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Maternal adverse childhood experiences and infant subcortical brain volume.
Demers, Catherine H; Hankin, Benjamin L; Hennessey, Ella-Marie P; Haase, Mercedes Hoeflich; Bagonis, Maria M; Kim, Sun Hyung; Gilmore, John H; Hoffman, M Camille; Styner, Martin A; Davis, Elysia Poggi.
Afiliação
  • Demers CH; Department of Psychology, University of Denver, Denver, CO, USA.
  • Hankin BL; Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Hennessey EP; Department of Psychology, University of Illinois at Urbana-Champaign, Champaign, IL, USA.
  • Haase MH; Department of Psychology, University of Denver, Denver, CO, USA.
  • Bagonis MM; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Kim SH; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Gilmore JH; PrimeNeuro, Durham, NC, USA.
  • Hoffman MC; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Styner MA; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Davis EP; Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Neurobiol Stress ; 21: 100487, 2022 Nov.
Article em En | MEDLINE | ID: mdl-36532374
ABSTRACT

Background:

A large body of research supports the deleterious effects of adverse childhood experiences (ACEs) on disease susceptibility and health for both the exposed individual and the next generation. It is likely that there is an intergenerational transmission of risk from mother to child; however, the mechanisms through which such risk is conferred remain unknown. The current study evaluated the association between maternal ACEs, neonatal brain development of the amygdala and hippocampus, and later infant negative emotionality at six months of age.

Methods:

The sample included 85 mother-infant dyads (44 female infants) from a longitudinal study. Maternal ACEs were assessed with the Adverse Childhood Experiences Questionnaire (ACE-Q) and neonatal hippocampal and amygdala volume was assessed using structural magnetic resonance imaging (MRI). Infant negative emotionality was assessed at 6 months using the Infant Behavior Questionnaire (IBQ).

Results:

Multivariate analyses demonstrated that maternal ACEs were associated with bilateral amygdala volume (F(2,78) = 3.697,p = .029). Specifically, higher maternal ACEs were associated with smaller left (ß = -0.220, t(79) = -2.661, p = .009, R2 = 0.494, and right (ß = -0.167, t(79) = -2.043, p = .044, R2 = 0.501) amygdala volume. No significant association between maternal ACEs and bilateral hippocampal volume (F(2,78) = 0.215,p = .0807) was found. Follow-up regression analyses demonstrated that both high maternal ACEs and smaller left amygdala volume were associated with higher infant negative emotionality at six months of age (ß = .232, p = .040, R2 = 0.094, and ß = -0.337, p = .022, R2 = 0.16, respectively) although statistically significant mediation of this effect was not observed (Indirect effect = 0.0187, 95% CI [-0.0016-0.0557]).

Conclusions:

Maternal ACEs are associated with both newborn amygdala volume and subsequent infant negative emotionality. These findings linking maternal adverse childhood experiences and infant brain development and temperament provide evidence to support the intergenerational transmission of adversity from mother to child.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article