Evidence map›Paper›PMID 26106575›Full record

ArticleNeuroImage. Clinical2015

What graph theory actually tells us about resting state interictal MEG epileptic activity.

Guiomar Niso, Sira Carrasco, María Gudín, Fernando Maestú, Francisco Del-Pozo, Ernesto Pereda

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Article in NeuroImage. Clinical, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

42 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Guiomar NisoCenter for Biomedical Technology, Technical University of Madrid, Madrid, Spain ; McConnell Brain Imaging Center, Montreal Neurological Institute, McGill University, Montreal, Canada.
Sira CarrascoTeaching General Hospital of Ciudad Real, Ciudad Real, Spain.
María GudínTeaching General Hospital of Ciudad Real, Ciudad Real, Spain.
Fernando MaestúCenter for Biomedical Technology, Technical University of Madrid, Madrid, Spain ; Biomedical Research Networking Center in Bioengineering Biomaterials and Nanomedicine (CIBER-BBN), Madrid, Spain.
Francisco Del-PozoCenter for Biomedical Technology, Technical University of Madrid, Madrid, Spain ; Biomedical Research Networking Center in Bioengineering Biomaterials and Nanomedicine (CIBER-BBN), Madrid, Spain.
Ernesto PeredaDept. of Industrial Engineering, Electrical Engineering and Bioengineering Group, Institute of Biomedical Technology (ITB-CIBICAN), University of La Laguna, Tenerife, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Graph theory provides a useful framework to study functional brain networks from neuroimaging data. In epilepsy research, recent findings suggest that it offers unique insight into the fingerprints of this pathology on brain dynamics. Most studies hitherto have focused on seizure activity during focal epilepsy, but less is known about functional epileptic brain networks during interictal activity in frontal focal and generalized epilepsy. Besides, it is not clear yet which measures are most suitable to characterize these networks. To address these issues, we recorded magnetoencephalographic (MEG) data using two orthogonal planar gradiometers from 45 subjects from three groups (15 healthy controls (7 males, 24 ± 6 years), 15 frontal focal (8 male, 32 ± 16 years) and 15 generalized epileptic (6 male, 27 ± 7 years) patients) during interictal resting state with closed eyes. Then, we estimated the total and relative spectral power of the largest principal component of the gradiometers, and the degree of phase synchronization between each sensor site in the frequency range [0.5-40 Hz]. We further calculated a comprehensive battery of 15 graph-theoretic measures and used the affinity propagation clustering algorithm to elucidate the minimum set of them that fully describe these functional brain networks. The results show that differences in spectral power between the control and the other two groups have a distinctive pattern: generalized epilepsy presents higher total power for all frequencies except the alpha band over a widespread set of sensors; frontal focal epilepsy shows higher relative power in the beta band bilaterally in the fronto-central sensors. Moreover, all network indices can be clustered into three groups, whose exemplars are the global network efficiency, the eccentricity and the synchronizability. Again, the patterns of differences were clear: the brain network of the generalized epilepsy patients presented greater efficiency and lower eccentricity than the control subjects for the high frequency bands, without a clear topography. Besides, the frontal focal epileptic patients showed only reduced eccentricity for the theta band over fronto-temporal and central sensors. These outcomes indicate that functional epileptic brain networks are different to those of healthy subjects during interictal stage at rest, with a unique pattern of dissimilarities for each type of epilepsy. Further, when properly selected, three network indices suffice to provide a comprehensive description of these differences. Yet, since such uniqueness in the pattern of differences is also evident in the power spectrum, we conclude that the added value of the graph theory approach in this context should not be overestimated.

Indexed as

AdultConnectomeCortical SynchronizationEpilepsy, Frontal LobeEpilepsy, GeneralizedFemaleHumansMagnetoencephalographyMaleMathematical ConceptsMiddle AgedNerve NetYoung AdultEpilepsyFC, functional connectivityFunctional connectivityGraph theoryMagnetoencephalographyMEG, magnetoencephalographyPhase synchronizationPLV, phase locking valuePS, phase synchronization

Identifiers

PMID26106575
PMCPMC4475779

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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.