Characterization of children with early onset pediatric multiple sclerosis

Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS. To investigate clinical, laboratory and imaging differences between children with early onset pediatric MS (<11 years, EOPMS) and late onset pediatric MS (≥11 years...

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Published inEuropean journal of paediatric neurology Vol. 54; pp. 113 - 120
Main Authors Kauth, Franziska, Bertolini, Annikki, Wendel, Eva-Maria, Koukou, Georgia, Naggar, Ines El, Chung, Jena, Baumann, Matthias, Schödl, Christopher, Lechner, Christian, Bigi, Sandra, Blaschek, Astrid, Hengstler, Jan Georg, Schimmel, Mareike, Nosadini, Margherita, Sartori, Stefano, Puthenparampil, Marco, van's Gravesande, Karin Storm, Drenckhahn, Anne, Nikolaus, Marc, Kauffmann, Birgit, Thiels, Charlotte, Häusler, Martin Georg, Eckenweiler, Matthias, Karenfort, Michael, Marina, Adela Della, Selek, Ayberk, Öncel, Ibrahim, Kornek, Barbara, Reindl, Markus, Rostásy, Kevin
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.01.2025
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Online AccessGet full text
ISSN1090-3798
1532-2130
1532-2130
DOI10.1016/j.ejpn.2025.01.006

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Abstract Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS. 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). 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. 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 %). 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. •EOPMS and LOPMS share important similarities but also important differences.•Presence of additional OCBs in the CSF was comparable in both age groups.•An EBV-infection does not seem to be mandatory for the development of MS in EOPMS.•Signs of brain tissue loss are already occurring in pre- and in post pubertal MS.
AbstractList Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS. 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). 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. 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 %). 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. •EOPMS and LOPMS share important similarities but also important differences.•Presence of additional OCBs in the CSF was comparable in both age groups.•An EBV-infection does not seem to be mandatory for the development of MS in EOPMS.•Signs of brain tissue loss are already occurring in pre- and in post pubertal MS.
Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS.BACKGROUNDEarly onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS.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).OBJECTIVETo investigate clinical, laboratory and imaging differences between children with early onset pediatric MS (<11 years, EOPMS) and late onset pediatric MS (≥11 years, LOPMS).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.METHODSMostly 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.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 %).RESULTSIn 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 %).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.CONCLUSIONOur 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.
Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS. 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). 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. 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 %). 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.
Author van's Gravesande, Karin Storm
Naggar, Ines El
Puthenparampil, Marco
Eckenweiler, Matthias
Baumann, Matthias
Hengstler, Jan Georg
Nosadini, Margherita
Kornek, Barbara
Schimmel, Mareike
Bigi, Sandra
Schödl, Christopher
Drenckhahn, Anne
Sartori, Stefano
Nikolaus, Marc
Thiels, Charlotte
Chung, Jena
Kauth, Franziska
Karenfort, Michael
Wendel, Eva-Maria
Öncel, Ibrahim
Reindl, Markus
Marina, Adela Della
Bertolini, Annikki
Kauffmann, Birgit
Blaschek, Astrid
Selek, Ayberk
Koukou, Georgia
Häusler, Martin Georg
Rostásy, Kevin
Lechner, Christian
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  organization: Department of Paediatrics, Kepler University Hospital Linz, Austria
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  givenname: Matthias
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  surname: Baumann
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  givenname: Christian
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  givenname: Sandra
  orcidid: 0000-0003-2158-2241
  surname: Bigi
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  organization: Division of Pediatric Neurology, Department of Pediatrics, Children's Hospital of Central Switzerland, Lucerne, Switzerland
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  givenname: Jan Georg
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  givenname: Marco
  surname: Puthenparampil
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  givenname: Karin Storm
  surname: van's Gravesande
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  organization: Department for Neuropediatrics and Muscle Disease, Medical Center - University of Freiburg, Faculty of Medicine, Freiburg, Germany and Department of Pediatrics, Child and Adolescent Psychosomatics, Technical University Munich, Munich, Germany
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  givenname: Anne
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  givenname: Marc
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  givenname: Birgit
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  givenname: Charlotte
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  organization: Department of Neuropediatrics and Socialpediatrics, University Hospital of Ruhr University Bochum, Bochum, Germany
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  givenname: Martin Georg
  orcidid: 0000-0002-8433-8919
  surname: Häusler
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  organization: Division of Neuropediatrics and Social Pediatrics, Department of Pediatrics, RWTH Aachen University Hospital, Aachen, Germany
– sequence: 23
  givenname: Matthias
  surname: Eckenweiler
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  organization: Department of Neuropediatrics and Muscle Disorders, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany
– sequence: 24
  givenname: Michael
  surname: Karenfort
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– sequence: 25
  givenname: Adela Della
  surname: Marina
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– sequence: 26
  givenname: Ayberk
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  orcidid: 0000-0003-2817-1402
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  givenname: Kevin
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  email: kevin.rostasy@uni-wh.de
  organization: Department of Pediatric Neurology, Children's Hospital Datteln, Witten/Herdecke University, Datteln, Germany
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Keywords Puberty
Multiple sclerosis
Early onset pediatric MS
Children
Pediatric
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Snippet Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS. To investigate clinical,...
Early onset pediatric multiple sclerosis (EOPMS) provides an early window of opportunity to understand the mechanisms leading to MS.BACKGROUNDEarly onset...
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StartPage 113
SubjectTerms Adolescent
Age of Onset
Child
Child, Preschool
Children
Early onset pediatric MS
Female
Humans
Magnetic Resonance Imaging
Male
Multiple sclerosis
Multiple Sclerosis - cerebrospinal fluid
Multiple Sclerosis - diagnostic imaging
Multiple Sclerosis - epidemiology
Multiple Sclerosis - pathology
Multiple Sclerosis - physiopathology
Oligoclonal Bands - cerebrospinal fluid
Pediatric
Prospective Studies
Puberty
Recurrence
Title Characterization of children with early onset pediatric multiple sclerosis
URI https://www.clinicalkey.com/#!/content/1-s2.0-S1090379825000066
https://dx.doi.org/10.1016/j.ejpn.2025.01.006
https://www.ncbi.nlm.nih.gov/pubmed/39879856
https://www.proquest.com/docview/3161520663
Volume 54
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