# Normative age-related structural brain deviations underlying psychopathology, cognitive impairment and neurological soft signs in schizophrenia spectrum disorders

**Authors:** Sebastian Volkmer, Katharina M. Kubera, Stefan Fritze, Geva Brandt, Dilsa Cemre Akkoc Altinok, Jonas Daub, Jacqueline Kukovic, Kent-Tjorben Böttcher, Oksana Berhe, Yuchen Lin, Heike Tost, Andre F. Marquand, Andreas Meyer-Lindenberg, Emanuel Schwarz, Dusan Hirjak

PMC · DOI: 10.1038/s41398-026-03956-0 · Translational Psychiatry · 2026-03-20

## TL;DR

This study shows that brain structure deviations in schizophrenia spectrum disorders are linked to cognitive and behavioral symptoms, using a large-scale model to identify patterns across different sites.

## Contribution

The study demonstrates that normative modeling features from a large healthy dataset can generalize and reveal brain-behavior associations in schizophrenia.

## Key findings

- A random forest classifier achieved 65% balanced accuracy in classifying schizophrenia spectrum disorder cases.
- Structural deviations in limbic and sensorimotor regions were strongly linked to cognitive impairment and neurological soft signs.
- NM features from a large external reference showed robust multivariate relationships with clinical outcomes in SSD.

## Abstract

Schizophrenia spectrum disorders (SSD) are marked by widespread structural brain abnormalities. Neuroanatomical normative modeling (NM) can quantify person-specific deviations from healthy variability, yet it remains unknown whether pre-trained, large-scale NM features support site-held-out classification and mechanistic brain–behavior mapping in SSD. Here, we applied a publicly available PCNtoolkit model (trained on ~57,000 healthy controls from 82 sites) to six independent cohorts (N = 831) to derive individual deviations in cortical thickness (CT) and subcortical volumes from T1-weighted MRI. Employing a random forest classifier with leave-site-out cross-validation, we achieved a balanced accuracy of 65%, which underscores the inherent complexity of SSD. Feature importance analysis identified total gray matter volume, mean CT, and CT changes in limbic and sensorimotor regions as key predictive features. Relative to healthy controls, SSD participants showed a higher burden of extreme negative deviations, which related to reduced attention and processing speed and to elevated neurological soft signs (NSS). Finally, canonical correlation analysis revealed a robust multivariate relationship linking structural deviationsparticularly CT changes in limbic and sensorimotor cortices, to cognition and NSS. Together, these results demonstrate that NM features transferred from a large external reference can generalize across sites and elucidate clinically relevant brain–behavior associations in SSD, supporting the integration of multimodal, large-scale datasets to advance biomarker discovery and inform earlier, more targeted interventions.

## Full-text entities

- **Genes:** AGER (advanced glycosylation end-product specific receptor) [NCBI Gene 177] {aka RAGE, SCARJ1, sRAGE}, TPSG1 (tryptase gamma 1) [NCBI Gene 25823] {aka PRSS31, TMT, trpA}, MAFD2 (major affective disorder 2) [NCBI Gene 4096] {aka BPAD, MDI, MDX}, COMT (catechol-O-methyltransferase) [NCBI Gene 1312] {aka HEL-S-98n}
- **Diseases:** SSD (MESH:D019967), ventricular enlargement (MESH:D006332), dyskinesia (MESH:D004409), Negative Syndrome (MESH:D064726), structural abnormalities (MESH:C566527), schizophrenia (MESH:D012559), DSM-IV Axis I and II Disorders (MESH:C566610), RDoC (MESH:D014947), HC (MESH:D000067329), neurodegeneration (MESH:D019636), loss of consciousness (MESH:D014474), NM (MESH:D004195), neurodevelopmental disturbances (MESH:D014832), RLSPO (MESH:D016773), psychotic disorders (MESH:D011618), mental retardation (MESH:D008607), pain (MESH:D010146), substance abuse (MESH:D019966), mental disorders (MESH:D001523), cognitive and sensorimotor dysfunction (MESH:D003072), dilation of the lateral ventricles (MESH:D002311), brain disorders (MESH:D001927), SCID (MESH:D053632), bipolar disorder (MESH:D001714), sensorimotor abnormalities (MESH:D020233), motor coordination deficits (MESH:D001259), sensori- (MESH:D009477), ASD (MESH:D000067877), Positive (MESH:D000377), DSM Disorders (MESH:D009358), dementia (MESH:D003704), head trauma (MESH:D006259), catatonia (MESH:D002389), gesture impairments (MESH:D001072), major depression (MESH:D003865), ADHD (MESH:D001289), psychomotor abnormalities (MESH:D011596), NSS (MESH:D009461)
- **Chemicals:** DSST (-), MP (MESH:C063925)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13039878/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC13039878/full.md

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Source: https://tomesphere.com/paper/PMC13039878