Radiologically isolated syndrome in children: Clinical and radiologic outcomes. Issue 6 (November 2017)
- Record Type:
- Journal Article
- Title:
- Radiologically isolated syndrome in children: Clinical and radiologic outcomes. Issue 6 (November 2017)
- Main Title:
- Radiologically isolated syndrome in children
- Authors:
- Makhani, Naila
Lebrun, Christine
Siva, Aksel
Brassat, David
Carra Dallière, Clarisse
de Seze, Jérôme
Du, Wei
Durand Dubief, Françoise
Kantarci, Orhun
Langille, Megan
Narula, Sona
Pelletier, Jean
Rojas, Juan Ignacio
Shapiro, Eugene D.
Stone, Robert T.
Tintoré, Mar
Uygunoglu, Ugur
Vermersch, Patrick
Wassmer, Evangeline
Okuda, Darin T.
Pelletier, Daniel - Abstract:
- Abstract : Objective: To describe clinical and radiologic outcomes of children with incidental findings on neuroimaging suggestive of CNS demyelination (termed "radiologically isolated syndrome" or RIS). Methods: Clinical and radiologic data were obtained from a historical cohort of children with no symptoms of demyelinating disease who had MRI scans that met the 2010 MRI criteria for dissemination in space for MS. Results: We identified 38 children (27 girls and 11 boys) with RIS now being prospectively followed at 16 sites in 6 countries. The mean follow-up time was 4.8 ± 5.3 years. The most common reason for initial neuroimaging was headache (20/38, 53%). A first clinical event consistent with CNS demyelination occurred in 16/38 children (42%; 95% confidence interval [CI]: 27%–60%) in a median of 2.0 years (interquartile range [IQR] 1.0–4.3 years). Radiologic evolution developed in 23/38 children (61%; 95% CI: 44%–76%) in a median of 1.1 years (IQR 0.5–1.9 years). The presence of ≥2 unique oligoclonal bands in CSF (hazard ratio [HR] 10.9, 95% CI: 1.4–86.2, p = 0.02) and spinal cord lesions on MRI (HR 7.8, 95% CI: 1.4–43.6, p = 0.02) were associated with an increased risk of a first clinical event after adjustment for age and sex. Conclusions: We describe the clinical characteristics and outcomes of children with incidental MRI findings highly suggestive of CNS demyelination. Children with RIS had a substantial risk of subsequent clinical symptoms and/or radiologicAbstract : Objective: To describe clinical and radiologic outcomes of children with incidental findings on neuroimaging suggestive of CNS demyelination (termed "radiologically isolated syndrome" or RIS). Methods: Clinical and radiologic data were obtained from a historical cohort of children with no symptoms of demyelinating disease who had MRI scans that met the 2010 MRI criteria for dissemination in space for MS. Results: We identified 38 children (27 girls and 11 boys) with RIS now being prospectively followed at 16 sites in 6 countries. The mean follow-up time was 4.8 ± 5.3 years. The most common reason for initial neuroimaging was headache (20/38, 53%). A first clinical event consistent with CNS demyelination occurred in 16/38 children (42%; 95% confidence interval [CI]: 27%–60%) in a median of 2.0 years (interquartile range [IQR] 1.0–4.3 years). Radiologic evolution developed in 23/38 children (61%; 95% CI: 44%–76%) in a median of 1.1 years (IQR 0.5–1.9 years). The presence of ≥2 unique oligoclonal bands in CSF (hazard ratio [HR] 10.9, 95% CI: 1.4–86.2, p = 0.02) and spinal cord lesions on MRI (HR 7.8, 95% CI: 1.4–43.6, p = 0.02) were associated with an increased risk of a first clinical event after adjustment for age and sex. Conclusions: We describe the clinical characteristics and outcomes of children with incidental MRI findings highly suggestive of CNS demyelination. Children with RIS had a substantial risk of subsequent clinical symptoms and/or radiologic evolution. The presence of oligoclonal bands in CSF and spinal cord lesions on MRI were associated with an increased risk of a first clinical event. … (more)
- Is Part Of:
- Neurology. Volume 4:Issue 6(2017)
- Journal:
- Neurology
- Issue:
- Volume 4:Issue 6(2017)
- Issue Display:
- Volume 4, Issue 6 (2017)
- Year:
- 2017
- Volume:
- 4
- Issue:
- 6
- Issue Sort Value:
- 2017-0004-0006-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-11
- Subjects:
- Neuroimmunology -- Periodicals
Neurology -- Periodicals
616.8 - Journal URLs:
- http://nn.neurology.org/ ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1212/NXI.0000000000000395 ↗
- Languages:
- English
- ISSNs:
- 2332-7812
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.502260
British Library DSC - BLDSS-3PM
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- 6060.xml