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Review
. 2025 Jul;22(4):e00631.
doi: 10.1016/j.neurot.2025.e00631. Epub 2025 Jun 27.

Pediatric multiple sclerosis: Improving outcome through high-efficacy therapies

Affiliations
Review

Pediatric multiple sclerosis: Improving outcome through high-efficacy therapies

Lama Saleh Aljomah et al. Neurotherapeutics. 2025 Jul.

Abstract

Pediatric-onset multiple sclerosis (POMS) refers to multiple sclerosis occurring in individuals under 18 years of age. It is characterized by poor cognitive outcomes and a more inflammatory course, more frequent clinical relapses, and a greater number of MRI lesions compared to adult-onset MS (AOMS). Prompt recognition of multiple sclerosis in this population is essential, as early intervention with disease-modifying therapies may change the trajectory of disease progression. In this paper, we will review diagnostic criteria for pediatric multiple sclerosis, differential diagnosis, and current and emerging therapeutic approaches. While a number of DMTs are approved for adult MS, few are approved for pediatric use. Many of these DMTs are used off-label, with real-world evidence demonstrating their effectiveness and safety. The review evaluates existing evidence for the use of these therapies in pediatric populations, with an emphasis on both existing clinical trials and real-world data that supports their use. In addition, we will briefly highlight ongoing clinical trials and emerging therapies for POMS.

Keywords: Demyelinating disease; Disease-modifying therapy; Pediatric-onset multiple sclerosis.

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Conflict of interest statement

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Fig. 1
Fig. 1
2017 Revised McDonald Criteria for Multiple Sclerosis.
Fig. 2
Fig. 2
Axial and Sagittal FLAIR MRI scans of the brain demonstrating high lesion load at presentation in a 14 year-old child with MS. Note the presence of multiple discrete hyperintense lesions involving the supratentorial white matter and posterior fossa, involving the cerebellar peduncles and the cerebellar hemispheres bilaterally.

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