Alzheimer’s disease (AD) is an irreversible neurodegenerative disorder whose progression is closely associated with time. However, most diagnostic models are based on single time-point data, overlooking longitudinal disease characteristics. Structural magnetic resonance imaging (sMRI) has been widely utilized in the study of AD. To address the need for multi-time series analysis in longitudinal AD research and the integration of features from different brain tissues, we propose a Multi-Branch Fusion Channel Attention Network (MBFCA-Net) for disease diagnosis. This network leverages the temporal correlations across longitudinal scans for effective AD detection. We further conduct retrospective interpretability analysis to quantify the contributions of brain regions across disease stages. This enables a detailed investigation of dynamic changes in brain regions associated with AD and normal aging. The results indicate that the importance of regions such as the amygdala, parahippocampal gyrus, and temporal lobe undergoes dynamic changes throughout the progression of AD. Furthermore, AD-related voxel clusters exhibit a developmental trend, shifting from the hippocampus to the temporal lobe and transitioning from a dispersed to a more aggregated distribution. Our study provides novel insights into the longitudinal patterns of AD-related changes, offering valuable contributions to early diagnosis and pathological understanding of the disease.
Sun et al. (Thu,) studied this question.