Evidence map›Paper›PMID 42545102›Full record

ArticleEuropean journal of neurology2026

Update on the Incidence of Paediatric Multiple Sclerosis, Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease, Aquaporin-4 Antibody-Positive Neuromyelitis Optica Spectrum Disorder, and Other Acquired Demyelinating Syndromes in the Netherlands, 2017-2025, Including the COVID-19 Pandemic.

Sandy Molenaar, Michiel S J Buijze, Arlette L Bruijstens, Yu Yi M Wong, Maud A Quist, C Louk de Mol, Beatrijs H A Wokke, Rinze F Neuteboom, Dutch Study Group for Paediatric Multiple Sclerosis and Acute Disseminated Encephalomyelitis

Abstract read
In one paragraph

Article in European journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

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5 · Who and what money

Authors and funding

9 authors.

Sandy MolenaarDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-0432-0138
Michiel S J BuijzeDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-2875-5304
Arlette L BruijstensDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-7990-5894
Yu Yi M WongDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-8828-4487
Maud A QuistMS Center ErasMS, Erasmus University Medical Centre, Rotterdam, the Netherlands.
C Louk de MolDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, the Netherlands.
Beatrijs H A WokkeDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-2616-8464
Rinze F NeuteboomDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0001-6136-4981
Dutch Study Group for Paediatric Multiple Sclerosis and Acute Disseminated Encephalomyelitis

Funding

PostcodeloterijStichting MS Research
6 · The paper itself

Abstract

backgroundAcquired demyelinating syndromes (ADS) in children include multiple sclerosis (MS), myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), aquaporin 4 antibody-positive neuromyelitis optica spectrum disorder (AQP4+ NMOSD), and other seronegative disorders. We previously reported an increased incidence of overall paediatric ADS and MS between 2007 to 2010 and 2011-2016 (from 0.66 to 0.80 and 0.15 to 0.26 per 100,000 person-years, respectively). Environmental factors, including viral exposure, may influence these rates. Comparing a recent period that includes the COVID-19 pandemic provides an opportunity to study temporal patterns.

methodsChildren < 18 years with a first demyelinating event between January 2017 and June 2025 were prospectively included in the nationwide PROUDkids 2.0 study or referred to the Dutch Paediatric MS Centre. Diagnoses followed international criteria, and incidence rates were calculated using national population data.

resultsAmong 257 included children, 111 (43%) had MS, 93 (36%) MOGAD, 5 (2%) AQP4+ NMOSD, and 48 (19%) seronegative ADS. Overall ADS incidence was 0.91 per 100,000 person-years, with MS 0.40, MOGAD 0.33, AQP4+ NMOSD 0.02, and seronegative ADS 0.16 per 100,000 person-years. Compared with 2011-2016 (0.26 per 100,000), MS incidence increased, whereas other ADS rates remained stable. MS incidence declined after COVID-19 restrictions, particularly among adolescents, while MOGAD incidence rose modestly in younger children during the COVID restrictions.

conclusionsPaediatric MS incidence continues to rise in the Netherlands, whereas the incidence of other ADS remains stable. Temporal variations in the incidence of MS and MOGAD during and after the COVID-19 pandemic may reflect the influence of viral exposure in their pathogenesis.

Indexed as

Aquaporin 4COVID-19Multiple SclerosisMyelin Oligodendrocyte Glycoprotein Antibody-Associated DiseaseNeuromyelitis OpticaAdolescentChildChild, PreschoolDemyelinating Autoimmune Diseases, CNSFemaleHumansIncidenceInfantMaleMyelin-Oligodendrocyte GlycoproteinNetherlandsAQP4 protein, humanAquaporin 4Myelin-Oligodendrocyte Glycoproteincentral nervous system demyelinating diseaseschildCOVID‐19incidencemultiple sclerosis

Identifiers

PMID42545102
PMCPMC13431134

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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.