Causal Structural Covariance Network Suggesting Structural Alterations Progression in Type 2 Diabetes Patients.

Background and Purpose: According to reports, type 2 diabetes (T2D) is a progressive disease. However, no known research has examined the progressive brain structural changes associated with T2D. The purpose of this study was to determine whether T2D patients exhibit progressive brain structural alterations and, if so, how the alterations progress. Materials and Methods: Structural magnetic resonance imaging scans were collected for 81 T2D patients and 48 sex-and age-matched healthy controls (HCs). Voxel-based morphometry (VBM) and causal structural covariance network (CaSCN) analyses were applied to investigate gray matter volume (GMV) alterations and the likely chronological processes underlying them in T2D. Two sample t-tests were performed to compare group differences, and the differences were corrected using Gaussian random field (GRF) correction (voxel-level p < 0.001, cluster-level p < 0.01). Results: Our findings demonstrated that GMV alterations progressed in T2D patients as disease duration increased. In the early stages of the disease, the right temporal pole of T2D patients had GMV atrophy. As the diseases duration prolonged, the limbic system, cerebellum, subcortical structures, parietal cortex, frontal cortex, and occipital cortex progressively exhibited GMV alterations. The patients also exhibited a GMV alterations sequence exerting from the right temporal pole to the limbic-cerebellum-striatal-cortical network areas. Conclusion: Our results indicate that the progressive GMV alterations of T2D patients manifested a limbic-cerebellum-striatal-cortical sequence. These findings may contribute to a better understanding of the progression and an improvement of current diagnosis and intervention strategies for T2D.

Group-guided individual functional parcellation of the hippocampus and application to normal aging.

Aging is closely associated with cognitive decline affecting attention, memory and executive functions. The hippocampus is the core brain area for human memory, learning, and cognition processing. To delineate the individual functional patterns of hippocampus is pivotal to reveal the neural basis of aging. In this study, we developed a group-guided individual parcellation approach based on semisupervised affinity propagation clustering using the resting-state functional magnetic resonance imaging to identify individual functional subregions of hippocampus and to identify the functional patterns of each subregion during aging. A three-way group parcellation was yielded and was taken as prior information to guide individual parcellation of hippocampus into head, body, and tail in each subject. The superiority of individual parcellation of hippocampus is validated by higher intraregional functional similarities by compared to group-level parcellation results. The individual variations of hippocampus were associated with coactivation patterns of three typical functions of hippocampus. Moreover, the individual functional connectivities of hippocampus subregions with predefined target regions could better predict age than group-level functional connectivities. Our study provides a novel framework for individual brain functional parcellations, which may facilitate the future individual researches for brain cognitions and brain disorders and directing accurate neuromodulation.

Dynamic changes of large-scale resting-state functional networks in major depressive disorder.

Sliding window method is widely used to study the functional connectivity dynamics in brain networks. A key issue of this method is how to choose the window length and number of clusters across different window length. Here, we introduced a universal method to determine the optimal window length and number of clusters and applied it to study the dynamic functional network connectivity (FNC) in major depressive disorder (MDD). Specifically, we first extracted the resting-state networks (RSNs) in 27 medication-free MDD patients and 54 healthy controls using group independent component analysis (ICA), and constructed the dynamic FNC patterns for each subject in the window range of 10-80 repetition times (TRs) using sliding window method. Then, litekmeans algorithm was utilized to cluster the FNC patterns corresponding to each window length into 2-20 clusters. The optimal number of clusters was determined by voting method and the optimal window length was determined by identifying the most representative window length. Finally, 8 recurring FNC patterns regarded as FNC states were captured for further analyzing the dynamic attributes. Our results revealed that MDD patients showed increased mean dwell time and fraction of time spent in state #5, and the mean dwell time is correlated with depression symptom load. Additionally, compared with healthy controls, MDD patients had significantly reduced FNC within FPN in state #7. Our study reported a new approach to determine the optimal window length and number of clusters, which may facilitate the future study of the functional dynamics. These findings about MDD using dynamic FNC analyses provide new evidence to better understand the neuropathology of MDD.