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Primary and transitional progressive MS: a clinical and MRI cross-sectional study.
V L Stevenson1, D H Miller, M Rovaris
1NMR Research Unit, Institute of Neurology, London, UK.
Neurology
|March 17, 1999
Summary
Primary progressive multiple sclerosis (PPMS) and transitional progressive (TP) MS patients exhibit distinct clinical and MRI characteristics compared to secondary progressive MS (SPMS). Atrophy measures correlate with disability, offering a promising avenue for monitoring disease progression in PPMS.
Area of Science:
- Neurology
- Neuroimmunology
- Radiology
Background:
- Ten percent of multiple sclerosis (MS) patients present with a progressive disease course from onset.
- A subset of these patients, transitional progressive (TP) MS, experience a single relapse.
- Both primary progressive (PPMS) and TPMS patients have historically been excluded from licensed MS treatments and clinical trials.
Purpose of the Study:
- To characterize the clinical and MRI features of a large cohort of PPMS and TPMS patients.
- To compare these features with a reference group of secondary progressive MS (SPMS) patients.
- To identify potential biomarkers for monitoring disease progression in progressive MS subtypes.
Main Methods:
- Recruitment of patients from six European centers.
- Clinical assessment including Expanded Disability Status Scale (EDSS) scoring.
- Brain and spinal cord MRI to evaluate lesion load and atrophy.
Main Results:
- PPMS patients were older at onset and had lower brain T2 and T1 lesion loads compared to SPMS patients.
- SPMS and TPMS cohorts showed more spinal cord T2 lesions than PPMS patients, with SPMS exhibiting greater atrophy.
- EDSS scores correlated with brain and spinal cord atrophy in PPMS and TPMS patients, but not with brain lesion load.
Conclusions:
- Monitoring PPMS progression is challenging, but atrophy measures show promise for correlation with EDSS.
- This study enhances understanding of unique progressive MS patient groups.
- Acquisition of serial data will further expand insights into these patient populations.