Trait-related changes in brain network topology in premenstrual dysphoric disorder.


Journal

Hormones and behavior
ISSN: 1095-6867
Titre abrégé: Horm Behav
Pays: United States
ID NLM: 0217764

Informations de publication

Date de publication:
08 2020
Historique:
received: 02 02 2020
revised: 26 04 2020
accepted: 22 05 2020
pubmed: 30 5 2020
medline: 29 4 2021
entrez: 30 5 2020
Statut: ppublish

Résumé

The female predominance in the prevalence of depression is partially accounted by reactivity to hormonal fluctuations. Premenstrual dysphoric disorder (PMDD) is a reproductive subtype of depression characterized by cyclic emotional and somatic symptoms that recur before menstruation. Despite the growing understanding that most psychiatric disorders arise from dysfunctions in distributed brain circuits, the brain's functional connectome and its network properties of segregation and integration were not investigated in PMDD. To this end, we examined the brain's functional network organization in PMDD using graph theoretical analysis. 24 drug naïve women with PMDD and 27 controls without premenstrual symptoms underwent 2 resting-state fMRI scans, during the mid-follicular and late-luteal menstrual cycle phases. Functional connectivity MRI, graph theory metrics, and levels of sex hormones were computed during each menstrual phase. Altered network topology was found in PMDD across symptomatic and remitted stages in major graph metrics (characteristic path length, clustering coefficient, transitivity, local and global efficiency, centrality), indicating decreased functional network segregation and increased functional network integration. In addition, PMDD patients exhibited hypoconnectivity of the anterior temporal lobe and hyperconnectivity of the basal ganglia and thalamus, across menstrual phases. Furthermore, the relationship between difficulties in emotion regulation and PMDD was mediated by specific patterns of functional connectivity, including connections of the striatum, thalamus, and prefrontal cortex. The shifts in the functional connectome and its topology in PMDD may suggest trait vulnerability markers of the disorder.

Identifiants

pubmed: 32470339
pii: S0018-506X(20)30108-2
doi: 10.1016/j.yhbeh.2020.104782
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104782

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest.

Auteurs

Rotem Dan (R)

Edmond and Lily Safra Center for Brain Sciences (ELSC), The Hebrew University of Jerusalem, Jerusalem, Israel; Department of Neurology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

Inbal Reuveni (I)

Department of Psychiatry, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

Laura Canetti (L)

Department of Psychiatry, Hadassah Hebrew University Medical Center, Jerusalem, Israel; Department of Psychology, The Hebrew University of Jerusalem, Jerusalem, Israel.

Marta Weinstock (M)

Institute of Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel.

Ronen Segman (R)

Department of Psychiatry, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

Gadi Goelman (G)

Department of Neurology, Hadassah Hebrew University Medical Center, Jerusalem, Israel. Electronic address: gadig@hadassah.org.il.

Omer Bonne (O)

Department of Psychiatry, Hadassah Hebrew University Medical Center, Jerusalem, Israel.

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Classifications MeSH