TY - JOUR
T1 - Characterization of children with early onset pediatric multiple sclerosis
AU - Kauth, Franziska
AU - Bertolini, Annikki
AU - Wendel, Eva Maria
AU - Koukou, Georgia
AU - Naggar, Ines El
AU - Chung, Jena
AU - Baumann, Matthias
AU - Schödl, Christopher
AU - Lechner, Christian
AU - Bigi, Sandra
AU - Blaschek, Astrid
AU - Hengstler, Jan Georg
AU - Schimmel, Mareike
AU - Nosadini, Margherita
AU - Sartori, Stefano
AU - Puthenparampil, Marco
AU - van's Gravesande, Karin Storm
AU - Drenckhahn, Anne
AU - Nikolaus, Marc
AU - Kauffmann, Birgit
AU - Thiels, Charlotte
AU - Häusler, Martin Georg
AU - Eckenweiler, Matthias
AU - Karenfort, Michael
AU - Marina, Adela Della
AU - Selek, Ayberk
AU - Öncel, Ibrahim
AU - Kornek, Barbara
AU - Reindl, Markus
AU - Rostásy, Kevin
N1 - Publisher Copyright:
© 2025 European Paediatric Neurology Society
PY - 2025/1
Y1 - 2025/1
N2 - 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.
AB - 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.
KW - Children
KW - Early onset pediatric MS
KW - Multiple sclerosis
KW - Pediatric
KW - Puberty
UR - https://www.scopus.com/pages/publications/85216076364
U2 - 10.1016/j.ejpn.2025.01.006
DO - 10.1016/j.ejpn.2025.01.006
M3 - Article
C2 - 39879856
AN - SCOPUS:85216076364
SN - 1090-3798
VL - 54
SP - 113
EP - 120
JO - European Journal of Paediatric Neurology
JF - European Journal of Paediatric Neurology
ER -