ArticleHealth information science and systems2025
Reconstructing brain causal dynamics for subject and task fingerprints using fMRI time-series data.
Article in Health information science and systems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Purpose: Recently, there has been a revived interest in system neuroscience causation models, driven by their unique capability to unravel complex relationships in multi-scale brain networks. In this paper, we present a novel method that leverages causal dynamics to achieve effective fMRI-based subject and task fingerprinting. Methods: By applying an implicit-explicit discretization scheme, we develop a two-timescale linear state-space model. Through data-driven identification of its parameters, the model captures causal signatures, including directed interactions among brain regions from a spatial perspective, and disentangled fast and slow dynamic modes of brain activity from a temporal perspective. These causal signatures are then integrated with: (i) a modal decomposition and projection method for model-based subject identification, and (ii) a Graph Neural Network (GNN) framework for learning-based task classification. Furthermore, we introduce the concept of the brain reachability landscape as a novel visualization tool, which quantitatively characterizes the maximum possible activation levels of brain regions under various fMRI tasks. Results: We evaluate the proposed approach using the Human Connectome Project dataset and demonstrate its advantage over non-causality-based methods. The obtained causal signatures are visualized and demonstrate clear biological relevance with established understandings of brain function. Conclusion: We verified the feasibility and effectiveness of utilizing brain causal signatures for subject and task fingerprinting. Additionally, our work paves the way for further studies on causal fingerprints with potential applications in both healthy controls and neurodegenerative diseases.
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