Regional grey matter microstructural changes and volume loss according to disease duration in multiple sclerosis

Elisabeth Solana1, Eloy Martinez-Heras2, Victor Montal3,4

  • 1Center of Neuroimmunology, Laboratory of Advanced Imaging in Neuroimmunological Diseases, Hospital Clinic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) and Universitat de Barcelona, Barcelona, Spain. elisabeth.solana@idibaps.org.

Scientific Reports
|August 20, 2021
PubMed

Insights

Grey matter (GM) changes in multiple sclerosis (MS) progress over time, with distinct microstructural and volume alterations appearing early and becoming widespread in later disease stages, correlating with disability.

Area of Science:

  • Neuroimaging
  • Neurology
  • Medical Physics

Background:

  • Grey matter (GM) impairment in multiple sclerosis (MS) has poorly understood spatio-temporal characteristics.
  • Diffusion MRI and surface-based analysis offer novel approaches to investigate GM changes.

Purpose of the Study:

  • To investigate regional microstructural and volume modifications in GM in MS patients across different disease durations.
  • To explore the relationship between GM changes and disease severity.

Main Methods:

  • Utilized a surface-based diffusion MRI processing tool on 54 healthy controls and 247 MS patients (classified into MS1, MS2, MS3 based on disease duration).
  • Compared GM mean diffusivity (MD), fractional anisotropy (FA), and volume between groups.
  • Assessed clinical associations of GM changes with white matter lesion load and disability.

Main Results:

  • Regional diffusion (MD, FA) and volume changes showed no overlap early in MS but became widespread later.
  • Higher MD was observed in the MS1 group (temporal cortex), with volume loss in deep GM and left precuneus.
  • MS2 and MS3 groups exhibited progressive increases in MD and volume loss across more brain regions, with minor FA increases in specific areas.
  • GM alterations correlated with white matter lesion load and physical/cognitive disability.

Conclusions:

  • Microstructural integrity loss and atrophy in MS exhibit differential spatial patterns early on, accumulating over time.
  • Distinct pathogenic mechanisms likely underlie the observed tissue damage progression in MS.