Evidence map›Paper›PMID 39243465›Full record

ArticleEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society2024

Impact of autoantibodies against myelin oligodendrocyte glycoprotein in paediatric acquired demyelinating disease: Intellectual functioning and academic performance.

Daniel Griffiths-King, Charly Billaud, Lydiah Makusha, Ling Lynette Looi, Evangeline Wassmer, Sukhvir Wright, Amanda G Wood

Abstract read
In one paragraph

Article in European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Daniel Griffiths-KingInstitute of Health and Neurodevelopment, College of Health and Life Sciences, Aston University, Birmingham, UK. Electronic address: d.griffiths-king@aston.ac.uk.
Charly BillaudInstitute of Health and Neurodevelopment, College of Health and Life Sciences, Aston University, Birmingham, UK; Nanyang Technological University, Singapore, Singapore.
Lydiah MakushaDepartment of Neurology, Birmingham Children's Hospital, Birmingham Women's and Children's Hospital NHS Foundation Trust, Birmingham, UK.
Ling Lynette LooiInstitute of Health and Neurodevelopment, College of Health and Life Sciences, Aston University, Birmingham, UK; Nanyang Technological University, Singapore, Singapore.
Evangeline WassmerInstitute of Health and Neurodevelopment, College of Health and Life Sciences, Aston University, Birmingham, UK; Department of Neurology, Birmingham Children's Hospital, Birmingham Women's and Children's Hospital NHS Foundation Trust, Birmingham, UK.
Sukhvir WrightInstitute of Health and Neurodevelopment, College of Health and Life Sciences, Aston University, Birmingham, UK; Department of Neurology, Birmingham Children's Hospital, Birmingham Women's and Children's Hospital NHS Foundation Trust, Birmingham, UK.
Amanda G WoodInstitute of Health and Neurodevelopment, College of Health and Life Sciences, Aston University, Birmingham, UK; School of Psychology, Faculty of Health, Melbourne Burwood Campus, Deakin University, Geelong, Victoria, Australia.

Funding

Wellcome Trust 216613
6 · The paper itself

Abstract

Paediatric acquired demyelinating syndromes (pADS) attack white matter pathways in the brain during an important period of development. Affected children can experience poor functional outcomes, including deficits in specific cognitive domains. Understanding risk factors for poor outcome will guide clinical management of these children. One clinical phenotype which may differentially impact cognitive outcomes is the presence of autoantibodies to myelin oligodendrocyte glycoprotein (MOG). Preliminary research has suggested that cognitive difficulties exist in paediatric patients who test positive for MOG antibodies or MOGAD (Myelin Oligodendrocyte Glycoprotein Associated Disease) however, they experience a less severe profile compared to seronegative counterparts. The current study assesses children diagnosed with pADS who tested positive or negative for MOG-ab using standardised assessments of both intellectual functioning and academic ability. The results show that a subset of MOGAD patients experience clinically significant sequalae in intellectual functioning and academic ability. The neuropsychological profile also differed between children with and without MOG-ab positivity, with seronegative patients more likely to show a clinically relevant difficulties at the individual patient level. Whilst no differences existed at the group-level; the current study demonstrates the relative additional risk of intellectual/academic difficulty associated with MOG-ab seronegativity. This research further supports the growing perspective that MOG-positivity confers a more favourable neuropsychological outlook than is the case for their seronegative counterparts. This broadening consensus offers reassurance for clinicians, families, and patients.

Indexed as

AutoantibodiesMyelin-Oligodendrocyte GlycoproteinAcademic PerformanceAdolescentChildChild, PreschoolDemyelinating DiseasesFemaleHumansIntelligenceMaleNeuropsychological TestsAutoantibodiesMOG protein, humanMyelin-Oligodendrocyte GlycoproteinAcquired demyelinating syndromesIntellectual functioningMOGADMyelin oligodendrocyte glycoprotein autoantibodiesOutcomesPediatric

Identifiers

PMID39243465
PMCPMC7618078

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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.