Investigation of outer cortical magnetisation transfer ratio abnormalities in multiple sclerosis clinical subgroups

Rebecca S Samson1, Manuel J Cardoso2, Nils Muhlert3

  • 1NMR Research Unit, UCL Institute of Neurology, London, UK r.samson@ucl.ac.uk.

Multiple Sclerosis (Houndmills, Basingstoke, England)
|February 21, 2014
PubMed
Abstract

Insights

Outer cortical magnetisation transfer ratio (MTR) is reduced in multiple sclerosis (MS) patients, particularly in secondary progressive MS (SPMS). This finding suggests significant outer cortical pathology in SPMS, aligning with post-mortem observations.

Area of Science:

  • Neuroimaging
  • Neurology
  • Radiology

Background:

  • Multiple Sclerosis (MS) is characterized by demyelination and neuronal loss in the outer cortex.
  • Investigating in vivo evidence of these cortical abnormalities is crucial for understanding MS progression.

Purpose of the Study:

  • To investigate in vivo evidence of outer cortical abnormalities in multiple sclerosis (MS) patients.
  • To measure the magnetisation transfer ratio (MTR) in different MS subgroups and healthy controls.

Main Methods:

  • Studied 44 relapsing-remitting (RRMS), 25 secondary progressive (SPMS), 19 primary progressive (PPMS) MS patients, and 35 healthy controls.
  • Acquired 3D T1-weighted images and MTR data, segmenting the cortex into outer and inner bands to calculate MTR values.

Main Results:

  • Outer cortical MTR was lower than inner cortical MTR in all groups (p<0.001).
  • SPMS and RRMS patients showed decreased outer cortical MTR compared to controls (p<0.001 and p<0.01, respectively).
  • SPMS patients exhibited the lowest outer cortical MTR, significantly lower than PPMS and RRMS patients (p<0.01).

Conclusions:

  • Lower outer cortical MTR in controls may indicate natural myelin content variations.
  • The significantly reduced outer cortical MTR in SPMS suggests extensive subpial pathology, including demyelination and neuronal loss.
  • Findings support the use of MTR to assess outer cortical pathology in MS, especially in SPMS.