4D (spatial + temporal) infant cortical surface atlases covering dense time points are highly needed for understanding dynamic early brain development. In this article, we construct a set of 4D infant cortical surface atlases with longitudinally consistent and sharp cortical attribute patterns at 11 time points in the first six postnatal years, that is, at 1, 3, 6, 9, 12, 18, 24, 36, 48, 60, and 72 months of age, which is targeted for better normalization of the dynamic changing early brain cortical surfaces. To ensure longitudinal consistency and unbiasedness, we adopt a two‐stage group‐wise surface registration. To preserve sharp cortical attribute patterns on the atlas, instead of simply averaging over the coregistered cortical surfaces, we leverage a spherical patch‐based sparse representation using the augmented dictionary to overcome the potential registration errors. Our atlases provide not only geometric attributes of the cortical folding, but also cortical thickness and myelin content. Therefore, to address the consistency across different cortical attributes on the atlas, instead of sparsely representing each attribute independently, we jointly represent all cortical attributes with a group‐wise sparsity constraint. In addition, to further facilitate region‐based analysis using our atlases, we have also provided two widely used parcellations, that is, FreeSurfer parcellation and multimodal parcellation, on our 4D infant cortical surface atlases. Compared to cortical surface atlases constructed with other methods, our cortical surface atlases preserve sharper cortical folding attribute patterns, thus leading to better accuracy in registration of individual infant cortical surfaces to the atlas.

Deformable registration is fundamental to longitudinal and population-based image analyses. However, it is challenging to precisely align longitudinal infant brain MR images of the same subject, as well as cross-sectional infant brain MR images of different subjects, due to fast brain development during infancy. In this paper, we propose a recurrently usable deep neural network for the registration of infant brain MR images. There are three main highlights of our proposed method. (i) We use brain tissue segmentation maps for registration, instead of intensity images, to tackle the issue of rapid contrast changes of brain tissues during the first year of life. (ii) A single registration network is trained in a one-shot manner, and then recurrently applied in inference for multiple times, such that the complex deformation field can be recovered incrementally. (iii) We also propose both the adaptive smoothing layer and the tissue-aware anti-folding constraint into the registration network to ensure the physiological plausibility of estimated deformations without degrading the registration accuracy. Experimental results, in comparison to the state-of-the-art registration methods, indicate that our proposed method achieves the highest registration accuracy while still preserving the smoothness of the deformation field. The implementation of our proposed registration network is available online https://github.com/Barnonewdm/ACTA-Reg-Net .

Studying the early dynamic development of cortical folding with remarkable individual variability is critical for understanding normal early brain development and related neurodevelopmental disorders. This study focuses on the fingerprinting capability and the individual variability of cortical folding during early brain development. Specifically, we aim to explore (a) whether the developing neonatal cortical folding is unique enough to be considered as a “fingerprint” that can reliably identify an individual within a cohort of infants; (b) which cortical regions manifest more individual variability and thus contribute more for infant identification; (c) whether the infant twins can be distinguished by cortical folding. Hence, for the first time, we conduct infant individual identification and individual variability analysis involving twins based on the developing cortical folding features (mean curvature, average convexity, and sulcal depth) in 472 neonates with 1,141 longitudinal MRI scans. Experimental results show that the infant individual identification achieves 100% accuracy when using the neonatal cortical folding features to predict the identities of 1‐ and 2‐year‐olds. Besides, we observe high identification capability in the high‐order association cortices (i.e., prefrontal, lateral temporal, and inferior parietal regions) and two unimodal cortices (i.e., precentral gyrus and lateral occipital cortex), which largely overlap with the regions encoding remarkable individual variability in cortical folding during the first 2 years. For twins study, we show that even for monozygotic twins with identical genes and similar developmental environments, their cortical folding features are unique enough for accurate individual identification; and in some high‐order association cortices, the differences between monozygotic twin pairs are significantly lower than those between dizygotic twins. This study thus provides important insights into individual identification and individual variability based on cortical folding during infancy.

Alzheimer’s disease (AD) is a neurodegenerative disease with main symptoms of chronic primary memory loss and cognitive impairment. The study aim was to investigate the correlation between intrahippocampal functional connectivity (FC) and MRI radiomic features in AD. A total of 67 AD patients and 44 normal controls (NCs) were enrolled in this study. Using the seed-based method of resting-state functional MRI (rs-fMRI), the whole-brain FC with bilateral hippocampus as seed was performed, and the FC values were extracted from the bilateral hippocampus. We observed that AD patients demonstrated disruptive FC in some brain regions in the left hippocampal functional network, including right gyrus rectus, right anterior cingulate and paracingulate gyri, bilateral precuneus, bilateral angular gyrus, and bilateral middle occipital gyrus. In addition, decreased FC was detected in some brain regions in the right hippocampal functional network, including bilateral anterior cingulate and paracingulate gyri, right dorsolateral superior frontal gyrus, and right precentral gyrus. Bilateral hippocampal radiomics features were calculated and selected using the A.K. software. Finally, Pearson’s correlation analyses were conducted between these selected features and the bilateral hippocampal FC values. The results suggested that two gray level run-length matrix (RLM) radiomic features and one gray level co-occurrence matrix (GLCM) radiomic feature weakly associated with FC values in the left hippocampus. However, there were no significant correlations between radiomic features and FC values in the right hippocampus. These findings present that the AD group showed abnormalities in the bilateral hippocampal functional network. This is a prospective study that revealed the weak correlation between the MRI radiomic features and the intrahippocampal FC in AD patients.

The early postnatal period witnesses rapid and dynamic brain development. However, the relationship between brain anatomical structure and cognitive ability is still unknown. Currently, there is no explicit model to characterize this relationship in the literature. In this paper, we explore this relationship by investigating the mapping between morphological features of the cerebral cortex and cognitive scores. To this end, we introduce a multi-view multi-task learning approach to intuitively explore complementary information from different time-points and handle the missing data issue in longitudinal studies simultaneously. Accordingly, we establish a novel model, latent partial multi-view representation learning. Our approach regards data from different time-points as different views and constructs a latent representation to capture the complementary information from incomplete time-points. The latent representation explores the complementarity across different time-points and improves the accuracy of prediction. The minimization problem is solved by the alternating direction method of multipliers. Experimental results on both synthetic and real data validate the effectiveness of our proposed algorithm.

Prediction of the chronological age based on neuroimaging data is important for brain development analysis and brain disease diagnosis. Although many researches have been conducted for age prediction of older children and adults, little work has been dedicated to infants. To this end, this paper focuses on predicting infant age from birth to 2-year old using brain MR images, as well as identifying some related biomarkers. However, brain development during infancy is too rapid and heterogeneous to be accurately modeled by the conventional regression models. To address this issue, a two-stage prediction method is proposed. Specifically, our method first roughly predicts the age range of an infant and then finely predicts the accurate chronological age based on a learned, age-group-specific regression model. Combining this two-stage prediction method with another complementary one-stage prediction method, a hierarchical rough-to-fine (HRtoF) model is built. HRtoF effectively splits the rapid and heterogeneous changes during a long time period into several short time ranges and further mines the discrimination capability of cortical features, thus reaching high accuracy in infant age prediction. Taking 8 types of cortical morphometric features from structural MRI as predictors, the effectiveness of our proposed HRtoF model is validated using an infant dataset including 50 healthy subjects with 251 longitudinal MRI scans from 14 to 797 days. Comparing with five state-of-the-art regression methods, HRtoF model reduces the mean absolute error of the prediction from >48 days to 32.1 days. The correlation coefficient of the predicted age and the chronological age reaches 0.963. Moreover, based on HRtoF, the relative contributions of the eight types of cortical features for age prediction are also studied.