Neurobiological evidence of sexual dimorphism in limbic circuitry of US Veterans.


Journal

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

Informations de publication

Date de publication:
01 09 2020
Historique:
received: 09 08 2019
revised: 25 03 2020
accepted: 10 05 2020
entrez: 16 7 2020
pubmed: 16 7 2020
medline: 16 2 2021
Statut: ppublish

Résumé

Female Veterans are an increasing patient population in the Department of Veterans Affairs and may have distinct clinical and neurobiological features compared to males. Nineteen female and 19 male Veterans who met diagnostic criteria for depression/posttraumatic stress disorder (MDD/PTSD) completed diagnostic interviews, symptom measures, and resting-state neuroimaging. Participants completed clinical measures of mood and aggression in addition to magnetic resonance imaging on a 3.0 Tesla Siemens scanner. Females showed increased functional connectivity between the left and right basolateral amygdala (BLA) and the left and right cerebellar and occipital lobes. Sex differences also were evident in the relationship between affective and clinical symptoms with BLA connectivity. Females showed a correlation between revenge planning and decreased connectivity between the left BLA and left occipital lobe and also a correlation between aggression and decreased connectivity between the right BLA and right mid cingulate, right and left medial frontal lobe, and right frontal lobe. Males evidenced a relationship between increased depressive symptoms and increased connectivity between the left BLA and right and left occipital lobe, left calcarine, and other areas associated with visual memory and processing, and interpretation of sensory information. Additionally, males reported higher levels of physical aggression and revenge planning compared to females. This study included neuroimaging and self-report clinical measures. Further studies will benefit from multimodal measures, including behavioral measures of aggression. Results suggest that male Veterans report more aggression than females and symptoms of aggression and mood are differentially related to BLA connectivity by sex.

Sections du résumé

BACKGROUND
Female Veterans are an increasing patient population in the Department of Veterans Affairs and may have distinct clinical and neurobiological features compared to males.
METHODS
Nineteen female and 19 male Veterans who met diagnostic criteria for depression/posttraumatic stress disorder (MDD/PTSD) completed diagnostic interviews, symptom measures, and resting-state neuroimaging. Participants completed clinical measures of mood and aggression in addition to magnetic resonance imaging on a 3.0 Tesla Siemens scanner.
RESULTS
Females showed increased functional connectivity between the left and right basolateral amygdala (BLA) and the left and right cerebellar and occipital lobes. Sex differences also were evident in the relationship between affective and clinical symptoms with BLA connectivity. Females showed a correlation between revenge planning and decreased connectivity between the left BLA and left occipital lobe and also a correlation between aggression and decreased connectivity between the right BLA and right mid cingulate, right and left medial frontal lobe, and right frontal lobe. Males evidenced a relationship between increased depressive symptoms and increased connectivity between the left BLA and right and left occipital lobe, left calcarine, and other areas associated with visual memory and processing, and interpretation of sensory information. Additionally, males reported higher levels of physical aggression and revenge planning compared to females.
LIMITATIONS
This study included neuroimaging and self-report clinical measures. Further studies will benefit from multimodal measures, including behavioral measures of aggression.
CONCLUSIONS
Results suggest that male Veterans report more aggression than females and symptoms of aggression and mood are differentially related to BLA connectivity by sex.

Identifiants

pubmed: 32663937
pii: S0165-0327(19)32138-X
doi: 10.1016/j.jad.2020.05.016
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1091-1101

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare they have no conflicts of interest.

Auteurs

Erin McGlade (E)

Diagnostic Neuroimaging Lab, University of Utah, Salt Lake City, UT, United States; University of Utah School of Medicine, Salt Lake City, UT, United States; VISN 19 MIRREC, Salt Lake City, UT, United States. Electronic address: erin.mcglade@hsc.utah.edu.

Jadwiga Rogowska (J)

Diagnostic Neuroimaging Lab, University of Utah, Salt Lake City, UT, United States; University of Utah School of Medicine, Salt Lake City, UT, United States.

Jennifer DiMuzio (J)

Diagnostic Neuroimaging Lab, University of Utah, Salt Lake City, UT, United States; VISN 19 MIRREC, Salt Lake City, UT, United States.

Elliott Bueler (E)

Diagnostic Neuroimaging Lab, University of Utah, Salt Lake City, UT, United States; VISN 19 MIRREC, Salt Lake City, UT, United States.

Chandni Sheth (C)

Diagnostic Neuroimaging Lab, University of Utah, Salt Lake City, UT, United States; University of Utah School of Medicine, Salt Lake City, UT, United States.

Margaret Legarreta (M)

Diagnostic Neuroimaging Lab, University of Utah, Salt Lake City, UT, United States; University of Utah School of Medicine, Salt Lake City, UT, United States; VISN 19 MIRREC, Salt Lake City, UT, United States.

Deborah Yurgelun-Todd (D)

Diagnostic Neuroimaging Lab, University of Utah, Salt Lake City, UT, United States; University of Utah School of Medicine, Salt Lake City, UT, United States; VISN 19 MIRREC, Salt Lake City, UT, United States.

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Classifications MeSH