Abstract Fine-scale spatial dynamics within functional brain networks manifest as high spatial-frequency variations that conventional independent component analysis (ICA) methods fail to capture. These subtle changes may carry critical information about transient connectivity and disordered brain function. We developed NeuroMark-DyFICA (dynamic frequency-informed ICA), a novel framework to enhance detection of spatiotemporal variability in fMRI data. It integrates three stages: dynamic NeuroMark ICA across sliding windows to estimate time-varying, spatially constrained networks; high-pass spatial filtering to emphasize fine-scale spatial features; and group-level ICA to extract refined dynamic components with subject-specific mixing weights. Unlike prior NeuroMark applications or conventional dynamic ICA, NeuroMark-DyFICA establishes a reproducible latent space of high-frequency dynamics, uniquely capturing transient, fine-scale reconfigurations of network topography. Validation using a controlled 2D simulation demonstrated reliable detection of subtle spatial shifts mimicking pathology, which conventional ICA failed to recover. Applying to resting-state fMRI from schizophrenia patients and healthy controls, multiple networks were estimated. We highlight six representative systems (thalamus, auditory, visual/fusiform, middle frontal, default mode, cerebellum). Results revealed two complementary abnormalities in schizophrenia: an imbalance between inactive and hyper-engaged states and altered convergence among dynamic states. NeuroMark-DyFICA reveals fine-grained spatiotemporal disruptions in brain networks, offering mechanistic insights and potential biomarkers for psychiatric disorders.
Behzadfar et al. (Fri,) studied this question.