English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Coordinated cortical thickness alterations across six neurodevelopmental and psychiatric disorders

MPS-Authors
/persons/resource/persons270685

Hettwer,  Meike
Otto Hahn Group Cognitive Neurogenetics, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

/persons/resource/persons71665

Valk,  Sofie L.       
Otto Hahn Group Cognitive Neurogenetics, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

Hettwer_2022.pdf
(Publisher version), 3MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Hettwer, M., Larivière, S., Park, B. Y., van den Heuvel, O. A., Schmaal, L., Andreassen, O. A., et al. (2022). Coordinated cortical thickness alterations across six neurodevelopmental and psychiatric disorders. Nature Communications, 13: 6851. doi:10.1038/s41467-022-34367-6.


Cite as: https://hdl.handle.net/21.11116/0000-000B-758C-4
Abstract
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.