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Updated: Feb 28, 2026

Application of Granger Causality Analysis of the Directed Functional Connection in Alzheimer's Disease and Mild Cognitive Impairment
Published on: August 7, 2017
Interpretable Network-Level Biomarker Discovery for Alzheimer's Stage Assessment Using Resting-State fNIRS Complexity
Min-Kyoung Kang1, Agatha Elisabet1, So-Hyeon Yoo2
1School of Mechanical Engineering, Pusan National University, Busan 46241, Republic of Korea.
None:
Background/Objectives: This study introduces a reproducible and interpretable graph-based framework for resting-state functional near-infrared spectroscopy (fNIRS) that enables network-level biomarker discovery for Alzheimer's disease (AD). Although resting-state fNIRS is well suited for task-free assessment, most existing approaches rely on static channel-wise features or conventional functional connectivity, limiting insight into coordinated network dynamics and reproducibility. Methods: Resting-state prefrontal fNIRS signals were represented as subject-level graphs in which edges captured coordinated fluctuations of nonlinear signal complexity across channels, computed using sliding-window analysis. Graph neural networks (GNNs) were employed as analytical tools to identify disease-stage-related network patterns. Interpretability was assessed using edge-level importance measures, and reproducibility was evaluated through fold-wise stability analysis and consensus network construction. Results: The proposed complexity-fluctuation-based graph representation consistently outperformed conventional amplitude-based functional connectivity. Statistically supported prefrontal network biomarkers distinguishing mild cognitive impairment (MCI) from healthy aging were identified, with statistically significant group differences (p = 0.001). In contrast, network patterns associated with Alzheimer's disease were more heterogeneous and less consistently expressed. Consensus analysis revealed a subset of prefrontal connections repeatedly selected across cross-validation folds, and attention-based network patterns showed strong spatial correspondence with statistically derived biomarkers. Conclusions: This study establishes a reproducible and interpretable framework for resting-state fNIRS analysis that emphasizes coordinated complexity dynamics rather than classification accuracy. The results indicate that network-level alterations are most consistently expressed at the MCI stage, highlighting its role as a critical transitional state and supporting the potential of the proposed approach for longitudinal monitoring and clinically applicable fNIRS-based assessment of neurodegenerative disease.
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