Back to Search
Start Over
Silent findings: Examination of asymptomatic demyelination in a pediatric US cohort.
- Source :
- Multiple Sclerosis & Related Disorders; Mar2023, Vol. 71, pN.PAG-N.PAG, 1p
- Publication Year :
- 2023
-
Abstract
- • Children may present with imaging findings of demyelination. • In our cohort, ⅓ had a clinical attack and ¾ developed new MRI activity. • Predictors for disease activity may include sex and juxtacortical lesion count. • T1 hypointense and infratentorial lesions may predict delayed progression. • Current MS and RIS diagnostic criteria may not be sufficient predictive tools. Limited data is available on children with evidence of silent central nervous system demyelination on MRI. We sought to characterize the population in a US cohort and identify predictors of clinical and radiologic outcomes. We identified 56 patients such patients who presented with incidental MRI findings suspect for demyelination, enrolled through our US Network of Pediatric Multiple Sclerosis Centers, and conducted a retrospective review of 38 patients with MR images, and examined risk factors for development of first clinical event or new MRI activity. MRI were rated based on published MS and radiologically isolated syndrome (RIS) imaging diagnostic criteria. One-third had a clinical attack and ¾ developed new MRI activity over a mean follow-up time of 3.7 years. Individuals in our cohort shared similar demographics to those with clinically definite pediatric-onset MS. We show that sex, presence of infratentorial lesions, T1 hypointense lesions, juxtacortical lesion count, and callosal lesions were predictors of disease progression. Interestingly, the presence of T1 hypointense and infratentorial lesions typically associated with worse outcomes were instead predictive of delayed disease progression on imaging in subgroup analysis. Additionally, currently utilized diagnostic criteria (both McDonald 2017 and RIS criteria) did not provide statistically significant benefit in risk stratification. Our findings underscore the need for further study to determine if criteria currently used for pediatric patients with purely radiographic evidence of demyelination are sufficient. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 22110348
- Volume :
- 71
- Database :
- Supplemental Index
- Journal :
- Multiple Sclerosis & Related Disorders
- Publication Type :
- Academic Journal
- Accession number :
- 162847940
- Full Text :
- https://doi.org/10.1016/j.msard.2023.104573