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Glymphatic System May Mediate the Relation Between Choroid Plexus and Brain Damage in Multiple Sclerosis
Paolo Preziosa1,2,3, Elisabetta Pagani1, Monica Margoni1,2,4
1Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Neurology(R) Neuroimmunology & Neuroinflammation
|June 5, 2025
Summary
In multiple sclerosis (MS), enlarged choroid plexus (CP) volume is linked to brain damage, potentially by worsening glymphatic system dysfunction. This study shows glymphatic dysfunction mediates the relationship between CP enlargement and brain injury in MS patients.
Area of Science:
- Neuroimmunology
- Neuroimaging
- Cerebrospinal Fluid Dynamics
Background:
- The choroid plexus (CP) regulates brain immunity and cerebrospinal fluid (CSF) production, crucial for the glymphatic system.
- In multiple sclerosis (MS), CP enlargement and glymphatic dysfunction are observed but their relationship to brain damage is unclear.
Purpose of the Study:
- To investigate if glymphatic system dysfunction mediates the association between CP enlargement and brain damage in MS patients.
- To explore the link between CP volume, glymphatic function, and brain injury markers in MS.
Main Methods:
- MRI scans (FLAIR, T1-weighted, DWI, SWI) were acquired from 146 MS patients and 72 healthy controls (HC).
- Glymphatic function was assessed using the diffusion along the perivascular space (DTI-ALPS) index.
- Automated measurement of CP volume was performed.
Main Results:
- MS patients exhibited larger CP and white matter (WM) lesion volumes, and reduced DTI-ALPS index and brain volumes compared to HC.
- In MS, increased CP volume correlated with lower DTI-ALPS index and higher WM lesion volumes.
- The DTI-ALPS index partially mediated the association between normalized CP volume and WM lesion volumes, as well as normalized brain volumes.
Conclusions:
- Enlarged normalized CP volume in MS may contribute to brain damage.
- This contribution might occur through promoting a chronic proinflammatory state and mediating glymphatic system dysfunction.
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