Altered structural covariance of hippocampal subregions in patients with Alzheimer's disease

Background and purpose: Different atrophy of hippocampus subregions is a valuable indicator of patients with Alzheimer's disease (AD). To explore the relationship among the hippocampal subregions of patients with AD, altered gray matter structural covariance of hippocampal subregions in patients with AD was studied.

Materials and methods: Participants were selected from the Open Access Series of Imaging Studies Database. Pearson correlations among the volume of the hippocampal subregions were generated as structural covariance network. Topological metrics for all selected sparsity ranges were calculated in the healthy controls (HCs) and patients with AD by using the GRETNA software package. Spearman correlation analysis was performed to statistically analyze the volume and Mini-mental State Examination (MMSE) scores of the hippocampal subregions of the patients with AD, with age and gender as interference covariates and corrected for false discovery rate (FDR) (p < 0.05).

Results: The structural covariance network properties of the hippocampal subregions of patients with AD changed. The clustering coefficient (Cp) and network efficiency (Ne) decreased, characteristic path length (Lp) increased, and the hub nodes changed. The volumes of left parasubiculum, right granule cell layer of dentate gyrus (GC-DG), right molecular layer of the hippocampus (molecular_layer_HP), right Cornu Ammonis (CA) regions CA1 of the hippocampus proper, right fimbria and right CA4 were significantly correlated with the MMSE scores.

Conclusions: The structural covariance network of the hippocampal subregions of patients with AD was reorganized, and the transmission efficiency was weakened. This study explored the changes in these subregions from the network level, which may provide a new perspective and theoretical basis for the neurobiological mechanisms of patients with AD.