Evidence map›Paper›PMID 27060092›Full record

ArticleBrain topography2016

MEG Coherence and DTI Connectivity in mTLE.

Mohammad-Reza Nazem-Zadeh, Susan M Bowyer, John E Moran, Esmaeil Davoodi-Bojd, Andrew Zillgitt, Barbara J Weiland, Hassan Bagher-Ebadian, Fariborz Mahmoudi, Kost Elisevich, Hamid Soltanian-Zadeh

Open access · greenAbstract read
In one paragraph

Article in Brain topography, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Exploring ASL perfusion MRI as a substitutive modality for 18F-FDG PET in determining the laterality of mesial temporal lobe epilepsy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
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  2. Article
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  4. Dynamic functional connectivity in temporal lobe epilepsy: a graph theoretical and machine learning approach.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Article
  5. Distinct patterns of hippocampal subfield volume loss in left and right mesial temporal lobe epilepsy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Article
  6. Article
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  8. Changes in White Matter Microstructure Impact Cognition by Disrupting the Ability of Neural Assemblies to Synchronize.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
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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

10 authors at 4 institutions in 2 countries.

Mohammad-Reza Nazem-ZadehResearch Administration, Henry Ford Health System, Detroit, MI, 48202, USA. mnazemz1@hfhs.org.
Susan M BowyerNeurology, Henry Ford Health System, Detroit, MI, 48202, USA.
John E MoranNeurology, Henry Ford Health System, Detroit, MI, 48202, USA.
Esmaeil Davoodi-BojdResearch Administration, Henry Ford Health System, Detroit, MI, 48202, USA.
Andrew ZillgittNeurology, Henry Ford Health System, Detroit, MI, 48202, USA.
Barbara J WeilandInstitute of Cognitive Science University of Colorado Boulder, Boulder, CO, 80309, USA.
Hassan Bagher-EbadianResearch Administration, Henry Ford Health System, Detroit, MI, 48202, USA.
Fariborz MahmoudiResearch Administration, Henry Ford Health System, Detroit, MI, 48202, USA.
Kost ElisevichDivision of Neurosurgery, Department of Clinical Neurosciences, Spectrum Health System, Michigan State University, Grand Rapids, MI, 49503, USA.
Hamid Soltanian-ZadehResearch Administration, Henry Ford Health System, Detroit, MI, 48202, USA.
Henry Ford Health System · USMichigan State University · USQazvin Islamic Azad University · IRUniversity of Colorado Boulder · US

Funding

Decision Support System for Temporal Lobe EpilepsyR01EB013227 · NIBIB · HENRY FORD HEALTH SYSTEM · PI SOLTANIAN-ZADEH, HAMID · 2012 to 2015
$1.7M
NIBIB NIH HHS R01 EB013227
6 · The paper itself

Abstract

Magnetoencephalography (MEG) is a noninvasive imaging method for localization of focal epileptiform activity in patients with epilepsy. Diffusion tensor imaging (DTI) is a noninvasive imaging method for measuring the diffusion properties of the underlying white matter tracts through which epileptiform activity is propagated. This study investigates the relationship between the cerebral functional abnormalities quantified by MEG coherence and structural abnormalities quantified by DTI in mesial temporal lobe epilepsy (mTLE). Resting state MEG data was analyzed using MEG coherence source imaging (MEG-CSI) method to determine the coherence in 54 anatomical sites in 17 adult mTLE patients with surgical resection and Engel class I outcome, and 17 age- and gender- matched controls. DTI tractography identified the fiber tracts passing through these same anatomical sites of the same subjects. Then, DTI nodal degree and laterality index were calculated and compared with the corresponding MEG coherence and laterality index. MEG coherence laterality, after Bonferroni adjustment, showed significant differences for right versus left mTLE in insular cortex and both lateral orbitofrontal and superior temporal gyri (p < 0.017). Likewise, DTI nodal degree laterality, after Bonferroni adjustment, showed significant differences for right versus left mTLE in gyrus rectus, insular cortex, precuneus and superior temporal gyrus (p < 0.017). In insular cortex, MEG coherence laterality correlated with DTI nodal degree laterality ([Formula: see text] in the cases of mTLE. None of these anatomical sites showed statistically significant differences in coherence laterality between right and left sides of the controls. Coherence laterality was in agreement with the declared side of epileptogenicity in insular cortex (in 82 % of patients) and both lateral orbitofrontal (88 %) and superior temporal gyri (88 %). Nodal degree laterality was also in agreement with the declared side of epileptogenicity in gyrus rectus (in 88 % of patients), insular cortex (71 %), precuneus (82 %) and superior temporal gyrus (94 %). Combining all significant laterality indices improved the lateralization accuracy to 94 % and 100 % for the coherence and nodal degree laterality indices, respectively. The associated variations in diffusion properties of fiber tracts quantified by DTI and coherence measures quantified by MEG with respect to epileptogenicity possibly reflect the chronic microstructural cerebral changes associated with functional interictal activity. The proposed methodology for using MEG and DTI to investigate diffusion abnormalities related to focal epileptogenicity and propagation may provide a further means of noninvasive lateralization.

Indexed as

Diffusion Tensor ImagingMagnetoencephalographyAdolescentAdultCerebral CortexEpilepsy, Temporal LobeFemaleFrontal LobeFunctional LateralityHumansMaleMiddle AgedParietal LobeTemporal LobeYoung AdultCoherenceConnectivityDiffusion tensor imagingFiber tractsMagnetoencephalographyMesial temporal lobe epilepsyNodal degree

Identifiers

PMID27060092
PMCPMC5542022
OpenAlexW2328666684

What OpenQuestion holds

Textmetadata
LicenceTDM
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.