TY - JOUR
T1 - Congenital blindness is associated with large-scale reorganization of anatomical networks
AU - Hasson, Uri
AU - Andric, Michael
AU - Atilgan, Hicret
AU - Collignon, Olivier
N1 - Funding Information:
This project was supported by European Research Council Starting Grants: ERC-STG #263318 NeuroInt to U.H., and ERC-STG #337573 MADVIS to O.C, the Fond de Recherches en Santé du Québec, and the Canadian Institutes of Health Research. The data were collected while O.C was a post-doctoral fellow with Dr. Franco Lepore, and we thank Dr. Lepore for allowing us to use these data. We also thank Giulia Dormal, Latifa Lazzouni, Maxime Pelland, and the UNF (Unité de Neuroimagerie Fonctionelle) team of the Research Center at the Geriatric Institute of the University of Montreal for their invaluable help in collecting these data, and the Institut Nazareth et Louis Braille of Montreal for their help in recruiting the blind participants.
Publisher Copyright:
© 2015 The Authors.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Blindness is a unique model for understanding the role of experience in the development of the brain's functional and anatomical architecture. Documenting changes in the structure of anatomical networks for this population would substantiate the notion that the brain's core network-level organization may undergo neuroplasticity as a result of life-long experience. To examine this issue, we compared whole-brain networks of regional cortical-thickness covariance in early blind and matched sighted individuals. This covariance is thought to reflect signatures of integration between systems involved in similar perceptual/cognitive functions. Using graph-theoretic metrics, we identified a unique mode of anatomical reorganization in the blind that differed from that found for sighted. This was seen in that network partition structures derived from subgroups of blind were more similar to each other than they were to partitions derived from sighted. Notably, after deriving network partitions, we found that language and visual regions tended to reside within separate modules in sighted but showed a pattern of merging into shared modules in the blind. Our study demonstrates that early visual deprivation triggers a systematic large-scale reorganization of whole-brain cortical-thickness networks, suggesting changes in how occipital regions interface with other functional networks in the congenitally blind.
AB - Blindness is a unique model for understanding the role of experience in the development of the brain's functional and anatomical architecture. Documenting changes in the structure of anatomical networks for this population would substantiate the notion that the brain's core network-level organization may undergo neuroplasticity as a result of life-long experience. To examine this issue, we compared whole-brain networks of regional cortical-thickness covariance in early blind and matched sighted individuals. This covariance is thought to reflect signatures of integration between systems involved in similar perceptual/cognitive functions. Using graph-theoretic metrics, we identified a unique mode of anatomical reorganization in the blind that differed from that found for sighted. This was seen in that network partition structures derived from subgroups of blind were more similar to each other than they were to partitions derived from sighted. Notably, after deriving network partitions, we found that language and visual regions tended to reside within separate modules in sighted but showed a pattern of merging into shared modules in the blind. Our study demonstrates that early visual deprivation triggers a systematic large-scale reorganization of whole-brain cortical-thickness networks, suggesting changes in how occipital regions interface with other functional networks in the congenitally blind.
UR - http://www.scopus.com/inward/record.url?scp=84955162843&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84955162843&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2015.12.048
DO - 10.1016/j.neuroimage.2015.12.048
M3 - Article
C2 - 26767944
AN - SCOPUS:84955162843
SN - 1053-8119
VL - 128
SP - 362
EP - 372
JO - NeuroImage
JF - NeuroImage
ER -