Evidence map›Paper›PMID 32255537›Full record

ArticleJournal of neuroimaging : official journal of the American Society of Neuroimaging2020

Constructing an Axonal-Specific Myelin Developmental Graph and its Application to Childhood Absence Epilepsy.

Gerhard S Drenthen, Eric L A Fonseca Wald, Walter H Backes, Albert P Aldenkamp, R Jeroen Vermeulen, Mariette H J A Debeij-van Hall, Sylvia Klinkenberg, Jacobus F A Jansen

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuroimaging : official journal of the American Society of Neuroimaging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 2 institutions in 1 country.

Gerhard S DrenthenSchool for Mental Health and Neuroscience, Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.ORCID 0000-0002-7708-8501
Eric L A Fonseca WaldSchool for Mental Health and Neuroscience, Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.
Walter H BackesSchool for Mental Health and Neuroscience, Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.
Albert P AldenkampSchool for Mental Health and Neuroscience, Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.
R Jeroen VermeulenSchool for Mental Health and Neuroscience, Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.
Mariette H J A Debeij-van HallDepartment of Behavioral Sciences, Epilepsy Center Kempenhaeghe, Sterkselseweg 65, Heeze, The Netherlands.
Sylvia KlinkenbergSchool for Mental Health and Neuroscience, Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.
Jacobus F A JansenSchool for Mental Health and Neuroscience, Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.
Maastricht University Medical Centre · NLKempenhaeghe · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThe process of myelination starts in utero around 20 weeks of gestation and continues through adulthood. We first set out to characterize the maturation of the tract-specific myelin content in healthy subjects from childhood (7-12 years) into adulthood (18-32 years). Second, we apply the resulting development graph to children with childhood absence epilepsy (CAE), a pediatric epilepsy that was previously characterized by changes in myelin content.

methodsIn a prospective cross-sectional study, 15 healthy children (7-12 years), 14 healthy adult participants (18-32 years) and 17 children with a clinical diagnosis of CAE (6-12 years) were included. For each participant, diffusion weighted images were acquired to reconstruct bundles of white matter tracts and multi-echo multi-slice GRASE images were acquired for myelin-water estimation. Subsequently, a tract-specific myelin development graph was constructed using the percentual difference in myelin-water content from childhood (12 year) to adulthood (25 year).

resultsThe graph revealed myelination patterns, where tracts in the central regions myelinate prior to peripheral tracts and intra-hemispheric tracts as well as tracts in the left hemisphere myelinate prior to inter-hemispheric tracts and tracts in the right hemisphere, respectively. No significant differences were found in myelin-water content between children with CAE and healthy children for neither the early developing tracts, nor the tracts that develop in a later stage. However, the difference between the myelin-water of late and early developing tracts is significantly smaller in the children with CAE.

conclusionThese results indicate that CAE is associated with widespread neurodevelopmental myelin differences.

Indexed as

AxonsMyelin SheathAdultChildCross-Sectional StudiesDiffusion Magnetic Resonance ImagingEpilepsy, AbsenceFemaleHumansMaleProspective StudiesWhite MatterYoung Adultdiffusion MRIMaturationmyelin-watertractographywhite matter

Identifiers

PMID32255537
PMCPMC7317939
OpenAlexW3015031534

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.