A1 Refereed original research article in a scientific journal

Exploring the predictive value of structural covariance networks for the diagnosis of schizophrenia




AuthorsVetter, Clara S.; Bender, Annika; Dwyer, Dominic B.; Montembeault, Max; Ruef, Anne; Chisholm, Katharine; Kambeitz-Ilankovic, Lana; Antonucci, Linda A.; Ruhrmann, Stephan; Kambeitz, Joseph; Rosen, Marlene; Lichtenstein, Theresa; Riecher-Rossler, Anita; Upthegrove, Rachel; Salokangas, Raimo K. R.; Hietala, Jarmo; Pantelis, Christos; Lencer, Rebekka; Meisenzahl, Eva; Wood, Stephen J.; Brambilla, Paolo; Borgwardt, Stefan; Falkai, Peter; Bertolino, Alessandro; Koutsouleris, Nikolaos; PRONIA Consortium

PublisherFRONTIERS MEDIA SA

Publishing placeLAUSANNE

Publication year2025

JournalFrontiers in Psychiatry

Journal name in sourceFRONTIERS IN PSYCHIATRY

Journal acronymFRONT PSYCHIATRY

Article number1570797

Volume16

Number of pages15

eISSN1664-0640

DOIhttps://doi.org/10.3389/fpsyt.2025.1570797

Web address https://doi.org/10.3389/fpsyt.2025.1570797

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/499178940


Abstract

Introduction
Schizophrenia is a psychiatric disorder hypothesized to result from disturbed brain connectivity. Structural covariance networks (SCN) describe the shared variation in morphological properties emerging from coordinated neurodevelopmental processes, This study evaluates the potential of SCNs as diagnostic biomarker for schizophrenia.

Methods
We compared the diagnostic value of two SCN computation methods derived from regional gray matter volume (GMV) in 154 patients with a diagnosis of first episode psychosis or recurrent schizophrenia (PAT) and 366 healthy control individuals (HC). The first method (REF-SCN) quantifies the contribution of an individual to a normative reference group's SCN, and the second approach (KLS-SCN) uses a symmetric version of Kulback-Leibler divergence. Their diagnostic value compared to regional GMV was assessed in a stepwise analysis using a series of linear support vector machines within a nested cross-validation framework and stacked generalization, all models were externally validated in an independent sample (NPAT=71, NHC=74), SCN feature importance was assessed, and the derived risk scores were analyzed for differential relationships with clinical variables.

Results
We found that models trained on SCNs were able to classify patients with schizophrenia and combining SCNs and regional GMV in a stacked model improved training (balanced accuracy (BAC)=69.96%) and external validation performance (BAC=67.10%). Among all unimodal models, the highest discovery sample performance was achieved by a model trained on REF-SCN (balanced accuracy (BAC=67.03%). All model decisions were driven by widespread structural covariance alterations involving the somato-motor, default mode, control, visual, and the ventral attention networks. Risk estimates derived from KLS-SCNs and regional GMV, but not REF-SCNs, could be predicted from clinical variables, especially driven by body mass index (BMI) and affect-related negative symptoms.

Discussion
These patterns of results show that different SCN computation approaches capture different aspects of the disease. While REF-SCNs contain valuable information for discriminating schizophrenia from healthy control individuals, KLS-SCNs may capture more nuanced symptom-level characteristics similar to those captured by PCA of regional GMV.


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Funding information in the publication
The author(s) declare that financial support was received for the research and/or publication of this article. PRONIA is a Collaboration Project funded by the European Union under the 7th Framework Programme under grant agreement n° 602152. NK is supported through grants from NIH (U01MH124639-01; ProNET), the Wellcome Trust, the German Innovation Fund (CARE project), the German Federal Ministry of Education and Research (COMMITMENT and BEST projects), as well as ERA PerMed (IMPLEMENT project). DP was supported by the Else-Kröner-Fresenius-Foundation through the Clinician Scientist Program ‘EKFS-Translational Psychiatry’.


Last updated on 2025-15-08 at 11:04