for both the exposed individual and the next generation; however, the pathway through which such intergenerational risk is conferred remains unknown. The current study evaluated the association between maternal ACEs and infant brain development, including an a priori focus on circuits implicated in emotional and sensory processing. The sample included 101 mother-infant dyads from a longitudinal study. Maternal ACEs were assessed with the Adverse Childhood Questionnaire dichotomized into low (0 or 1) and high (≥2) groups. White matter microstructure, as indexed by fractional anisotropy (FA), was assessed using structural magnetic resonance imaging in infants (41.6-46.0 weeks' postconceptional age) within a priori tracts (the cingulum, fornix, uncinate, inferior frontal occipital fasciculus, and inferior longitudinal fasciculus). Exploratory analyses were also conducted across the whole brain. High maternal ACEs (≥2) were associated with decreased infant left inferior longitudinal fasciculus (ILF) FA (F(1,94) = 7.78, p < .006) relative to infants of low ACE mothers. No group difference was observed within the right ILF following correction for multiple comparisons (F(1,95) = 4.29, p < .041). Follow-up analyses within the left ILF demonstrated associations between high maternal ACEs and increased left radial diffusivity (F(1,95) = 5.10, p < .006). Exploratory analyses demonstrated preliminary support for differences in visual processing networks (e.g. optic tract) as well as additional circuits less frequently examined in the context of early life adversity exposure, (e.g. corticothalamic tract). Maternal ACEs predict neural circuit development of the inferior longitudinal fasciculus. Findings suggest that early developing sensory circuits within the infant brain are susceptible to maternal adverse childhood experiences and may have implications for the maturation of higher order emotional and cognitive circuits.

Sections du résumé

BACKGROUND BACKGROUND
Maternal adverse childhood experiences (ACEs) are robust predictors of mental health for both the exposed individual and the next generation; however, the pathway through which such intergenerational risk is conferred remains unknown. The current study evaluated the association between maternal ACEs and infant brain development, including an a priori focus on circuits implicated in emotional and sensory processing.
METHODS METHODS
The sample included 101 mother-infant dyads from a longitudinal study. Maternal ACEs were assessed with the Adverse Childhood Questionnaire dichotomized into low (0 or 1) and high (≥2) groups. White matter microstructure, as indexed by fractional anisotropy (FA), was assessed using structural magnetic resonance imaging in infants (41.6-46.0 weeks' postconceptional age) within a priori tracts (the cingulum, fornix, uncinate, inferior frontal occipital fasciculus, and inferior longitudinal fasciculus). Exploratory analyses were also conducted across the whole brain.
RESULTS RESULTS
High maternal ACEs (≥2) were associated with decreased infant left inferior longitudinal fasciculus (ILF) FA (F(1,94) = 7.78, p < .006) relative to infants of low ACE mothers. No group difference was observed within the right ILF following correction for multiple comparisons (F(1,95) = 4.29, p < .041). Follow-up analyses within the left ILF demonstrated associations between high maternal ACEs and increased left radial diffusivity (F(1,95) = 5.10, p < .006). Exploratory analyses demonstrated preliminary support for differences in visual processing networks (e.g. optic tract) as well as additional circuits less frequently examined in the context of early life adversity exposure, (e.g. corticothalamic tract).
CONCLUSIONS CONCLUSIONS
Maternal ACEs predict neural circuit development of the inferior longitudinal fasciculus. Findings suggest that early developing sensory circuits within the infant brain are susceptible to maternal adverse childhood experiences and may have implications for the maturation of higher order emotional and cognitive circuits.

Identifiants

pubmed: 39191307
pii: S0165-0327(24)01380-6
doi: 10.1016/j.jad.2024.08.146
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest CNE was an investigator for a multisite clinical trial conducted by Sage Therapeutics. She is also a consultant to EmbarkNeuro, Skyland Trail, and Health Rhythms and a member of the scientific advisory board of Babyscripts. No funding or involvement from these entities was used to support the current work, and all views expressed are solely those of the authors. All other authors have no conflicts of interest or relevant disclosures.

Auteurs

Catherine H Demers (CH)

Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States of America; Department of Psychology, University of Denver, Denver, CO, United States of America. Electronic address: catherine.demers@cuanschutz.edu.

Benjamin L Hankin (BL)

Department of Psychology, University of Illinois at Urbana-Champaign, Champaign, IL, United States of America.

Mercedes Hoeflich Haase (MH)

Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.

Erin Todd (E)

Department of Psychology, University of Denver, Denver, CO, United States of America.

M Camille Hoffman (MC)

Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States of America; Department of Obstetrics and Gynecology, Division of Maternal and Fetal Medicine, University of Colorado Denver School of Medicine, Aurora, CO, United States of America.

C Neill Epperson (CN)

Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States of America.

Martin A Styner (MA)

Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America; Department of Computer Science, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.

Elysia Poggi Davis (EP)

Department of Psychology, University of Denver, Denver, CO, United States of America; Department of Psychiatry and Human Behavior, University of California, Irvine, CA, United States of America.

Classifications MeSH