Relationships of brain white matter microstructure with clinical and MR measures in relapsing-remitting multiple

Antonio Giorgio1, Jacqueline Palace, Heidi Johansen-Berg

  • 1Centre for Functional MRI of the Brain, University of Oxford, Oxford, UK.

Abstract

Insights

Diffusion tensor imaging (DTI) reveals localized white matter (WM) damage in multiple sclerosis (MS) patients, correlating with disability. Early disease progression in MS WM is not detectable with longitudinal DTI.

Area of Science:

  • Neuroimaging
  • Neurology
  • Biomedical Engineering

Background:

  • Multiple Sclerosis (MS) is a chronic autoimmune disease affecting the central nervous system.
  • Cerebral white matter (WM) damage is a hallmark of MS, impacting neurological function.
  • Diffusion Tensor Imaging (DTI) offers a non-invasive method to assess WM microstructure.

Purpose of the Study:

  • To investigate the relationship between DTI-derived WM microstructural integrity and clinical/MRI measures in relapsing-remitting MS (RR-MS).
  • To identify specific WM tracts affected by microstructural damage in early MS.
  • To explore the utility of DTI in tracking early disease progression.

Main Methods:

  • Study included 45 RR-MS patients with a median Expanded Disability Status Scale (EDSS) of 1.5 and disease duration of 3 years.
  • T2-lesion masks were generated, and voxelwise DTI analyses were performed using Tract-Based Spatial Statistics (TBSS).
  • Fractional anisotropy (FA) was analyzed in relation to T2-lesion volume (T2-LV) and EDSS scores.

Main Results:

  • Significant correlations were found between T2-lesion volume and FA in both lesions and normal-appearing white matter (NAWM).
  • Decreasing FA in the splenium of the corpus callosum (sCC) and pyramidal tract (PY) correlated with increasing EDSS scores.
  • FA changes were primarily attributed to increased perpendicular diffusivity, and no significant changes were observed over a 2-year follow-up.

Conclusions:

  • Microstructural damage, indicated by FA changes, is localized to specific WM tracts (sCC, PY) in early RR-MS and relates to clinical disability.
  • These FA alterations are driven by perpendicular diffusivity changes within both lesions and NAWM.
  • Longitudinal DTI measurements are not sensitive enough to monitor the early course of WM changes in MS patients.