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Cognitive Ability in Pediatric-Onset Multiple Sclerosis: A Case Series
Maria Ballarà Petitbò1, Borja Esteso Orduña2, Elena Oyaga de Frutos1
1Department of Neurology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Insights
Pediatric-onset multiple sclerosis (POMS) can impair cognitive function, particularly in younger children. Early, high-efficacy treatment like Fingolimod may improve cognitive outcomes in pediatric patients with MS.
Area of Science:
- Neurology
- Pediatrics
- Neuroimmunology
Background:
- Pediatric-onset multiple sclerosis (POMS) affects children during critical neurodevelopmental periods, increasing vulnerability to neurological damage and cognitive decline.
- Cognitive function is a key concern in POMS, necessitating identification of prognostic factors and effective treatments.
Purpose of the Study:
- To analyze cognitive and clinical characteristics in children with POMS.
- To identify factors influencing cognitive performance and treatment outcomes in POMS.
Main Methods:
- Retrospective descriptive study of pediatric patients with POMS (2010-2023).
- Analysis of neuropsychological assessments, clinical data, and radiological findings.
Main Results:
- Cognitive function showed overall improvement, nearing significance in visual perceptual organization and hand dexterity.
- Earlier disease onset and younger assessment age correlated with poorer nonverbal skills.
- Higher relapse rates, disability scores, lesion burden, and basal ganglia involvement predicted worse cognitive performance.
- Fingolimod therapy and longer treatment duration were linked to better cognitive outcomes.
Conclusions:
- Younger children with POMS face higher risks of cognitive impairment, especially early in the disease.
- Clinical and radiological factors can predict cognitive deficits.
- Early initiation of high-efficacy disease-modifying therapies like Fingolimod is associated with improved cognitive prognosis.
Background:
Pediatric-onset multiple sclerosis (POMS) emerges during a crucial stage of neurodevelopment, conferring special vulnerability to neurological damage and cognitive decline. This underscores the importance of addressing cognitive domain and identifying its prognostic factors and treatment.
Methods:
Retrospective descriptive study of a cohort of children with POMS in a tertiary pediatric hospital from 2010 to 2023. Cognitive and clinical characteristics during neuropsychological assessments were analyzed.
Results:
Twelve patients were included (average disease onset 11.5 years). Cognitive assessments showed an overall improvement, being close to statistical significance in visual perceptual organization and speed/accuracy of the dominant hand. Earlier disease onset and younger age at the time of assessment were associated with worse nonverbal skills. A higher number of relapses, Expanded Disability Status Scale score, increased lesion burden, and basal ganglia involvement were significantly correlated with worse cognitive performance in multiple domains. Fingolimod therapy and longer treatment duration were related to better cognitive outcomes.
Conclusions:
Children with POMS presenting at a younger age are at increased risk of cognitive impairment, especially during the early stages of the disease. Some clinical and radiological factors can predict worse intellectual performance, while high-efficacy disease-modifying treatment like Fingolimod and its precocious initiation is associated with better cognitive prognosis.
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