Evidence map›Paper›PMID 31920937›Full record

ArticleFrontiers in neurology2019

Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal Spikes.

Anna Elisabetta Vaudano, Pietro Avanzini, Gaetano Cantalupo, Melissa Filippini, Andrea Ruggieri, Francesca Talami, Elisa Caramaschi, Patrizia Bergonzini, Aglaia Vignoli, Pierangelo Veggiotti and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Sleep and Epilepsy Link by Plasticity.Frontiers in neurology · 2020
    Article
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

19 authors at 7 institutions in 1 country.

Anna Elisabetta VaudanoNeurology Unit, OCB Hospital, AOU Modena, Modena, Italy.
Pietro AvanziniItalian National Research Council, Parma Research Unit, Parma, Italy.
Gaetano CantalupoChild Neuropsychiatry, University of Verona, Verona, Italy.
Melissa FilippiniChild Neuropsychiatry Unit, IRCCS, Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.
Andrea RuggieriDepartment of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Francesca TalamiDepartment of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Elisa CaramaschiPediatric Neurology Unit, AOU Modena, Modena, Italy.
Patrizia BergonziniPediatric Neurology Unit, AOU Modena, Modena, Italy.
Aglaia VignoliDepartment of Health Sciences, University of Milano, Milan, Italy.
Pierangelo VeggiottiPediatric Neurology Unit, V. Buzzi Hospital, University of Milan, Milan, Italy.
Azzura GuerraPhysical Medicine and Rehabilitation Unit, Sant'Andrea Hospital, University of Rome La Sapienza, Rome, Italy.
Giuliana GessaroliDepartment of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Margherita SantucciChild Neuropsychiatry Unit, IRCCS, Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.
Maria Paola CaneviniPediatric Neurology Unit, AOU Modena, Modena, Italy.
Benedetta PiccoloChild Neuropsychiatry, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Francesco PisaniChild Neuropsychiatry, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Giuseppe GobbiChild Neuropsychiatry Unit, IRCCS, Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.
Bernardo Dalla BernardinaChild Neuropsychiatry, University of Verona, Verona, Italy.
Stefano MelettiNeurology Unit, OCB Hospital, AOU Modena, Modena, Italy.
University of Modena and Reggio Emilia · ITAzienda Unita' Sanitaria Locale Di Modena · ITInstitute of Neurological Sciences · ITUniversity of Milan · ITUniversity of Parma · ITUniversity of Verona · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Childhood epilepsy with centrotemporal spikes (CECTS) is the most common type of "self-limited focal epilepsies." In its typical presentation, CECTS is a condition reflecting non-lesional cortical hyperexcitability of rolandic regions. The benign evolution of this disorder is challenged by the frequent observation of associated neuropsychological deficits and behavioral impairment. The abundance (or frequency) of interictal centrotemporal spikes (CTS) in CECTS is considered a risk factor for deficits in cognition. Herein, we captured the hemodynamic changes triggered by the CTS density measure (i.e., the number of CTS for time bin) obtained in a cohort of CECTS, studied by means of video electroencephalophy/functional MRI during quite wakefulness. We aim to demonstrate a direct influence of the diurnal CTS frequency on epileptogenic and cognitive networks of children with CECTS. A total number of 8,950 CTS (range between 27 and 801) were recorded in 23 CECTS (21 male), with a mean number of 255 CTS/patient and a mean density of CTS/30 s equal to 10,866 ± 11.46. Two independent general linear model models were created for each patient based on the effect of interest: "individual CTS" in model 1 and "CTS density" in model 2. Hemodynamic correlates of CTS density revealed the involvement of a widespread cortical-subcortical network encompassing the sensory-motor cortex, the Broca's area, the premotor cortex, the thalamus, the putamen, and red nucleus, while in the CTS event-related model, changes were limited to blood-oxygen-level-dependent (BOLD) signal increases in the sensory-motor cortices. A linear relationship was observed between the CTS density hemodynamic changes and both disease duration (positive correlation) and age (negative correlation) within the language network and the bilateral insular cortices. Our results strongly support the critical role of the CTS frequency, even during wakefulness, to interfere with the normal functioning of language brain networks.

Indexed as

BOLDCECTScentrotemporal spikescognitionepileptic discharges frequencylanguage network

Identifiers

PMID31920937
PMCPMC6930928
OpenAlexW2995684793

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.