Various disease conditions can alter EEG event-related responses and fMRI-BOLD signals. We hypothesized that event-related responses and their clinical alterations are imprinted in the EEG spectral domain as event-related (spatio)spectral patterns (ERSPat). We tested four EEG-fMRI fusion models utilizing EEG power spectra fluctuations (i.e., absolute spectral model - ASM; relative spectral model - RSM; absolute spatiospectral model - ASSM; and relative spatiospectral model - RSSM) for fully automated and blind visualization of task-related neural networks. Two (spatio)spectral patterns (high band and low band) demonstrated significant negative linear relationship ( < 0.05) to the frequent stimulus and three patterns (two low and bands, and narrow band) demonstrated significant positive relationship ( < 0.05) to the target stimulus. These patterns were identified as ERSPats. EEG-fMRI F-map of each model showed strong engagement of insula, cuneus, precuneus, basal ganglia, sensory-motor, motor and dorsal part of fronto-parietal control (FPCN) networks with fast HRF peak and noticeable trough. ASM and RSSM emphasized spatial statistics, and the relative power amplified the relationship to the frequent stimulus. For the model, we detected a reduced HRF peak amplitude and a magnified HRF trough amplitude in the frontal part of the FPCN, default mode network (DMN) and in the frontal white matter. The frequent-related patterns visualized less significant and distinct suprathreshold spatial associations. Each model showed strong involvement of lateralized left-sided sensory-motor and motor networks with simultaneous basal ganglia co-activations and reduced HRF peak and amplified HRF trough in the frontal part of the FPCN and DMN. The ASM model preserved target-related EEG-fMRI associations in the dorsal part of the FPCN. For , , and bands, all models provided high local F-statistics in expected regions. The most robust EEG-fMRI associations were observed for ASM and RSSM.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107237PMC
http://dx.doi.org/10.3389/fneur.2021.644874DOI Listing

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