The individuality of shape asymmetries of the human cerebral cortex

Journal article


Chen, Yu-Chi, Arnatkevičiūtė, Aurina, McTavish, Eugene, Pang, James C., Chopra, Sidhant, Suo, Chao, Fornito, Alex and Aquino, Kevin M.. (2022). The individuality of shape asymmetries of the human cerebral cortex. eLife. 11, p. Article e75056. https://doi.org/10.7554/eLife.75056
AuthorsChen, Yu-Chi, Arnatkevičiūtė, Aurina, McTavish, Eugene, Pang, James C., Chopra, Sidhant, Suo, Chao, Fornito, Alex and Aquino, Kevin M.
Abstract

Asymmetries of the cerebral cortex are found across diverse phyla and are particularly pronounced in humans, with important implications for brain function and disease. However, many prior studies have confounded asymmetries due to size with those due to shape. Here, we introduce a novel approach to characterize asymmetries of the whole cortical shape, independent of size, across different spatial frequencies using magnetic resonance imaging data in three independent datasets. We find that cortical shape asymmetry is highly individualized and robust, akin to a cortical fingerprint, and identifies individuals more accurately than size-based descriptors, such as cortical thickness and surface area, or measures of inter-regional functional coupling of brain activity. Individual identifiability is optimal at coarse spatial scales (~37 mm wavelength), and shape asymmetries show scale-specific associations with sex and cognition, but not handedness. While unihemispheric cortical shape shows significant heritability at coarse scales (~65 mm wavelength), shape asymmetries are determined primarily by subject-specific environmental effects. Thus, coarse-scale shape asymmetries are highly personalized, sexually dimorphic, linked to individual differences in cognition, and are primarily driven by stochastic environmental influences.

Year2022
JournaleLife
Journal citation11, p. Article e75056
PublishereLife Sciences Publications Ltd
ISSN2050-084X
Digital Object Identifier (DOI)https://doi.org/10.7554/eLife.75056
PubMed ID36197720
Scopus EID2-s2.0-85141473253
PubMed Central IDPMC9668337
Open accessPublished as ‘gold’ (paid) open access
Page range1-28
FunderSylvia and Charles Viertel Charitable Foundation
National Health and Medical Research Council (NHMRC)
Australian Research Council (ARC)
Publisher's version
License
File Access Level
Open
Output statusPublished
Publication dates
Online05 Oct 2022
Publication process dates
Accepted04 Oct 2022
Deposited07 Aug 2023
ARC Funded ResearchThis output has been funded, wholly or partially, under the Australian Research Council Act 2001
Grant ID1197431
1146292
DP200103509
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