Abstract

Longitudinal studies measuring changes in cortical morphology over time are best facilitated by parcellation schemes compatible across all life stages. The Melbourne Children’s Regional Infant Brain (M-CRIB) and M-CRIB 2.0 atlases provide voxel-based parcellations of the cerebral cortex compatible with the Desikan-Killiany (DK) and the Desikan-Killiany-Tourville (DKT) cortical labelling schemes. This study introduces surface-based versions of the M-CRIB and M-CRIB 2.0 atlases, termed M-CRIB-S(DK) and M-CRIB-S(DKT), with a pipeline for automated parcellation utilizing FreeSurfer and developing Human Connectome Project (dHCP) tools. Using T2-weighted magnetic resonance images of healthy neonates (n = 58), we created average spherical templates of cortical curvature and sulcal depth. Manually labelled regions in a subset (n = 10) were encoded into the spherical template space to construct M-CRIB-S(DK) and M-CRIB-S(DKT) atlases. Labelling accuracy was assessed using Dice overlap and boundary discrepancy measures with leave-one-out cross-validation. Cross-validated labelling accuracy was high for both atlases (average regional Dice = 0.79–0.83). Worst-case boundary discrepancy instances ranged from 9.96–10.22 mm, which appeared to be driven by variability in anatomy for some cases. The M-CRIB-S atlas data and automatic pipeline allow extraction of neonatal cortical surfaces labelled according to the DK or DKT parcellation schemes.

Highlights

  • Longitudinal studies measuring changes in cortical morphology over time are best facilitated by parcellation schemes compatible across all life stages

  • Tools tuned for adult brains, such as the adult T1-based templates and atlases provided in FreeSurfer[5,8], are not directly applicable to neonatal brain images

  • In this study we aimed to provide neonatal average surface templates and surface-based cortical atlases based on the Melbourne Children’s Regional Infant Brain (M-CRIB) and M-CRIB 2.0 parcellation schemes, that are compatible with FreeSurfer and the developing Human Connectome Project (dHCP) pipelines[2,5,8]

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Summary

Introduction

Longitudinal studies measuring changes in cortical morphology over time are best facilitated by parcellation schemes compatible across all life stages. The Melbourne Children’s Regional Infant Brain (M-CRIB) and M-CRIB 2.0 atlases provide voxel-based parcellations of the cerebral cortex compatible with the Desikan-Killiany (DK) and the Desikan-Killiany-Tourville (DKT) cortical labelling schemes. The M-CRIB-S atlas data and automatic pipeline allow extraction of neonatal cortical surfaces labelled according to the DK or DKT parcellation schemes. Labelling a neonatal brain image using adult-derived atlases is problematic, due to the inherent difference in anatomy and tissue composition between infant and adult brains[15]. While accurate labelling can be achieved using voxel-based parcellation schemes[16,18,20], surface-based registration methods lead to significantly improved alignment of cortical landmarks, including cortical folds, and more accurate placement of areal boundaries[21,22]

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