T1-based stratification of paramagnetic rim lesions in multiple sclerosis: Evidence of microstructural heterogeneity

Zhuowei Shi1, Huajiao Wang1, Zichun Yan1

  • 1Department of Radiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Multiple Sclerosis (Houndmills, Basingstoke, England)
|November 10, 2025
PubMed
Abstract

Insights

T1-intensity stratification effectively distinguishes paramagnetic rim lesion (PRL) heterogeneity in multiple sclerosis (MS). This classification correlates with distinct diffusion kurtosis metrics and clinical outcomes, supporting its utility in MS research.

Area of Science:

  • Neuroimaging
  • Radiology
  • Neurology

Background:

  • Paramagnetic rim lesions (PRLs) in multiple sclerosis (MS) display significant heterogeneity.
  • Understanding this heterogeneity is crucial for MS pathogenesis and treatment monitoring.

Purpose of the Study:

  • To determine if T1-intensity stratification can differentiate PRL heterogeneity.
  • To investigate the associations between PRL subtypes and clinical outcomes in MS patients.

Main Methods:

  • 112 MS patients were prospectively studied.
  • PRLs were classified into four subtypes based on T1-weighted black hole (BH) presence: PRL+BH+, PRL+BH-, PRL-BH+, PRL-BH-.
  • Diffusion kurtosis metrics, neurite density index (NDI), and magnetic susceptibility were analyzed. Associations with clinical outcomes (EDSS, SDMT, brain parenchymal volume) were assessed using generalized linear mixed-effects models.

Main Results:

  • PRL+BH+ lesions showed significantly lower kurtosis, NDI, and diamagnetic susceptibility compared to PRL+BH-.
  • PRL+BH+ volume positively correlated with higher Expanded Disability Status Scale (EDSS) scores and lower Symbol Digit Modalities Test (SDMT) scores and brain parenchymal volume.
  • Total PRL volume was associated with increased EDSS scores.

Conclusions:

  • T1-intensity-based stratification is a valuable tool for identifying heterogeneity within paramagnetic rim lesions in MS.
  • This approach reveals distinct microstructural properties and clinical associations for different PRL subtypes.