TY - JOUR
T1 - Sex Differences in Lifespan Trajectories and Variability of Human Sulcal and Gyral Morphology
AU - Díaz-Caneja, Covadonga M
AU - Alloza, Clara
AU - Gordaliza, Pedro M
AU - Fernández-Pena, Alberto
AU - de Hoyos, Lucía
AU - Santonja, Javier
AU - Buimer, Elizabeth E L
AU - van Haren, Neeltje E M
AU - Cahn, Wiepke
AU - Arango, Celso
AU - Kahn, René S
AU - Hulshoff Pol, Hilleke E
AU - Schnack, Hugo G
AU - Janssen, Joost
N1 - Publisher Copyright:
© 2021 The Author(s) 2021. Published by Oxford University Press. All rights reserved.
PY - 2021/11/1
Y1 - 2021/11/1
N2 - Sex differences in the development and aging of human sulcal morphology have been understudied. We charted sex differences in trajectories and inter-individual variability of global sulcal depth, width, and length, pial surface area, exposed (hull) gyral surface area, unexposed sulcal surface area, cortical thickness, gyral span, and cortex volume across the lifespan in a longitudinal sample (700 scans, 194 participants 2 scans, 104 three scans, age range: 16-70 years) of neurotypical males and females. After adjusting for brain volume, females had thicker cortex and steeper thickness decline until age 40 years; trajectories converged thereafter. Across sexes, sulcal shortening was faster before age 40, while sulcal shallowing and widening were faster thereafter. Although hull area remained stable, sulcal surface area declined and was more strongly associated with sulcal shortening than with sulcal shallowing and widening. Males showed greater variability for cortex volume and lower variability for sulcal width. Our findings highlight the association between loss of sulcal area, notably through sulcal shortening, with cortex volume loss. Studying sex differences in lifespan trajectories may improve knowledge of individual differences in brain development and the pathophysiology of neuropsychiatric conditions.
AB - Sex differences in the development and aging of human sulcal morphology have been understudied. We charted sex differences in trajectories and inter-individual variability of global sulcal depth, width, and length, pial surface area, exposed (hull) gyral surface area, unexposed sulcal surface area, cortical thickness, gyral span, and cortex volume across the lifespan in a longitudinal sample (700 scans, 194 participants 2 scans, 104 three scans, age range: 16-70 years) of neurotypical males and females. After adjusting for brain volume, females had thicker cortex and steeper thickness decline until age 40 years; trajectories converged thereafter. Across sexes, sulcal shortening was faster before age 40, while sulcal shallowing and widening were faster thereafter. Although hull area remained stable, sulcal surface area declined and was more strongly associated with sulcal shortening than with sulcal shallowing and widening. Males showed greater variability for cortex volume and lower variability for sulcal width. Our findings highlight the association between loss of sulcal area, notably through sulcal shortening, with cortex volume loss. Studying sex differences in lifespan trajectories may improve knowledge of individual differences in brain development and the pathophysiology of neuropsychiatric conditions.
KW - brain aging
KW - brain development
KW - gyral
KW - sexual dimorphism
KW - sulcal
UR - http://www.scopus.com/inward/record.url?scp=85118096222&partnerID=8YFLogxK
U2 - 10.1093/cercor/bhab145
DO - 10.1093/cercor/bhab145
M3 - Article
C2 - 34179960
SN - 1047-3211
VL - 31
SP - 5107
EP - 5120
JO - Cerebral Cortex
JF - Cerebral Cortex
IS - 11
ER -