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Childhood multiple sclerosis is associated with reduced brain volumes at first clinical presentation and brain growth
Frederik Bartels1, Katharina Nobis2, Graham Cooper3
1Department of Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany/ Berlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany.
Insights
Brain volume loss in paediatric multiple sclerosis (pedMS) is evident at initial diagnosis and worsens over two years. This brain atrophy correlates with disease activity, suggesting MRI volume changes as a potential outcome measure.
Area of Science:
- Neurology
- Radiology
- Paediatric Medicine
Background:
- Paediatric multiple sclerosis (pedMS) is associated with reduced brain volumes and impaired brain growth.
- The exact timing of brain volume loss onset in pedMS is not well understood.
Purpose of the Study:
- To longitudinally investigate brain volumes in a multi-centre European cohort of pedMS patients.
- To assess brain volume changes at first presentation and after a 2-year follow-up period.
Main Methods:
- Utilized high-resolution MRI data from 37 pedMS patients at initial presentation and 2-year follow-up.
- Compared patient MRI data with matched longitudinal data from the NIH Paediatric MRI Data Repository.
Main Results:
- PedMS patients exhibited reduced whole brain, grey matter, and white matter volumes, with increased ventricular volumes compared to controls at both time points.
- Over two years, patients showed significant reductions in whole brain and white matter volumes and increased ventricular volume.
- Brain volume loss at follow-up correlated with infratentorial lesions, relapses, and higher EDSS scores.
Conclusions:
- Brain volume loss in pedMS is present at initial clinical presentation and accelerates over two years.
- Increased disease activity is linked to more severe brain volume loss.
- MRI-based brain volume changes may serve as a valuable outcome parameter in future pedMS studies.
Background:
Paediatric multiple sclerosis (pedMS) patients at a single site were shown to have reduced brain volumes and failure of age-expected brain growth compared to healthy controls. However, the precise time of onset of brain volume loss remains unclear.
Objective:
To longitudinally study brain volumes in a multi-centre European cohort at first presentation and after 2 years.
Methods:
Brain volumes of high-resolution magnetic resonance imaging (MRI) data from 37 pedMS patients at first presentation prior to steroid therapy and at 2-year follow-up ( n = 21) were compared to matched longitudinal MRI data from the NIH Paediatric MRI Data Repository.
Results:
Patients showed significantly reduced whole brain, grey and white matter and increased ventricular volumes at initial presentation and at follow-up compared to controls. Over 2 years, patients exhibited significant reduction of whole brain and white matter volumes, accompanied by increased ventricular volume. Brain volume loss at follow-up correlated with a higher number of infratentorial lesions, relapses and an increased Expanded Disability Status Scale (EDSS) score.
Conclusions:
In pedMS patients, brain volume loss is present already at first clinical presentation and accelerated over 2 years. Increased disease activity is associated with more severe brain volume loss. MRI brain volume change might serve as an outcome parameter in future prospective pedMS studies.
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