ArticleFrontiers in neuroscience2025
Spatio-temporal dynamic functional brain network for mild cognitive impairment analysis.
Article in Frontiers in neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- APOE ε4-related structural vulnerability in mild cognitive impairment: a subsystem-based analysis of the default mode network.Research square · 2026Article
- A game-theoretic framework for multimodal information utilization under heterogeneous processing environments in neuroscience and perception science.Frontiers in neuroscience · 2026Article
- Precision neurodiversity: personalized brain network architecture as a window into cognitive variability.Frontiers in human neuroscience · 2025Review
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5 authors.
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Abstract
Introduction: Alzheimer's Disease (AD) is a progressive neurodegenerative disorder, with Mild Cognitive Impairment (MCI) often serving as a prodromal stage. Early detection of MCI is critical for timely intervention. Methods: Dynamic Functional Connectivity analysis reveals temporal dynamics obscured by static functional connectivity, making it valuable for analyzing and classifying psychiatric disorders. This study proposes a novel spatio-temporal approach for analyzing dynamic brain networks using resting-state fMRI. The method was evaluated on data from 85 subjects (33 healthy controls, 29 Early Mild Cognitive Impairment (EMCI), 23 AD) from the ADNI dataset. Results: Our model outperformed existing techniques, achieving 83.9% accuracy and 83.1% AUC in distinguishing AD from healthy controls. Discussion: In addition to improved classification performance, key affected regions such as left hippocampus, the right amygdala, the left inferior parietal lobe, the left olfactory cortex, the right precuneus, and the insula, were identified-areas known to be associated with memory function and early Alzheimer's pathology. These findings suggest that dynamic connectivity analysis holds promise for non-invasive and interpretable early-stage diagnosis of AD.
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