Irina Grigorescu

Yilan Dong, Vanessa Kyriakopoulou, Irina Grigorescu et al.

Numerous studies have highlighted that atypical brain development, particularly during infancy and toddlerhood, is linked to an increased likelihood of being diagnosed with a neurodevelopmental condition, such as autism. Accurate brain tissue segmentations for morphological analysis are essential in numerous infant studies. However, due to ongoing white matter (WM) myelination changing tissue contrast in T1- and T2-weighted images, automatic tissue segmentation in 6-month infants is particularly difficult. On the other hand, manual labelling by experts is time-consuming and labor-intensive. In this study, we propose the first 8-tissue segmentation pipeline for six-month-old infant brains. This pipeline utilizes domain adaptation (DA) techniques to leverage our longitudinal data, including neonatal images segmented with the neonatal Developing Human Connectome Project structural pipeline. Our pipeline takes raw 6-month images as inputs and generates the 8-tissue segmentation as outputs, forming an end-to-end segmentation pipeline. The segmented tissues include WM, gray matter (GM), cerebrospinal fluid (CSF), ventricles, cerebellum, basal ganglia, brainstem, and hippocampus/amygdala. Cycle-Consistent Generative Adversarial Network (CycleGAN) and Attention U-Net were employed to achieve the image contrast transformation between neonatal and 6-month images and perform tissue segmentation on the synthesized 6-month images (neonatal images with 6-month intensity contrast), respectively. Moreover, we incorporated the segmentation outputs from Infant Brain Extraction and Analysis Toolbox (iBEAT) and another Attention U-Net to further enhance the performance and construct the end-to-end segmentation pipeline. Our evaluation with real 6-month images achieved a DICE score of 0.92, an HD95 of 1.6, and an ASSD of 0.42.

Paula Ramirez, Alena Uus, Milou P. M. van Poppel et al.

Congenital Heart Disease (CHD) is a group of cardiac malformations present already during fetal life, representing the prevailing category of birth defects globally. Our aim in this study is to aid 3D fetal vessel topology visualisation in aortic arch anomalies, a group which encompasses a range of conditions with significant anatomical heterogeneity. We present a multi-task framework for automated multi-class fetal vessel segmentation from 3D black blood T2w MRI and anomaly classification. Our training data consists of binary manual segmentation masks of the cardiac vessels' region in individual subjects and fully-labelled anomaly-specific population atlases. Our framework combines deep learning label propagation using VoxelMorph with 3D Attention U-Net segmentation and DenseNet121 anomaly classification. We target 11 cardiac vessels and three distinct aortic arch anomalies, including double aortic arch, right aortic arch, and suspected coarctation of the aorta. We incorporate an anomaly classifier into our segmentation pipeline, delivering a multi-task framework with the primary motivation of correcting topological inaccuracies of the segmentation. The hypothesis is that the multi-task approach will encourage the segmenter network to learn anomaly-specific features. As a secondary motivation, an automated diagnosis tool may have the potential to enhance diagnostic confidence in a decision support setting. Our results showcase that our proposed training strategy significantly outperforms label propagation and a network trained exclusively on propagated labels. Our classifier outperforms a classifier trained exclusively on T2w volume images, with an average balanced accuracy of 0.99 (0.01) after joint training. Adding a classifier improves the anatomical and topological accuracy of all correctly classified double aortic arch subjects.

Nashira Baena, Mariana da Silva, Irina Grigorescu et al.

Understanding individual cortical development is essential for identifying deviations linked to neurodevelopmental disorders. However, current normative modelling frameworks struggle to capture fine-scale anatomical details due to their reliance on modelling data within a population-average reference space. Here, we present a novel framework for learning individual growth trajectories from biomechanically constrained, longitudinal, diffeomorphic image registration, implemented via a hierarchical network architecture. Trained on neonatal MRI data from the Developing Human Connectome Project, the method improves the biological plausibility of warps, generating growth trajectories that better follow population-level trends while generating smoother warps, with fewer negative Jacobians, relative to state-of-the-art baselines. The resulting subject-specific deformations provide interpretable, biologically grounded mappings of development. This framework opens new possibilities for predictive modeling of brain maturation and early identification of malformations of cortical development.