The Developing Human Connectome Project: A Fast Deep Learning-based Pipeline for Neonatal Cortical Surface Reconstruction

The Developing Human Connectome Project (dHCP) aims to explore developmental patterns of the human brain during the perinatal period. An automated processing pipeline has been developed to extract high-quality cortical surfaces from structural brain magnetic resonance (MR) images for the dHCP neonatal dataset. However, the current implementation of the pipeline requires more than 6.5 hours to process a single MRI scan, making it expensive for large-scale neuroimaging studies. In this paper, we propose a fast deep learning (DL) based pipeline for dHCP neonatal cortical surface reconstruction, incorporating DL-based brain extraction, cortical surface reconstruction and spherical projection, as well as GPU-accelerated cortical surface inflation and cortical feature estimation. We introduce a multiscale deformation network to learn diffeomorphic cortical surface reconstruction end-to-end from T2-weighted brain MRI. A fast unsupervised spherical mapping approach is integrated to minimize metric distortions between cortical surfaces and projected spheres. The entire workflow of our DL-based dHCP pipeline completes within only 24 seconds on a modern GPU, which is nearly 1000 times faster than the original dHCP pipeline. Manual quality control demonstrates that for 82.5% of the test samples, our DL-based pipeline produces superior (54.2%) or equal quality (28.3%) cortical surfaces compared to the original dHCP pipeline.

Studying the brain from adolescence to adulthood through sparse multi-view matrix factorisations

Men and women differ in specific cognitive abilities and in the expression of several neuropsychiatric conditions. Such findings could be attributed to sex hormones, brain differences, as well as a number of environmental variables. Existing research on identifying sex-related differences in brain structure have predominantly used cross-sectional studies to investigate, for instance, differences in average gray matter volumes (GMVs). In this article we explore the potential of a recently proposed multi-view matrix factorisation (MVMF) methodology to study structural brain changes in men and women that occur from adolescence to adulthood. MVMF is a multivariate variance decomposition technique that extends principal component analysis to "multi-view" datasets, i.e. where multiple and related groups of observations are available. In this application, each view represents a different age group. MVMF identifies latent factors explaining shared and age-specific contributions to the observed overall variability in GMVs over time. These latent factors can be used to produce low-dimensional visualisations of the data that emphasise age-specific effects once the shared effects have been accounted for. The analysis of two datasets consisting of individuals born prematurely as well as healthy controls provides evidence to suggest that the separation between males and females becomes increasingly larger as the brain transitions from adolescence to adulthood. We report on specific brain regions associated to these variance effects.