Paramagnetic rim lesions lead to pronounced diffuse periplaque white matter damage in multiple sclerosis

Nik Krajnc1, Victor Schmidbauer2, Joel Leinkauf2

  • 1Department of Neurology, Medical University of Vienna, Vienna, Austria/Comprehensive Center for Clinical Neurosciences and Mental Health, Medical University of Vienna, Vienna, Austria/Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

Multiple Sclerosis (Houndmills, Basingstoke, England)
|September 15, 2023
PubMed
Abstract

Insights

Paramagnetic rim lesions (PRLs) in multiple sclerosis (MS) show longer T1 relaxation times, indicating more severe tissue damage compared to other lesion types. Evaluating the area around these lesions may predict silent disease progression in people with MS.

Area of Science:

  • Neuroimaging
  • Radiology
  • Multiple Sclerosis Research

Background:

  • Paramagnetic rim lesions (PRLs) are an established imaging biomarker in multiple sclerosis (MS).
  • PRLs are associated with more severe disease progression and disability in people with MS (pwMS).

Purpose of the Study:

  • To quantitatively assess magnetic resonance imaging (MRI) metrics of PRLs, diffuse susceptibility-weighted imaging (SWI)-hypointense lesions (DSHLs), and SWI-isointense lesions (SILs).
  • To evaluate the periplaque area (PPA) surrounding these lesions and normal-appearing white matter (NAWM) in pwMS.
  • To correlate MRI metrics with different MS subtypes.

Main Methods:

  • A cross-sectional study involving 30 pwMS.
  • Quantitative MRI metrics were acquired using a multi-dynamic multi-echo (MDME) sequence and processed with SyMRI software.
  • Analysis included T1 relaxation times for lesions, PPA, and NAWM.

Main Results:

  • PRLs exhibited significantly longer T1 relaxation times compared to DSHLs and SILs (p < 0.001).
  • The PPA surrounding PRLs showed longer T1 relaxation times than the PPA of SILs and NAWM (p < 0.001).
  • Patients with secondary progressive MS (SPMS) had longer T1 relaxation times in PRLs and their PPA compared to relapsing forms of MS (p=0.015 and p=0.013, respectively).

Conclusions:

  • PRLs are associated with more extensive white matter damage than SILs.
  • Quantitative MRI evaluation of the PRL PPA may serve as a valuable biomarker for detecting silent disease progression in pwMS.

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