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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
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Choroid plexus enlargement in secondary progressive MS: phenotype comparison.
Samuel Klistorner1, Michael H Barnett2, Chenyu Wang3
1Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia; Faculty of Medicine and Health Sciences, Macquarie University, Sydney, New South Wales, Australia.
Multiple Sclerosis and Related Disorders
|November 14, 2025
Summary
Choroid plexus volume increases with multiple sclerosis (MS) progression, particularly in secondary progressive MS (SPMS). This enlargement, linked to inflammation and tissue damage, may serve as a key biomarker for MS.
Area of Science:
- Neuroimmunology
- Neuroimaging
- Biomarker Discovery
Background:
- The choroid plexus (CP) is implicated in chronic inflammation in multiple sclerosis (MS).
- CP enlargement is noted in early MS, but its role in secondary progressive MS (SPMS) remains unclear.
- Understanding CP volume changes is crucial for MS progression insights.
Purpose of the Study:
- Quantify CP volume in SPMS patients.
- Compare CP volume across MS phenotypes (CIS, RRMS, SPMS).
- Assess CP volume associations with MS disease severity and progression.
Main Methods:
- Manual segmentation and normalization of CP volumes in 121 MS patients (CIS, RRMS, SPMS).
- Age correction using a healthy control cohort (n=109).
- Cross-sectional and longitudinal analyses of CP volume, ventricular size, lesion burden, and brain atrophy.
Main Results:
- Significant CP volume increase across MS phenotypes: SPMS showed 32% higher than CIS and 25% higher than RRMS.
- CP enlargement in SPMS was independent of ventricular size.
- Baseline CP volume correlated significantly with chronic lesion expansion (r²=0.33) and brain volume loss (r²=0.51) in SPMS.
Conclusions:
- CP enlargement is a progressive feature of MS, distinct from ventricular expansion.
- In SPMS, CP enlargement may indicate ongoing inflammation and contribute to tissue damage.
- CP volume shows potential as a biomarker for MS progression and inflammation.
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