ArticleFrontiers in neurology2013
Transfer Function between EEG and BOLD Signals of Epileptic Activity.
Article in Frontiers in neurology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Modeling the Hemodynamic Response Function Using EEG-fMRI Data During Eyes-Open Resting-State Conditions and Motor Task Execution.Brain topography · 2022Article
- Neurosurgery and artificial intelligence.AIMS neuroscience · 2021Review
- Localizing Epileptic Foci Using Simultaneous EEG-fMRI Recording: Template Component Cross-Correlation.Frontiers in neurology · 2021Article
- Identification of epileptic brain states by dynamic functional connectivity analysis of simultaneous EEG-fMRI: a dictionary learning approach.Scientific reports · 2019Article
- Semi-automated EEG Enhancement Improves Localization of Ictal Onset Zone With EEG-Correlated fMRI.Frontiers in neurology · 2019Article
- A Sparse EEG-Informed fMRI Model for Hybrid EEG-fMRI Neurofeedback Prediction.Frontiers in neuroscience · 2019Article
- EEG-Informed fMRI: A Review of Data Analysis Methods.Frontiers in human neuroscience · 2018Review
- Electrophysiological correlates of the BOLD signal for EEG-informed fMRI.Human brain mapping · 2015Review
- ICA extracts epileptic sources from fMRI in EEG-negative patients: a retrospective validation study.PloS one · 2013Article
- Identifying the epileptic network.Frontiers in neurology · 2013Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Simultaneous electroencephalogram (EEG)-functional Magnetic Resonance Imaging (fMRI) recordings have seen growing application in the evaluation of epilepsy, namely in the characterization of brain networks related to epileptic activity. In EEG-correlated fMRI studies, epileptic events are usually described as boxcar signals based on the timing information retrieved from the EEG, and subsequently convolved with a hemodynamic response function to model the associated Blood Oxygen Level Dependent (BOLD) changes. Although more flexible approaches may allow a higher degree of complexity for the hemodynamics, the issue of how to model these dynamics based on the EEG remains an open question. In this work, a new methodology for the integration of simultaneous EEG-fMRI data in epilepsy is proposed, which incorporates a transfer function from the EEG to the BOLD signal. Independent component analysis of the EEG is performed, and a number of metrics expressing different models of the EEG-BOLD transfer function are extracted from the resulting time courses. These metrics are then used to predict the fMRI data and to identify brain areas associated with the EEG epileptic activity. The methodology was tested on both ictal and interictal EEG-fMRI recordings from one patient with a hypothalamic hamartoma. When compared to the conventional analysis approach, plausible, consistent, and more significant activations were obtained. Importantly, frequency-weighted EEG metrics yielded superior results than those weighted solely on the EEG power, which comes in agreement with previous literature. Reproducibility, specificity, and sensitivity should be addressed in an extended group of patients in order to further validate the proposed methodology and generalize the presented proof of concept.
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