Associations of lesion location, structural disconnection, and functional diaschisis with depressive symptoms post stroke.

depression diaschisis disconnection lesion network mapping stroke

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2023
Historique:
received: 14 01 2023
accepted: 20 04 2023
medline: 2 6 2023
pubmed: 2 6 2023
entrez: 2 6 2023
Statut: epublish

Résumé

Post-stroke depressive symptoms (PSDS) are common and relevant for patient outcome, but their complex pathophysiology is ill understood. It likely involves social, psychological and biological factors. Lesion location is a readily available information in stroke patients, but it is unclear if the neurobiological substrates of PSDS are spatially localized. Building on previous analyses, we sought to determine if PSDS are associated with specific lesion locations, structural disconnection and/or localized functional diaschisis. In a prospective observational study, we examined 270 patients with first-ever stroke with the Hospital Anxiety and Depression Scale (HADS) around 6 months post-stroke. Based on individual lesion locations and the depression subscale of the HADS we performed support vector regression lesion-symptom mapping, structural-disconnection-symptom mapping and functional lesion network-symptom-mapping, in a reanalysis of this previously published cohort to infer structure-function relationships. We found that depressive symptoms were associated with (i) lesions in the right insula, right putamen, inferior frontal gyrus and right amygdala and (ii) structural disconnection in the right temporal lobe. In contrast, we found no association with localized functional diaschisis. In addition, we were unable to confirm a previously described association between depressive symptom load and a network damage score derived from functional disconnection maps. Based on our results, and other recent lesion studies, we see growing evidence for a prominent role of right frontostriatal brain circuits in PSDS.

Identifiants

pubmed: 37265471
doi: 10.3389/fneur.2023.1144228
pmc: PMC10231644
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1144228

Informations de copyright

Copyright © 2023 Klingbeil, Brandt, Stockert, Baum, Hoffmann, Saur and Wawrzyniak.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Julian Klingbeil (J)

Neuroimaging Laboratory, Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Max-Lennart Brandt (ML)

Neuroimaging Laboratory, Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Anika Stockert (A)

Neuroimaging Laboratory, Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Petra Baum (P)

Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Karl-Titus Hoffmann (KT)

Department of Neuroradiology, University of Leipzig Medical Center, Leipzig, Germany.

Dorothee Saur (D)

Neuroimaging Laboratory, Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Max Wawrzyniak (M)

Neuroimaging Laboratory, Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Classifications MeSH