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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Smouldering disease in paediatric-onset multiple sclerosis
Massimo Filippi1, Monica Margoni2, Brenda Banwell3
1Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy; Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy; Neurorehabilitation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy; Vita-Salute San Raffaele University, Milan, Italy; Neurophysiology Service, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Abstract:
Smouldering disease in multiple sclerosis (MS) refers to chronic central nervous system processes that occur beyond acute inflammation, driving long-term disability. Although current therapies effectively reduce relapse rates and MRI lesions, many individuals experience progression independent of relapse activity. While clinical progression is uncommon during childhood or adolescence, growing evidence suggests that subclinical progressive disease biology is already active even in this young age group, warranting early intervention to preserve function. Conventional MRI, while critical for diagnosis, lacks sensitivity for subtle damage. Advanced MRI techniques, including detection of chronic active lesions, global and focal brain damage, hold promise for early identification. Fluid biomarkers, such as neurofilament light chain and glial fibrillary acidic protein, provide non-invasive measures of neuroaxonal injury and ongoing chronic inflammation. This review summarises the role of MRI and fluid biomarkers in detecting smouldering disease in paediatric-onset MS and their application in supporting therapeutic decision-making.
Insights
Smouldering disease in paediatric multiple sclerosis (MS) shows early subclinical activity. Advanced MRI and fluid biomarkers can detect this chronic damage, guiding early intervention to preserve function.
Area of Science:
- Neurology
- Neuroimmunology
- Radiology
Background:
- Smouldering disease in multiple sclerosis (MS) involves chronic central nervous system processes contributing to long-term disability.
- While current MS therapies manage acute inflammation and lesions, many patients experience progression unrelated to relapses.
- Subclinical smouldering disease biology is active even in paediatric-onset MS, necessitating early intervention.
Purpose of the Study:
- To review the role of MRI and fluid biomarkers in detecting smouldering disease in paediatric-onset MS.
- To discuss the application of these detection methods in therapeutic decision-making for young MS patients.
Main Methods:
- Review of advanced Magnetic Resonance Imaging (MRI) techniques for detecting chronic active lesions and subtle brain damage.
- Analysis of fluid biomarkers, including neurofilament light chain and glial fibrillary acidic protein, as indicators of neuroaxonal injury and inflammation.
Main Results:
- Conventional MRI has limitations in detecting subtle, smouldering damage in MS.
- Advanced MRI techniques offer improved sensitivity for identifying chronic active lesions and overall brain damage.
- Fluid biomarkers provide non-invasive measures of ongoing neuroaxonal damage and inflammation.
Conclusions:
- Advanced MRI and fluid biomarkers are crucial for detecting subclinical smouldering disease in paediatric MS.
- Early identification of smouldering disease is essential for timely therapeutic intervention to preserve neurological function.
- These tools can support informed therapeutic decisions in managing paediatric-onset MS.
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