Adverse Childhood Experiences and Amygdalar Reduction: High-Resolution Segmentation Reveals Associations With Subnuclei and Psychiatric Outcomes.


Journal

Child maltreatment
ISSN: 1552-6119
Titre abrégé: Child Maltreat
Pays: United States
ID NLM: 9602869

Informations de publication

Date de publication:
11 2019
Historique:
pubmed: 30 4 2019
medline: 29 9 2020
entrez: 30 4 2019
Statut: ppublish

Résumé

The aim of the present study was 2-fold: (1) to utilize improved amygdala segmentation and exploratory factor analysis to characterize the latent volumetric structure among amygdala nuclei and (2) to assess the effect of adverse childhood experiences (ACEs) on amygdalar morphometry and current psychiatric symptoms. To investigate these aims, structural (T1) MRI and self-report data were obtained from 119 emerging adults. Regression analysis showed that higher ACE scores were related to reduced volume of the right, but not the left, amygdalar segments. Further, exploratory factor analysis yielded a two-factor structure, basolateral and central-medial nuclei of the right amygdala. Stractual equation modeling analyses revealed that higher ACE scores were significantly related to a reduced volume of the right basolateral and central-medial segments. Furthermore, reduction in the right basolateral amygdala was associated with increased anxiety, depressive symptoms, and alcohol use. This association supports an indirect effect between early adversity and psychiatric problems via reduced right basolateral amygdalar volume. The high-resolution segmentation results reveal a latent structure among amygdalar nuclei, which is consistent with prior work conducted in nonhuman mammals. These findings extend previous reports linking early adversity, right amygdala volume, and psychopathology.

Identifiants

pubmed: 31030539
doi: 10.1177/1077559519839491
pmc: PMC6813855
mid: NIHMS1028617
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

400-410

Subventions

Organisme : NIDA NIH HHS
ID : K01 DA045219
Pays : United States
Organisme : NIDA NIH HHS
ID : P30 DA027827
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Assaf Oshri (A)

Department of Human Development and Family Science, The Youth Development Institute, University of Georgia, Athens, GA, USA.
Department of Psychology, University of Georgia, Athens, GA, USA.

Joshua C Gray (JC)

Department of Medical and Clinical Psychology, Uniformed Services University, Bethesda, MD, USA.

Max M Owens (MM)

Department of Psychology, University of Georgia, Athens, GA, USA.

Sihong Liu (S)

Department of Human Development and Family Science, The Youth Development Institute, University of Georgia, Athens, GA, USA.

Erinn Bernstein Duprey (EB)

Department of Human Development and Family Science, The Youth Development Institute, University of Georgia, Athens, GA, USA.

Lawrence H Sweet (LH)

Department of Psychology, University of Georgia, Athens, GA, USA.
Department of Psychiatry and Human Behavior, Alpert Medical School of Brown University, Providence, RI, USA.

James MacKillop (J)

Peter Boris Centre for Addictions Research, McMaster University/St. Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

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Classifications MeSH