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Orbitofrontal Thickness and Network Associations as Transdiagnostic Signature of Amotivation Along the Bipolar-Schizophrenia Spectrum

Marlene Franz, Valeria Kebets, Xaver Berg, Foivos Georgiadis, Beatrice A Milano, Achim Burrer, Janis Brakowski, Stefan Kaiser, Erich Seifritz, Philipp Homan, Esther Walton, Theo G M van Erp, Jessica A Turner, Bratislav Misic, Sofie L Valk, B T Thomas Yeo, Boris C Bernhardt, Matthias Kirschner

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Abstract

BACKGROUND AND HYPOTHESIS: Negative symptoms of schizophrenia (SCZ), particularly amotivation, are prominent across both SCZ and bipolar disorder (BD). While orbitofrontal cortex (OFC) alterations have been implicated in the development of negative symptoms, their contributions across disorders remain to be established. Here, we examined how OFC thickness and network associations relate to amotivation compared to diminished expression across the BD-SCZ spectrum.

STUDY DESIGN: We included 50 individuals with SCZ, 49 with BD, and 122 controls. We assessed amotivation and diminished expression and estimated thickness in the medial and lateral OFC as regions of interest as well as 64 other cortical regions.

STUDY RESULTS: Across BD and SCZ, reduced right lateral and bilateral medial OFC thickness were specifically associated with amotivation, but not diminished expression or other clinical factors. We then generated intra-individual OFC structural covariance networks to evaluate how the system-level embedding of the OFC would link to brain-wide cortical maps of negative symptoms. We found that medial OFC covariance networks spatially correlated with the brain-wide cortical alterations of both negative symptom dimensions. Further analyses in independent SCZ data from the ENIGMA consortium (n = 4474) revealed associations with lateral OFC covariance networks. Finally, the brain-wide cortical alterations of amotivation were significantly correlated with normative functional and structural white-matter connectivity profiles of the right medial and left lateral OFC as well as adjacent prefrontal and limbic regions.

CONCLUSIONS: Our work identifies OFC alterations as a possible transdiagnostic signature of amotivation and provides insights into network associations underlying the system-wide cortical alterations of negative symptoms across SCZ and BD.

Original languageEnglish
Article numbersbaf078
JournalSchizophrenia Bulletin
Volume52
Issue number2
Early online date20 Jun 2025
DOIs
Publication statusPublished - 31 Mar 2026

Data Availability Statement

All data used in this study were derived from the UCLA CNP cohort. Data can be downloaded from the publicly available database OpenfMRI (https://openfmri.org/dataset/ds000030/).

Funding

M.K. receives funding from the Swiss Science Foundation (grant number 32003B_219240). B.T.T.Y. is supported by the NUS Yong Loo Lin School of Medicine (NUHSRO/2020/124/TMR/LOA), the Singapore National Medical Research Council (NMRC) LCG (OFLCG19May-0035), NMRC CTG-IIT (CTGIIT23jan-0001), NMRC STaR (STaR20nov-0003), Singapore Ministry of Health (MOH) Centre Grant (CG21APR1009), the Temasek Foundation (TF2223-IMH-01), and the United States National Institutes of Health (R01MH120080 and R01MH133334). E.W. receives funding from UK Research and Innovation (UKRI) under the UK government’s Horizon Europe / ERC Frontier Research Guarantee [BrainHealth, grant number EP/Y015037/1]. Research reported in this publication was supported by the National Institutes of Mental Health under Award Number R01MH121246. V.K. acknowledges postdoctoral training support by the Transforming Autism Care Consortium (TACC) and the Montreal Neurological Institute (MNI). S.L.V. was supported by the Max Planck Society, the Helmholtz International BigBrain Analytics and Learning Laboratory (Hiball), and the Jacobs foundation.

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