Structural MRI signature of late- versus adult-onset multiple sclerosis: a multiparametric study

Nicolò Tedone1,2, Paolo Preziosa1,3,2, Elisabetta Pagani1

  • 1Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Abstract

Insights

Late-onset multiple sclerosis (LOMS) patients show greater white matter lesion burden and regional gray matter atrophy than adult-onset MS (AOMS) patients, despite similar disease duration. This suggests a more severe structural MRI profile in LOMS, potentially due to combined MS and aging effects.

Area of Science:

  • Neuroimaging
  • Neurology
  • Multiple Sclerosis Research

Background:

  • Structural MRI differences between late-onset multiple sclerosis (LOMS; onset ≥ 50 years) and adult-onset MS (AOMS) are not fully understood.
  • Tissue damage distribution and its relationship with clinical and cognitive outcomes in LOMS versus AOMS require further characterization.

Purpose of the Study:

  • To compare the structural MRI characteristics of LOMS and AOMS patients using a multiparametric approach.
  • To include age-matched healthy control (HC) groups for comparison.
  • To investigate the associations between MRI findings and clinical/cognitive measures.

Main Methods:

  • 3 Tesla MRI and clinical-cognitive assessments were performed on 40 LOMS patients, 195 AOMS patients, and 175 age-matched HC.
  • Analyses included white matter (WM) lesion volume (T2-LV) and distribution, volumetric measures, tract-based spatial statistics, and voxel-based morphometry.
  • Voxel-wise analyses examined group differences and correlations with disease duration (DD), Expanded Disability Status Scale (EDSS), and Symbol Digit Modalities Test (SDMT).

Main Results:

  • Both MS groups exhibited higher T2-LV, widespread WM abnormalities, and reduced total, gray matter (GM), and deep GM volumes compared to HC.
  • LOMS patients showed significantly higher lesion frequency in the left superior longitudinal fasciculus (SLF) compared to AOMS patients.
  • An interaction effect revealed higher T2-LV and more pronounced regional GM atrophy in motor-insular-subcortical areas in LOMS versus AOMS.

Conclusions:

  • LOMS patients demonstrate a higher T2-hyperintense white matter lesion burden and more significant regional gray matter atrophy than AOMS patients.
  • These differences persist despite similar disease duration and lack of global gray matter volume differences, suggesting a distinct structural MRI profile in LOMS.
  • The findings may reflect a combination of MS-related damage and age-related processes contributing to a more severe structural MRI phenotype in LOMS.