Franziska Kauth, Annikki Bertolini, Eva-Maria Wendel, Georgia Koukou, Ines El Naggar, Jena Chung, Matthias Baumann, Christopher Schödl, Christian Lechner, Sandra Bigi, Astrid Blaschek, Jan Georg Hengstler, Mareike Schimmel, Margherita Nosadini, Stefano Sartori, Marco Puthenparampil, Karin Storm Van's Gravesande, Anne Drenckhahn, Marc Nikolaus, Birgit Kauffmann, Charlotte Thiels, Martin Georg Häusler, Matthias Eckenweiler, Michael Karenfort, Adela Della Marina, Ayberk Selek, Ibrahim Öncel, Barbara Kornek, Markus Reindl, Kevin Rostásy
{"title":"Characterization of children with early onset pediatric multiple sclerosis.","authors":"Franziska Kauth, Annikki Bertolini, Eva-Maria Wendel, Georgia Koukou, Ines El Naggar, Jena Chung, Matthias Baumann, Christopher Schödl, Christian Lechner, Sandra Bigi, Astrid Blaschek, Jan Georg Hengstler, Mareike Schimmel, Margherita Nosadini, Stefano Sartori, Marco Puthenparampil, Karin Storm Van's Gravesande, Anne Drenckhahn, Marc Nikolaus, Birgit Kauffmann, Charlotte Thiels, Martin Georg Häusler, Matthias Eckenweiler, Michael Karenfort, Adela Della Marina, Ayberk Selek, Ibrahim Öncel, Barbara Kornek, Markus Reindl, Kevin Rostásy","doi":"10.1016/j.ejpn.2025.01.006","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS.</p><p><strong>Objective: </strong>To investigate clinical, laboratory and imaging differences between children with early onset pediatric MS (<11 years, EOPMS) and late onset pediatric MS (≥11 years, LOPMS).</p><p><strong>Methods: </strong>Mostly prospectively collected data of children with MS including clinical presentation, MRI at onset, time to second relapse, relapse rate, treatment history, and CSF markers were eligible.</p><p><strong>Results: </strong>In total 274 children were included, n = 53 children with EOPMS and n = 221 children with LOPMS. In children with EOPMS both sexes were equally affected, while in LOPMS the female sex was more prevalent (p < 0.001). Presence of additional oligoclonal bands (OCBs) in the cerebrospinal fluid (CSF) was comparable in both age groups (92.3 % vs 89.5 %). Children with EOPMS had more relapses in the first 2 years (p = 0.004). Children with LOPMS had significantly more spinal lesions (p = 0.001). Presence of a prior EBV infection tested in a subset of children with EOPMS (n = 34) was only detected in 27/34 (79 %).</p><p><strong>Conclusion: </strong>Our findings suggest that both groups share important similarities but also important differences such as an increased relapse rate and a higher amount of infratentorial lesions in EOPMS. Furthermore, our results allude to a prior EBV-infection possibly not being an indispensable requirement for the development of MS in children with EOPMS.</p>","PeriodicalId":50481,"journal":{"name":"European Journal of Paediatric Neurology","volume":"54 ","pages":"113-120"},"PeriodicalIF":2.3000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Paediatric Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ejpn.2025.01.006","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS.
Objective: To investigate clinical, laboratory and imaging differences between children with early onset pediatric MS (<11 years, EOPMS) and late onset pediatric MS (≥11 years, LOPMS).
Methods: Mostly prospectively collected data of children with MS including clinical presentation, MRI at onset, time to second relapse, relapse rate, treatment history, and CSF markers were eligible.
Results: In total 274 children were included, n = 53 children with EOPMS and n = 221 children with LOPMS. In children with EOPMS both sexes were equally affected, while in LOPMS the female sex was more prevalent (p < 0.001). Presence of additional oligoclonal bands (OCBs) in the cerebrospinal fluid (CSF) was comparable in both age groups (92.3 % vs 89.5 %). Children with EOPMS had more relapses in the first 2 years (p = 0.004). Children with LOPMS had significantly more spinal lesions (p = 0.001). Presence of a prior EBV infection tested in a subset of children with EOPMS (n = 34) was only detected in 27/34 (79 %).
Conclusion: Our findings suggest that both groups share important similarities but also important differences such as an increased relapse rate and a higher amount of infratentorial lesions in EOPMS. Furthermore, our results allude to a prior EBV-infection possibly not being an indispensable requirement for the development of MS in children with EOPMS.
期刊介绍:
The European Journal of Paediatric Neurology is the Official Journal of the European Paediatric Neurology Society, successor to the long-established European Federation of Child Neurology Societies.
Under the guidance of a prestigious International editorial board, this multi-disciplinary journal publishes exciting clinical and experimental research in this rapidly expanding field. High quality papers written by leading experts encompass all the major diseases including epilepsy, movement disorders, neuromuscular disorders, neurodegenerative disorders and intellectual disability.
Other exciting highlights include articles on brain imaging and neonatal neurology, and the publication of regularly updated tables relating to the main groups of disorders.