Neural Substrates of Psychotic Depression: Findings from the Global ECT-MRI Research Collaboration

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Dokumenter

  • Fulltext

    Forlagets udgivne version, 21,7 MB, PDF-dokument

  • Akihiro Takamiya
  • Annemiek Dols
  • Louise Emsell
  • Christopher Abbott
  • Antoine Yrondi
  • Carles Soriano Mas
  • Pia Nordanskog
  • Didi Rhebergen
  • Eric Van Exel
  • Mardien L. Oudega
  • Filip Bouckaert
  • Mathieu Vandenbulcke
  • Pascal Sienaert
  • Patrice Peran
  • Marta Cano
  • Narcis Cardoner
  • Paul Hamilton
  • Robin Kampe
  • Willem Bruin
  • Hauke Bartsch
  • Olga Therese Ousdal
  • Ute Kessler
  • Guido Van Wingen
  • Leif Oltedal
  • Taishiro Kishimoto

Psychotic major depression (PMD) is hypothesized to be a distinct clinical entity from nonpsychotic major depression (NPMD). However, neurobiological evidence supporting this notion is scarce. The aim of this study is to identify gray matter volume (GMV) differences between PMD and NPMD and their longitudinal change following electroconvulsive therapy (ECT). Structural magnetic resonance imaging (MRI) data from 8 independent sites in the Global ECT-MRI Research Collaboration (GEMRIC) database (n = 108; 56 PMD and 52 NPMD; mean age 71.7 in PMD and 70.2 in NPMD) were analyzed. All participants underwent MRI before and after ECT. First, cross-sectional whole-brain voxel-wise GMV comparisons between PMD and NPMD were conducted at both time points. Second, in a flexible factorial model, a main effect of time and a group-by-time interaction were examined to identify longitudinal effects of ECT on GMV and longitudinal differential effects of ECT between PMD and NPMD, respectively. Compared with NPMD, PMD showed lower GMV in the prefrontal, temporal and parietal cortex before ECT; PMD showed lower GMV in the medial prefrontal cortex (MPFC) after ECT. Although there was a significant main effect of time on GMV in several brain regions in both PMD and NPMD, there was no significant group-by-time interaction. Lower GMV in the MPFC was consistently identified in PMD, suggesting this may be a trait-like neural substrate of PMD. Longitudinal effect of ECT on GMV may not explain superior ECT response in PMD, and further investigation is needed.

OriginalsprogEngelsk
TidsskriftSchizophrenia Bulletin
Vol/bind48
Udgave nummer2
Sider (fra-til)514-523
Antal sider10
ISSN0586-7614
DOI
StatusUdgivet - 2022

Bibliografisk note

Publisher Copyright:
© 2021 The Author(s). Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center.

ID: 310433287