Abnormal Cortical Thickness and Structural Covariance Networks in Systemic Lupus Erythematosus Patients without Major Neuropsychiatric Manifestations

Abstract

Background Non-neuropsychiatric systemic lupus erythematosus (non-NPSLE) has been confirmed to have subtle changes in brain structure before the appearance of obvious neuropsychiatric symptoms. Previous literature mainly focuses on brain structure loss in non-NPSLE; however, the results are heterogeneous, and the impact of structural changes on the topological structure of patients' brain network remains to be determined. In this study, we combined neuroimaging and network analysis methods to evaluate the changes in cortical thickness and its structural covariance networks (SCNs) in patients with non-NPSLE. Methods We compare the cortical thickness of non-NPSLE patients (N = 108) and healthy controls (HCs, N = 88) using both surface-based morphometry (SBM) and regions of interest (ROIs) method, respectively. After that, we analyzed the correlation between the abnormal cortical thickness results found in the ROIs method and a series of clinical features. Finally, we constructed the SCNs of two groups using the regional cortical thickness, and analyzed the abnormal SCNs of non-NPSLE. Results By SBM method, we found that cortical thickness of 34 clusters in the non-NPSLE group was thinner than that in the HCs group. ROIs method based on Destrieux altas showed that cortical thickness of 57 regions in the non-NPSLE group was thinner than that in the HCs group and related to the course of disease, autoantibodies, the cumulative amount of immunosuppressive agents, and cognitive psychological scale. In the SCNs analysis, the cortical thickness SCNs of the non-NPSLE group did not follow the small-world attribute at a few densities, and the global clustering coefficient appeared to increase. The area under the curve analysis showed that there were significant differences between the two groups in clustering coefficient, degree, betweenness, and local efficiency. There are a total of seven hubs for non-NPSLE, and five hubs in HCs, the two groups do not share a common hub distribution. Conclusion Extensive and obvious reduction in cortical thickness and abnormal topological organization of SCNs are observed in non-NPSLE patients. The observed abnormalities may not only be the realization of brain damage caused by the disease, but also the contribution of the compensatory changes within the nervous system.