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Macroscopic and microscopic assessments of disease burden by MRI in multiple sclerosis: relationship to clinical

C Gasperini1, M A Horsfield, J W Thorpe

  • 1Multiple Sclerosis NMR Research Group, National Hospital, London.

Insights

Macroscopic white matter lesions, not microscopic changes in normal-appearing white matter, significantly contribute to disability in multiple sclerosis (MS) patients. Visible lesion volume strongly correlates with expanded disability status score (EDSS).

Area of Science:

  • Neuroimaging
  • Neurology
  • Radiology

Background:

  • Multiple sclerosis (MS) is characterized by white matter lesions.
  • Understanding the contribution of macroscopic lesions versus microscopic abnormalities in normal-appearing white matter (NAWM) to disability is crucial.

Purpose of the Study:

  • To evaluate the relative contributions of macroscopic white matter lesions and microscopic abnormalities in NAWM to disability progression in MS patients.
  • To compare total lesion volume (TLV) with T2 and texture analysis of NAWM as predictors of disability.

Main Methods:

  • Acquired dual echo T2-weighted SE images from 41 MS patients (various subtypes) and 10 controls.
  • Measured total visible lesion volume (TLV) using semiautomated detection.
  • Analyzed T2 and texture parameters in frontal NAWM.

Main Results:

  • NAWM T2 was significantly longer in MS patients than controls (P = .02).
  • No significant differences in texture parameters between patients and controls.
  • Mean TLV varied by MS subtype, highest in SPMS.
  • Significant correlation found between TLV and expanded disability status score (EDSS) (P < .01).
  • No significant correlation between NAWM T2 or texture and EDSS.

Conclusions:

  • Diffuse microscopic changes exist in MS NAWM, but texture analysis may be limited by image resolution.
  • Macroscopic lesions (TLV) are more critical than microscopic NAWM abnormalities in driving MS-related disability.
  • Visible lesion volume is a key predictor of disability in multiple sclerosis.

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