| Literature DB >> 26872220 |
Maria Centeno1,2, Tim M Tierney1, Suejen Perani1,3, Elhum A Shamshiri1, Kelly StPier2, Charlotte Wilkinson2, Daniel Konn4, Tina Banks1, Serge Vulliemoz5, Louis Lemieux6, Ronit M Pressler2, Christopher A Clark1, J Helen Cross1,2, David W Carmichael1.
Abstract
BACKGROUND: Early surgical intervention in children with drug resistant epilepsy has benefits but requires using tolerable and minimally invasive tests. EEG-fMRI studies have demonstrated good sensitivity for the localization of epileptic focus but a poor yield although the reasons for this have not been systematically addressed. While adults EEG-fMRI studies are performed in the "resting state"; children are commonly sedated however, this has associated risks and potential confounds. In this study, we assessed the impact of the following factors on the tolerability and results of EEG-fMRI in children: viewing a movie inside the scanner; movement; occurrence of interictal epileptiform discharges (IED); scan duration and design efficiency. This work's motivation is to optimize EEG-fMRI parameters to make this test widely available to paediatric population.Entities:
Mesh:
Year: 2016 PMID: 26872220 PMCID: PMC4752259 DOI: 10.1371/journal.pone.0149048
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Clinical and EEG-fMRI information: Summary of each case’s clinical and radiological information.
The presumed epileptogenic region is established during the presurgical evaluation process for each patient after evaluation of a panel of tests. N IED types is the number of different IED identified in each subject and IED/ session shows the mean number of IED in each session. EEG interictal epileptiform discharges (IED) column shows the field of the epileptiform activity captured during EEG-fMRI scan. EEG-fMRI map shows the classification of the maps: concordant or discordant. Ep. Region: epileptogenic F: Female; M: male: L left; R: right; FCD: focal cortical dysplasia. N/A: non applicable. T-P-O: Temporo-parieto-occipital C: Concordant EEG-fMRI map with epileptogenic region, D: Discordant EEG-fMRI map with epileptogenic region.
| ID | Age/ Gender | Presumed ep. region | MRI lesion/location | NIED types | IED/session | EEG IED | BOLD in ep. region | BOLD outside ep. region | EEG-fMRI map classification |
|---|---|---|---|---|---|---|---|---|---|
| 8F | L Temporal | Tuberosclerosis. Left temporal prominent tuber | 1 | 5 | L temporal | N | N | D | |
| 14F | L Frontal pole | N/A | No IED | N/A | |||||
| 11M | Hypothalamus/L Temporal | Hypothalamic hamartoma | 1 | 34.5 | Left temporal | N | Y | D | |
| 15M | L posterior quadrant | N/A | No IED | N/A | |||||
| 11F | R Fronto-temporal | N/A | 1 | 40.5 | R Fronto-temporal | N | N | D | |
| 17M | R Parietal | R parietal FCD. Residual lesion after surgery | 4 | 167 | R Temporal | Y | N | C | |
| 15M | R Frontal-central | N/A | No IED | N/A | |||||
| 15M | L Temporal/R Frontal | L Temporal lobe FCD | 3 | 219 | R Frontal | Y | Y | C | |
| 11F | L Frontal-central | L hemisphere cortical atrophy perinatal | 1 | 237.6 | L central | Y | N | C | |
| 14F | R Temporal | R temporal FCD 2B | 2 | 169 | R Temporal | Y | Y | C | |
| 11F | R Fronto-temporal | N/A | 1 | 134.7 | R Fronto-temporal | Y | Y | C | |
| 11F | R Frontal pole | R frontal pole FCD | 1 | 129.5 | R Fronto-polar | Y | Y | C | |
| 12M | R central | Skull malformation/ R hemispheric cortical atrophy | 3 | 151 | R central | N | Y | D | |
| 17F | R Frontal | N/A | 1 | 50 | R Frontal | Y | Y | C | |
| 16F | L Frontal | N/A | 1 | 10.5 | Bifrontal spike-wave runs | Y | Y | C | |
| 11F | L Frontal | N/A | 1 | 20 | L Frontal lateral | N | Y | D | |
| 14M | L Fronto-temporal | L hemisphere cortical atrophy Autoinmune | 2 | 187.2 | L Temporal | Y | Y | C | |
| 16F | L posterior insula | L insular FCD | 1 | 66.7 | L central | N | N | D | |
| 18M | R parietal superior and medial | R precuneus FCD 2A | 1 | 44.7 | R Parietal | N | Y | D | |
| 11M | R Frontal | N/A | 2 | 151.2 | R Frontal | Y | Y | C | |
| 16F | L posterior quadrant/L frontal | L T-P-O polymicrogyria /Unspecific cortical atrophy | 3 | 261.5 | L posterior quadrant | Y | Y | C | |
| 15M | L Temporo-occipital | L HS | 2 | 101 | L posterior quadrant | Y | Y | C | |
| 17F | L Temporal | N/A | No IED | N/A | |||||
| 17F | L Frontal | N/A | No IED | N/A | |||||
| 8F | L Frontal | L middle cerebral artery stroke | 1 | 107 | Bifrontal spike-wave runs | Y | Y | C | |
| 16M | R Frontal | N/A | 2 | 114.2 | R Frontal | N | N | D | |
| 11M | L posterior quadrant | L choroid plexus papilloma L posterior quadrant atrophy secondary to radiotherapy | 2 | 294 | L posterior quadrant | N | N | D | |
| 13M | L Frontal | L middle frontal gyrus FCD | 1 | 29 | L Frontal | N | N | D | |
| 10F | L Frontal | N/A | 2 | 87.5 | L Frontal | N | N | D | |
| 11M | R posterior quadrant | N/A | 3 | 53.5 | R posterior quadrant | Y | Y | C | |
| 14M | L Occipital | L posterior artery stroke | 1 | 57.5 | L Occipital | Y | Y | C | |
| 17M | L Frontal | N/A | No IED | N/A | |||||
| 17M | R Occipital | L occipital atrophy. Iquemic perinatal insult | 1 | 40.25 | L Occipital | Y | Y | C | |
| 13M | L Occipital | L T-P-O cortical atrophy perinatal | 3 | 64 | L posterior quadrant | Y | Y | C | |
| 18F | R Frontal | Right frontal FCD | No IED | N/A | |||||
| 17F | R Frontal/R temporal | Bilateral oribito-frontal polymicrogyria | 2 | 219 | R Temporal | Y | Y | C | |
| 18F | R F-T-P junction | R T-P-O junction postusurgery residual FCD | No IED | N/A | |||||
| 11F | R Parietal | N/A | 1 | 77.5 | R central | N | N | D | |
| 18M | R Parietal | R inferior parietal residual postsurgical DNET | 2 | 94.5 | R Parietal | N | Y | D | |
| 11F | R Parietal | R parietal FCD | 1 | 375.75 | R Parietal | Y | Y | C | |
| 13F | R medial Temporal | R amygdala DNET | 1 | 126.75 | R anterior Temporal | Y | Y | C | |
| 12M | R Perisylvian | Bilateral perisylvian polymicrogyria | 1 | 13.75 | R posterior Fronto-Parietal | N | Y | D | |
| 17F | L Frontal | N/A | 2 | 78.7 | L Frontal-vertex | Y | Y | C | |
| 13F | L Frontal | L inferior frontal FCD | 2 | 135.5 | L Frontal lateral | Y | Y | C | |
| 15F | R posterior cingualte | R posterior cingulate DNET | 1 | 47 | R Frontal | N | Y | D | |
| 7M | L Frontal | N/A | 1 | 74.5 | L Frontal vertex | Y | Y | C |
Fig 1Clinical assessment of the EEG-fMRI maps.
EEG-fMRI maps are compared with the location of the presumed epileptogenic region (green area). Epileptogenic region is assessed clinically based on multimodal tests. Maps are classified as Concordant if a cluster of significant activation is present in the epileptogenic region and Discordant otherwise.
Fig 2Movement as a function of time.
There is an increase of movement of approximately 40% in the second and third session and of 100% in the fourth session relative to the first. The bars represent the mean in-scanner movement for each session across patients and controls irrespective of the effect of video and age. The standard error is represented by T bars. Amount of movement for sessions 2–3 and 4 were significantly greater compared to session 1 (p< 0.05). Significant differences marked with asterisk.
Fig 3Rate of interictal epileptiform discharges (IED).
Bar represent mean number of IED per minute during the resting state sessions and during the two conditions of the video session (video clip and “please wait” screen). There is no significant difference between the rates of IED in these three conditions.
Fig 4Example of IED related EEG-fMRI maps.
Patient with epilepsy #30. Clinical information: 11 years old male; presumed epileptogenic region located in the right posterior quadrant (circled in red). No structural lesion. Interictal and ictal epileptic activity arising from right posterior quadrant. Seizure semiology lateralizes to the right with involvement of the temporal lobe. EEG-fMRI showed significant BOLD signal changes in the posterior hippocampus, para hippocampal gyrus and fusiform gyrus. Section A shows an example of the activity in the presumed epileptogenic region during video and rest sessions. Section B shows an example of the activity in the presumed epileptogenic region during 2 sessions versus 4 sessions.