Coordinated cortical thickness alterations across six neurodevelopmental and psychiatric disorders

Neuropsychiatric disorders are increasingly conceptualized as overlapping spectra sharing multi-level neurobiological alterations. However, whether transdiagnostic cortical alterations covary in a biologically meaningful way is currently unknown. Here, we studied co-alteration networks across six ne...

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Published inNature communications Vol. 13; no. 1; pp. 6851 - 14
Main Authors Hettwer, M. D., Larivière, S., Park, B. Y., van den Heuvel, O. A., Schmaal, L., Andreassen, O. A., Ching, C. R. K., Hoogman, M., Buitelaar, J., van Rooij, D., Veltman, D. J., Stein, D. J., Franke, B., van Erp, T. G. M., Jahanshad, N., Thompson, P. M., Thomopoulos, S. I., Bethlehem, R. A. I., Bernhardt, B. C., Eickhoff, S. B., Valk, S. L.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 11.11.2022
Nature Publishing Group
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ISSN2041-1723
2041-1723
DOI10.1038/s41467-022-34367-6

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Summary:Neuropsychiatric disorders are increasingly conceptualized as overlapping spectra sharing multi-level neurobiological alterations. However, whether transdiagnostic cortical alterations covary in a biologically meaningful way is currently unknown. Here, we studied co-alteration networks across six neurodevelopmental and psychiatric disorders, reflecting pathological structural covariance. In 12,024 patients and 18,969 controls from the ENIGMA consortium, we observed that co-alteration patterns followed normative connectome organization and were anchored to prefrontal and temporal disease epicenters. Manifold learning revealed frontal-to-temporal and sensory/limbic-to-occipitoparietal transdiagnostic gradients, differentiating shared illness effects on cortical thickness along these axes. The principal gradient aligned with a normative cortical thickness covariance gradient and established a transcriptomic link to cortico-cerebello-thalamic circuits. Moreover, transdiagnostic gradients segregated functional networks involved in basic sensory, attentional/perceptual, and domain-general cognitive processes, and distinguished between regional cytoarchitectonic profiles. Together, our findings indicate that shared illness effects occur in a synchronized fashion and along multiple levels of hierarchical cortical organization. Neuropsychiatric disorders may have shared features. Here the authors identified hubs of transdiagnostic co-alteration networks using meta-analytical maps of ENIGMA neuroimaging data for six neurodevelopmental and psychiatric disorders.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-022-34367-6