Evidence map›Paper›PMID 30895423›Full record

ArticleBrain topography2019

MEG Assessment of Expressive Language in Children Evaluated for Epilepsy Surgery.

Elaine Foley, J Helen Cross, Ngoc J Thai, A Richard Walsh, Peter Bill, Paul Furlong, Amanda G Wood, Antonella Cerquiglini, Stefano Seri

Open access · hybridAbstract read
In one paragraph

Article in Brain topography, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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  8. Pediatric Magnetoencephalography in Clinical Practice and Research.Neuroimaging clinics of North America · 2020
    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

9 authors at 5 institutions in 3 countries.

Elaine FoleyAston Brain Centre, School of Life and Health Sciences, Aston University, Birmingham, UK.
J Helen CrossDevelopmental Neurosciences Programme, Institute of Child Health, University College London, London, UK.
Ngoc J ThaiCRICBristol, Bristol's Clinical Research and Imaging Centre, Bristol, UK.
A Richard WalshChildren's Epilepsy Surgery Service, Birmingham Children's and Women's Hospital NHS Foundation Trust, Birmingham, UK.
Peter BillChildren's Epilepsy Surgery Service, Birmingham Children's and Women's Hospital NHS Foundation Trust, Birmingham, UK.
Paul FurlongAston Brain Centre, School of Life and Health Sciences, Aston University, Birmingham, UK.
Amanda G WoodAston Brain Centre, School of Life and Health Sciences, Aston University, Birmingham, UK.
Antonella CerquigliniDevelopmental Neuropsychiatry Section, Dipartimento di Scienze e BiotecnologieMedico-Chirurgiche, "Sapienza" Universita' di Roma Polo Pontino, Latina, Italy.
Stefano SeriAston Brain Centre, School of Life and Health Sciences, Aston University, Birmingham, UK. s.seri@aston.ac.uk.ORCID 0000-0002-9247-8102
Aston University · GBBirmingham Women’s and Children’s NHS Foundation Trust · GBAt Bristol · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Establishing language dominance is an important step in the presurgical evaluation of patients with refractory epilepsy. In the absence of a universally accepted gold-standard non-invasive method to determine language dominance in the preoperative assessment, a range of tools and methodologies have recently received attention. When applied to pediatric age, many of the proposed methods, such as functional magnetic resonance imaging (fMRI), may present some challenges due to the time-varying effects of epileptogenic lesions and of on-going seizures on maturational phenomena. Magnetoencephalography (MEG) has the advantage of being insensitive to the distortive effects of anatomical lesions on brain microvasculature and to differences in the metabolism or vascularization of the developing brain and also provides a less intimidating recording environment for younger children. In this study we investigated the reliability of lateralized synchronous cortical activation during a verb generation task in a group of 28 children (10 males and 18 females, mean age 12 years) with refractory epilepsy who were evaluated for epilepsy surgery. The verb generation task was associated with significant decreases in beta oscillatory power (13-30 Hz) in frontal and temporal lobes. The MEG data were compared with other available presurgical non-invasive data including cortical stimulation, neuropsychological and fMRI data on language lateralization where available. We found that the lateralization of MEG beta power reduction was concordant with language dominance determined by one or more different assessment methods (i.e. cortical stimulation mapping, neuropsychological, fMRI or post-operative data) in 89% of patients. Our data suggest that qualitative hemispheric differences in task-related changes of spectral power could offer a promising insight into the contribution of dominant and non-dominant hemispheres in language processing and may help to characterize the specialization and lateralization of language processes in children.

Indexed as

Functional LateralityLanguageAdolescentBrainBrain MappingChildDrug Resistant EpilepsyFemaleFrontal LobeHumansMagnetic Resonance ImagingMagnetoencephalographyMaleNeurosurgical ProceduresReproducibility of ResultsTemporal LobeBeamformersChildrenEpilepsy surgeryFunctional mappingHemispheric dominanceLanguage lateralizationMagnetoencephalography

Identifiers

PMID30895423
PMCPMC6476853
OpenAlexW2924796375

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.