Longitudinal Persistence of Meningeal Enhancement on Postcontrast 7T 3D-FLAIR MRI in Multiple Sclerosis

S N Jonas1, I Izbudak2, A A Frazier3

  • 1From the Department of Radiology (S.N.J., A.A.F.), University of Maryland Medical Center, Baltimore, Maryland samueljonas@umm.edu.

Abstract

Insights

Meningeal enhancement in multiple sclerosis (MS) on 7T MRI scans persists over time, varying by pattern and correlating with increased disability. Persistence did not differ based on treatment or disease phenotype.

Area of Science:

  • Neurology
  • Radiology
  • Medical Imaging

Background:

  • Preliminary research suggests 7-tesla (7T) 3D-FLAIR MRI with postgadolinium contrast is valuable for detecting meningeal abnormalities in multiple sclerosis (MS).
  • The longitudinal persistence of this meningeal enhancement has not been systematically studied.

Purpose of the Study:

  • To investigate the longitudinal persistence of meningeal enhancement in MS using 7T 3D-FLAIR MRI.
  • To determine if persistence varies by enhancement pattern, treatment status, disease phenotype, or disability score.

Main Methods:

  • Prospective scanning of 31 MS subjects at two time points, approximately one year apart, with some scanned a second year later.
  • Categorization of enhancement foci into four subtypes: subarachnoid spread/fill, subarachnoid nodular, vessel wall, and dural.
  • Comparison of enhancement persistence with demographic and clinical variables.

Main Results:

  • Persistence ranged from 71% to 100% at 1 year and 73% to 100% at 2 years, depending on the enhancement pattern.
  • Subarachnoid subtypes persisted less frequently than vessel wall and dural subtypes.
  • Persistence did not significantly differ between treated/untreated or progressive/non-progressive MS groups, but correlated with worsening Expanded Disability Status Scale scores.

Conclusions:

  • Longitudinal persistence of meningeal enhancement on 7T 3D-FLAIR MRI in MS varies by enhancement pattern.
  • Persistence correlates with worsening disability but is not significantly influenced by treatment status or disease phenotype.

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