Impact of paramagnetic rim lesions on disability and race in multiple sclerosis: mediation analysis

Nara M Michaelson1, Sandra H Rúa2, Ulrike W Kaunzner1

  • 1Department of Neurology, Weill Cornell Medicine, New York, New York, USA.

Abstract

Insights

Black American multiple sclerosis (MS) patients have more severe disability, partly because they have a higher proportion of paramagnetic rim lesions (PRLs). These chronic active lesions significantly impact disability outcomes in this population.

Area of Science:

  • Neurology
  • Radiology
  • Immunology

Background:

  • Multiple sclerosis (MS) disproportionately affects Black American (BA) patients, who experience greater disability compared to White American (WA) patients.
  • The underlying reasons for this race-related disparity in MS disability remain incompletely understood.

Purpose of the Study:

  • To investigate the role of paramagnetic rim lesions (PRLs), a marker of chronic active lesions, in the increased disability observed in Black American MS patients.
  • To explore PRLs as a potential mediator of the relationship between race and MS disability.

Main Methods:

  • Retrospective observational study comparing BA and WA MS patients.
  • Identification of PRLs using Quantitative Susceptibility Mapping (QSM) MRI.
  • Causal mediation analysis to assess the impact of PRLs on race-related disability (Expanded Disability Status Scale - EDSS).

Main Results:

  • PRLs were more prevalent in BA MS patients (55%) than WA MS patients (39%).
  • A higher percentage of white matter lesions were PRLs in BA patients (8.01%) compared to WA patients (3.4%).
  • PRLs mediated 14% of the association between being BA and experiencing greater MS disability, even after controlling for covariates.

Conclusions:

  • Black American MS patients experience greater disability, with a higher proportion of paramagnetic rim lesions contributing significantly to this disparity.
  • This finding highlights the critical role of chronic active lesions, specifically PRLs, in driving disability outcomes in minority MS populations.