Evidence map›Paper›PMID 33395963›Full record

ArticleNeuroImage. Clinical2020

Modulation of epileptic networks by transient interictal epileptic activity: A dynamic approach to simultaneous EEG-fMRI.

G R Iannotti, M G Preti, F Grouiller, M Carboni, P De Stefano, F Pittau, S Momjian, D Carmichael, M Centeno, M Seeck and 4 more

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Evaluation of movement and brain activity.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2021
    Review
  5. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 3 countries.

G R IannottiEEG and Epilepsy, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland; Functional Brain Mapping Lab, Department of Fundamental Neurosciences, University of Geneva, Switzerland; Neurosurgery, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland. Electronic address: Giannina.Iannotti@unige.ch.
M G PretiInstitute of Bioengineering, Center for Neuroprosthetics, Ecole Polytechnique Federale de Lausanne (EPFL), Switzerland; Department of Radiology and Medical Informatics, University of Geneva, Geneva, Switzerland.
F GrouillerSwiss Center for Affective Sciences, University of Geneva, Switzerland; Laboratory of Behavioral Neurology and Imaging of Cognition, Department of Fundamental Neurosciences, University of Geneva, Switzerland.
M CarboniEEG and Epilepsy, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland; Functional Brain Mapping Lab, Department of Fundamental Neurosciences, University of Geneva, Switzerland.
P De StefanoEEG and Epilepsy, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland.
F PittauEEG and Epilepsy, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland; Epilepsy Unit, Institution de Lavigny, Switzerland.
S MomjianNeurosurgery, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland.
D CarmichaelBiomedical Engineering Department, Kings College London, United Kingdom; Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, United Kingdom.
M CentenoDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, United Kingdom; Epilepsy Unit, Neurology Department, Clinica Universidad de Pamplona, Navarra, Spain.
M SeeckEEG and Epilepsy, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland.
C M KorffPediatric Neurology Unit, University Hospitals of Geneva, Geneva, Switzerland.
K SchallerNeurosurgery, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland.
D Van De VilleInstitute of Bioengineering, Center for Neuroprosthetics, Ecole Polytechnique Federale de Lausanne (EPFL), Switzerland; Department of Radiology and Medical Informatics, University of Geneva, Geneva, Switzerland.
S VulliemozEEG and Epilepsy, Clinical Neuroscience Department, University Hospital and Faculty of Medicine of Geneva, Switzerland.
University Hospital of Geneva · CHUniversity of Geneva · CHClinica Universidad de Navarra · ESÉcole Polytechnique Fédérale de Lausanne · CHInstitution de Lavigny · CHNational Hospital for Neurology and Neurosurgery · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epileptic networks, defined as brain regions involved in epileptic brain activity, have been mapped by functional connectivity in simultaneous electroencephalography and functional magnetic resonance imaging (EEG-fMRI) recordings. This technique allows to define brain hemodynamic changes, measured by the Blood Oxygen Level Dependent (BOLD) signal, associated to the interictal epileptic discharges (IED), which together with ictal events constitute a signature of epileptic disease. Given the highly time-varying nature of epileptic activity, a dynamic functional connectivity (dFC) analysis of EEG-fMRI data appears particularly suitable, having the potential to identify transitory features of specific connections in epileptic networks. In the present study, we propose a novel method, defined dFC-EEG, that integrates dFC assessed by fMRI with the information recorded by simultaneous scalp EEG, in order to identify the connections characterised by a dynamic profile correlated with the occurrence of IED, forming the dynamic epileptic subnetwork. Ten patients with drug-resistant focal epilepsy were included, with different aetiology and showing a widespread (or multilobar) BOLD activation, defined as involving at least two distinct clusters, located in two different lobes and/or extended to the hemisphere contralateral to the epileptic focus. The epileptic focus was defined from the IED-related BOLD map. Regions involved in the occurrence of interictal epileptic activity; i.e., forming the epileptic network, were identified by a general linear model considering the timecourse of the fMRI-defined focus as main regressor. dFC between these regions was assessed with a sliding-window approach. dFC timecourses were then correlated with the sliding-window variance of the IED signal (VarIED), to identify connections whose dynamics related to the epileptic activity; i.e., the dynamic epileptic subnetwork. As expected, given the very different clinical picture of each individual, the extent of this subnetwork was highly variable across patients, but was but was reduced of at least 30% with respect to the initially identified epileptic network in 9/10 patients. The connections of the dynamic subnetwork were most commonly close to the epileptic focus, as reflected by the laterality index of the subnetwork connections, reported higher than the one within the original epileptic network. Moreover, the correlation between dFC timecourses and VarIED was predominantly positive, suggesting a strengthening of the dynamic subnetwork associated to the occurrence of IED. The integration of dFC and scalp IED offers a more specific description of the epileptic network, identifying connections strongly influenced by IED. These findings could be relevant in the pre-surgical evaluation for the resection or disconnection of the epileptogenic zone and help in reaching a better post-surgical outcome. This would be particularly important for patients characterised by a widespread pathological brain activity which challenges the surgical intervention.

Indexed as

EpilepsyMagnetic Resonance ImagingBrainBrain MappingElectroencephalographyHumansDynamic functional connectivityEEG-fMRIEpilepsyPre-surgical planning

Identifiers

PMID33395963
PMCPMC7645285
OpenAlexW3093225676

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.