- Autoencoder-based normative modelling of MRI in ~54,000 participants quantified individual deviations in brain structure across depressive, anxiety and alcohol-use symptom dimensions.
- Deviation magnitude rose with depression and anxiety severity, was greatest with high alcohol use, and shared depression-anxiety patterns generalised across cohorts.
- Distributed regional deviation patterns improved classification of symptomatic status beyond demographics, supporting reproducible, dimensional and transdiagnostic models of internalising psychopathology.
Mol Psychiatry. 2026 Jul 18. doi: 10.1038/s41380-026-03691-4. Online ahead of print.
ABSTRACT
Structural brain alterations associated with depression and anxiety are subtle, heterogeneous, and difficult to characterize. We applied autoencoder-based normative modeling to contrastively learned structural MRI representations from two large population-based cohorts (German National Cohort, N ≈ 29,000; UK Biobank, N ≈ 25,000) to quantify individual deviations from normative brain structure across symptom dimensions of depression, anxiety, and, for contextualization, alcohol use.Deviation magnitude increased with symptom severity for depressive and anxiety symptoms and was most pronounced in individuals with high alcohol use. Directional analyses revealed shared deviation patterns for depression and anxiety that were largely distinct from alcohol-related deviations, and these patterns generalized across cohorts. These affective-symptom-related patterns implicated distributed regional brain-structural variation. Individual deviation profiles improved classification of symptomatic status beyond demographic covariates, with gains concentrated at higher symptom severity.Together, these findings indicate that affective symptoms are associated with reproducible, dimensional patterns of regional brain-structural deviation that extend beyond normative population variability, supporting transdiagnostic models of internalizing psychopathology.
PMID:42471446 | DOI:10.1038/s41380-026-03691-4
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