White and gray matter damage in primary progressive MS: The chicken or the egg?

Benedetta Bodini1, Declan Chard2, Daniel R Altmann2

  • 1From the Department of Neuroinflammation (B.B., D.C., D.R.A., D.T., D.H.M., A.J.T., C.W.-K., O.C.), Queen Square MS Centre, University College of London Institute of Neurology; Department of Neuroimaging (B.B.), Institute of Psychiatry, King's College London; London School of Hygiene and Tropical Medicine (D.R.A.), University of London; NIHR UCL/UCLH Biomedical Research Centre (D.H.M., A.J.T., O.C.), London, UK. benedetta.bodini@icm-institute.org.

Neurology
|December 18, 2015
PubMed
Abstract

Insights

In early primary progressive multiple sclerosis (PPMS), white matter (WM) lesions predict gray matter (GM) damage. This suggests WM pathology drives cortical changes in PPMS.

Area of Science:

  • Neuroimaging
  • Neurology
  • Multiple Sclerosis Research

Background:

  • Primary progressive multiple sclerosis (PPMS) is characterized by progressive neurological decline.
  • Understanding the temporal relationship between white matter (WM) and gray matter (GM) damage is crucial for PPMS progression.
  • Existing models propose either primary WM or GM damage initiating the disease cascade.

Purpose of the Study:

  • To investigate the temporal sequence of WM and GM damage in vivo in early PPMS.
  • To test the hypothesis that WM tract abnormalities precede cortical changes.
  • To test the hypothesis that cortical abnormalities precede WM tract changes.

Main Methods:

  • Magnetization transfer imaging (MTI) was used to assess WM and GM integrity in 47 early PPMS patients and 18 controls.
  • Imaging was performed at baseline and after 2 years in a subgroup of patients.
  • Tract-based and region-of-interest analyses were conducted to evaluate relationships between WM and GM damage.

Main Results:

  • Patients with PPMS showed lower MTR values in most regions compared to controls.
  • WM damage significantly predicted subsequent GM damage in motor and visual pathways.
  • Normal-appearing WM MTR at 2 years was associated with baseline lesion MTR in affected tracts.

Conclusions:

  • Findings support a primary WM damage model in early PPMS.
  • Cortical damage appears to be a consequence of underlying WM pathology.
  • Abnormalities within WM lesions are predictive of subsequent normal-appearing WM changes and downstream cortical damage.