Clinical and MRI substrates of Symbol Digit Modalities Test impairment in multiple sclerosis patients with an adult- and late-onset

Mult Scler. 2026 Mar;32(3):289-301. doi: 10.1177/13524585261417265. Epub 2026 Feb 23.

Abstract

Background: Multiple sclerosis (MS) onset occurs at diverse ages. Age of onset impact on clinical, brain MRI, and cognitive profiles remains unclear. We investigated the substrates of Symbol Digit Modalities Test (SDMT) impairment in patients with late-onset MS (LOMS) (⩾45 years) compared to adult-onset MS (AOMS) (<45 years).

Methods: 294 AOMS and 80 LOMS patients with disease duration of maximum 6 years from symptom onset and 519 healthy controls were retrospectively included from a multicenter MAGNIMS data set. We assessed between-group differences and correlates of SDMT impairment measuring lesion volume (LV), atrophy, global, intra- and inter-hemispheric structural connectivity and disconnection indices.

Results: 38% LOMS were impaired on SDMT compared to 39% AOMS (p = 0.751). LOMS showed higher LV (FDR-p = 0.018), gray matter (GM) atrophy (FDR-p = 0.050), intra- and inter-hemispheric disconnection compared to AOMS (all FDR-p < 0.028). Furthermore, LOMS showed higher modularity (FDR-p = 0.018) and decreased density (FDR-p < 0.001). Substrates of SDMT impairment were intra-hemispheric disconnection, LV, clustering coefficient, mean strength and efficiency (AUC = 0.730) in AOMS and commissural ratio and GM atrophy (AUC = 0.760) in LOMS.

Conclusions: Substrates contributing to SDMT impairment differ between these two distinct cohorts, being primarily driven by network dysfunction in AOMS and neurodegenerative processes in LOMS.

Keywords: Multiple sclerosis; cognitive impairment; late-onset multiple sclerosis; structural connectivity.

Publication types

  • Multicenter Study

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Atrophy / pathology
  • Cognitive Dysfunction* / diagnostic imaging
  • Cognitive Dysfunction* / etiology
  • Cognitive Dysfunction* / pathology
  • Cognitive Dysfunction* / physiopathology
  • Female
  • Gray Matter* / diagnostic imaging
  • Gray Matter* / pathology
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Multiple Sclerosis* / complications
  • Multiple Sclerosis* / diagnostic imaging
  • Multiple Sclerosis* / pathology
  • Multiple Sclerosis* / physiopathology
  • Retrospective Studies