TY - JOUR
T1 - Novel gyrification networks reveal links with psychiatric risk factors in early illness
AU - Sanfelici, Rachele
AU - Ruef, Anne
AU - Antonucci, Linda A.
AU - Penzel, Nora
AU - Sotiras, Aristeidis
AU - Dong, Mark Sen
AU - Urquijo-Castro, Maria
AU - Wenzel, Julian
AU - Kambeitz-Ilankovic, Lana
AU - Hettwer, Meike D.
AU - Ruhrmann, Stephan
AU - Chisholm, Katharine
AU - Riecher-Rössler, Anita
AU - Falkai, Peter
AU - Pantelis, Christos
AU - Salokangas, Raimo K.R.
AU - Lencer, Rebekka
AU - Bertolino, Alessandro
AU - Kambeitz, Joseph
AU - Meisenzahl, Eva
AU - Borgwardt, Stefan
AU - Brambilla, Paolo
AU - Wood, Stephen J.
AU - Upthegrove, Rachel
AU - Schultze-Lutter, Frauke
AU - Koutsouleris, Nikolaos
AU - Dwyer, Dominic B.
N1 - Publisher Copyright:
© 2021 The Author(s) 2021. Published by Oxford University Press. All rights reserved.
PY - 2022/4/15
Y1 - 2022/4/15
N2 - Adult gyrification provides a window into coordinated early neurodevelopment when disruptions predispose individuals to psychiatric illness. We hypothesized that the echoes of such disruptions should be observed within structural gyrification networks in early psychiatric illness that would demonstrate associations with developmentally relevant variables rather than specific psychiatric symptoms. We employed a new data-driven method (Orthogonal Projective Non-Negative Matrix Factorization) to delineate novel gyrification-based networks of structural covariance in 308 healthy controls. Gyrification within the networks was then compared to 713 patients with recent onset psychosis or depression, and at clinical high-risk. Associations with diagnosis, symptoms, cognition, and functioning were investigated using linear models. Results demonstrated 18 novel gyrification networks in controls as verified by internal and external validation. Gyrification was reduced in patients in temporal-insular, lateral occipital, and lateral fronto-parietal networks (pFDR < 0.01) and was not moderated by illness group. Higher gyrification was associated with better cognitive performance and lifetime role functioning, but not with symptoms. The findings demonstrated that gyrification can be parsed into novel brain networks that highlight generalized illness effects linked to developmental vulnerability. When combined, our study widens the window into the etiology of psychiatric risk and its expression in adulthood.
AB - Adult gyrification provides a window into coordinated early neurodevelopment when disruptions predispose individuals to psychiatric illness. We hypothesized that the echoes of such disruptions should be observed within structural gyrification networks in early psychiatric illness that would demonstrate associations with developmentally relevant variables rather than specific psychiatric symptoms. We employed a new data-driven method (Orthogonal Projective Non-Negative Matrix Factorization) to delineate novel gyrification-based networks of structural covariance in 308 healthy controls. Gyrification within the networks was then compared to 713 patients with recent onset psychosis or depression, and at clinical high-risk. Associations with diagnosis, symptoms, cognition, and functioning were investigated using linear models. Results demonstrated 18 novel gyrification networks in controls as verified by internal and external validation. Gyrification was reduced in patients in temporal-insular, lateral occipital, and lateral fronto-parietal networks (pFDR < 0.01) and was not moderated by illness group. Higher gyrification was associated with better cognitive performance and lifetime role functioning, but not with symptoms. The findings demonstrated that gyrification can be parsed into novel brain networks that highlight generalized illness effects linked to developmental vulnerability. When combined, our study widens the window into the etiology of psychiatric risk and its expression in adulthood.
KW - clinical high risk
KW - cortical folding
KW - depression
KW - psychosis
KW - structural covariance
KW - Brain/diagnostic imaging
KW - Humans
KW - Risk Factors
KW - Adult
KW - Cerebral Cortex
KW - Magnetic Resonance Imaging/methods
KW - Psychotic Disorders/diagnostic imaging
UR - http://www.scopus.com/inward/record.url?scp=85125167416&partnerID=8YFLogxK
U2 - 10.1093/cercor/bhab288
DO - 10.1093/cercor/bhab288
M3 - Article
C2 - 34519351
AN - SCOPUS:85125167416
SN - 1047-3211
VL - 32
SP - 1625
EP - 1636
JO - Cerebral Cortex
JF - Cerebral Cortex
IS - 8
ER -