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Updated: Jan 23, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Real-world detection of paramagnetic rim lesions and their association with disease burden in multiple sclerosis
Olavi Misin1, Anni Piispanen2, Markus Matilainen1
1Turku PET Centre, Turku University Hospital, University of Turku, and Åbo Akademi University, Turku, Finland; Neurocenter, Turku University Hospital, Turku, Finland; Clinical Neurosciences, University of Turku, Turku, Finland; InFLAMES Research Flagship, University of Turku, Turku, Finland.
Background:
Paramagnetic rim lesions (PRLs) are an emerging MRI biomarker in multiple sclerosis (MS). On susceptibility-sensitive MRI, PRLs are characterized by a paramagnetic shift at the lesion rim corresponding to iron-laden macrophages and microglia, and PRL detection can hence be viewed as a proxy for lesion-associated smoldering inflammation in MS brain. The aim of this study was to identify PRLs in a standard university hospital setting to explore the associations between PRL burden and MS-related clinical and paraclinical parameters.
Methods:
We retrospectively reviewed all 3T brain MRI studies performed as part of MS patient management at a tertiary university hospital in Finland between September 2021 and December 2023. PRLs were visually identified on filtered phase images from susceptibility-weighted imaging (SWI) sequences. Brain volumetric data were extracted from post-contrast 3D T1-weighted images using an automated quantification tool (cNeuro® cMRI). Clinical and laboratory variables were obtained by manual chart review from electronic medical records.
Results:
The final cohort included 206 patients. 34% of patients had at least one PRL (the PRL1+ group). The median number of PRLs in the PRL1+ group was 2 and the maximum number was 11. Within the PRL1+ group, PRL count correlated positively with Expanded Disability Status Scale (EDSS), Multiple Sclerosis Severity Score (MSSS) and T2 lesion volume. Patients with PRLs had significantly smaller thalami compared to those without PRLs.
Discussion:
Our real-world data reinforce evidence that PRLs are linked to more severe disease and demonstrate that PRL identification using manufacturer-reconstructed SWI filtered phase images provides a feasible imaging parameter to assess progression-associated pathology in MS in a standard clinical setting.
Insights
Paramagnetic rim lesions (PRLs) indicate ongoing inflammation in multiple sclerosis (MS). This study found that the presence and number of PRLs correlate with increased MS severity, disability, and brain volume loss.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- Paramagnetic rim lesions (PRLs) are an emerging MRI biomarker in multiple sclerosis (MS).
- PRLs reflect active, smoldering inflammation in the MS brain, characterized by iron-laden macrophages and microglia.
- Detecting PRLs can serve as a proxy for ongoing inflammatory processes in MS.
Purpose of the Study:
- To identify Paramagnetic Rim Lesions (PRLs) in a routine clinical setting.
- To investigate the association between PRL burden and clinical/paraclinical parameters in MS patients.
- To assess the feasibility of PRL identification for monitoring MS progression.
Main Methods:
- Retrospective review of 3T brain MRI scans from 206 MS patients (Sept 2021-Dec 2023).
- Visual identification of PRLs on susceptibility-weighted imaging (SWI) filtered phase images.
- Automated quantification of brain volumetric data and manual chart review for clinical variables.
Main Results:
- 34% of patients exhibited at least one PRL (PRL1+ group).
- PRL count positively correlated with Expanded Disability Status Scale (EDSS), Multiple Sclerosis Severity Score (MSSS), and T2 lesion volume.
- Patients with PRLs showed significantly smaller thalamic volumes compared to those without PRLs.
Conclusions:
- Real-world data confirm PRLs are associated with more severe MS.
- PRL identification using standard SWI filtered phase images is a feasible clinical tool.
- PRLs can serve as a valuable imaging parameter for assessing progression-associated pathology in MS.
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