bioRxivNeurosciencePreprint
Charting structural brain asymmetry across the human lifespan
Lena DorfschmidtiD, Simon Richard WhiteiD, Margaret GardneriD, Saashi A. BedfordiD, Gareth BalliD, Anthony David EdwardsiD, Yuanjun GuiD, Yuankai HeiD, Hao HuangiD, Shivaram KarandikariD, Vanessa KyriakopoulouiD, Minhui Ouyuang, Elmo P. PulliiD, Armin RaznahaniD, Emma C. RobinsoniD, Rafael Romero-GarcíaiD, Theodore Daniel SatterthwaiteiD, Jenna SchabdachiD, Isaac SebeniusiD, Zhiqiang ShaiD, Russell Taki ShinoharaiD, Jetro J. TuulariiD, Matilde Maria Serena VaghiiD, Jacob W. VogeliD, František VášaiD, , Aaron F. Alexander‐BlochiD
Abstract
Lateralization is a fundamental principle of structural brain organization. In vivo imaging of brain asymmetry is essential for deciphering lateralized brain functions and their disruption in neurodevelopmental and neurodegenerative disorders. Here, we present a normative framework for benchmarking brain asymmetry across the lifespan, developed from an aggregated sample of 128 primary neuroimaging studies, including 177,701 scans from 138,231 individuals, jointly spanning the age range from 20 post menstrual weeks to 102 years. This resource includes comprehensive, hemisphere-specific brain growth charts for multiple neuroimaging phenotypes: regional cortical grey matter volume, thickness, surface area, and subcortical volumes. Our findings reveal distinct spatial patterns of asymmetry, with early leftward asymmetry observed in association cortices and late rightward asymmetry in sensory regions. These trajectories support theories of the neuroplasticity of asymmetry and the role of both genetic and environmental factors in shaping brain lateralization. Additionally, we provide tools to generate asymmetry centile scores, which allow the quantification of individual deviations from typical asymmetry throughout the lifespan and can be applied to unseen data or clinical populations. We demonstrate the utility of these models by highlighting group-level differences in asymmetry in autism spectrum disorder, schizophrenia, and Alzheimers disease, and exploring genetic correlations with hemispheric specialization. To facilitate further research, we have made this normative framework freely available as an interactive open-access resource (upon publication), offering an essential tool to advance both basic and clinical neuroscience.
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