4.7 Article

Continuous EEG source imaging enhances analysis of EEG-fMRI in focal epilepsy

Journal

NEUROIMAGE
Volume 49, Issue 4, Pages 3219-3229

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2009.11.055

Keywords

EEG; Source imaging; Epilepsy; Interictal; fMRI

Funding

  1. Center for Biomedical Imaging (CIBM) of Geneva
  2. Fonds de Perfectionnement of the University Hospital of Geneva
  3. Swiss National Science Foundation [32-111783, 33CM30-124115, 33CM30-124089]
  4. UK Medical Research Council [G0301067]
  5. Big Lottery Fund
  6. Wolfson Trust
  7. National Society for Epilepsy
  8. Department of Health's NIHR Biomedical Research Centres funding scheme
  9. MRC [G9805989, G0301067] Funding Source: UKRI
  10. Medical Research Council [G0301067, G9805989, G0200216] Funding Source: researchfish
  11. National Institute for Health Research [NF-SI-0509-10161] Funding Source: researchfish

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Introduction: EEG-correlated fMRI (EEG-fMRI) Studies can reveal haemodynamic changes associated with Interictal Epileptic Discharges (IED). Methodological improvements are needed to increase sensitivity and specificity for localising the epileptogenic zone. We investigated whether the estimated EEG source activity improved models of the BOLD changes in EEG-fMRI data, compared to conventional a event-related D designs based solely on the visual identification of IED. Methods: Ten patients with pharmaco-resistant focal epilepsy underwent EEG-fMRI. EEG Source Imaging (ESI) was performed on intra-fMRI averaged IED to identify the irritative zone. The continuous activity of this estimated IED source (cESI) over the entire recording was used for fMRI analysis (cESI model). The maps of BOLD signal changes explained by cESI were compared to results of the conventional IED-related model. Results: ESI was concordant with non-invasive data in 13/15 different types of IED. The cESI model explained significant additional BOLD variance in regions concordant with video-EEG, structural MRI or, when available, intracranial EEG in 10/15 IED. The cESI model allowed better detection of the BOLD cluster, concordant with intracranial EEG in 4/7 IED, compared to the IED model. In 4 IED types, cESI-related BOLD signal changes were diffuse with a pattern suggestive of contamination of the source signal by artefacts, notably incompletely corrected motion and pulse artefact. In one IED type, there was no significant BOLD change with either model. Conclusion: Continuous EEG source imaging can improve the modelling of BOLD changes related to interictal epileptic activity and this may enhance the localisation of the irritative zone. (C) 2009 Elsevier Inc. All tights reserved.

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