Widespread microstructural white matter involvement in amyotrophic lateral sclerosis: a whole-brain DTI study

M Cirillo1, F Esposito, G Tedeschi

  • 1Department of Neurological Sciences, Second University of Naples, Naples, Italy.

Abstract

Insights

This study reveals white matter degeneration in Amyotrophic Lateral Sclerosis (ALS) patients, particularly in the corpus callosum, correlating with upper motor neuron scores and disease progression beyond motor areas.

Area of Science:

  • Neuroimaging
  • Neurology
  • White Matter Diseases

Background:

  • Advanced MR imaging enhances understanding of ALS pathophysiology.
  • The full extent of neurodegeneration in ALS remains unclear.
  • Investigating white matter (WM) abnormalities is crucial for understanding ALS progression.

Purpose of the Study:

  • To detect WM microstructural abnormalities in ALS.
  • To analyze patterns within and beyond the corticospinal tract (CST).
  • To conduct a whole-brain analysis of pathological processes in ALS.

Main Methods:

  • Diffusion Tensor Imaging (DTI) was used.
  • 19 ALS patients and 20 healthy controls were included.
  • Whole-brain Tract-Based Spatial Statistics (TBSS) and region of interest (VOI) analyses were performed.

Main Results:

  • A significant decrease in fractional anisotropy (FA) was observed in the corpus callosum (CC) of ALS patients.
  • In the CC, decreased FA and increased radial diffusivity (RD) correlated with the upper motor neuron (UMN) score.
  • Positive correlations between FA and the ALS Functional Rating Scale-Revised (ALSFRS-R) were found in WM tracts under the left premotor cortex.

Conclusions:

  • WM degeneration in the CC is linked to pyramidal impairment in ALS.
  • Correlations suggest disease spread from motor to extramotor regions.
  • Findings highlight the role of WM abnormalities in ALS progression and extent.