Pathological correlates of magnetic resonance imaging texture heterogeneity in multiple sclerosis

Yunyan Zhang1, G R Wayne Moore, Cornelia Laule

  • 1Department of Radiology, University of Calgary, Calgary, Alberta; Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta; Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta.

Annals of Neurology
|August 14, 2013
PubMed
Abstract

Insights

Magnetic resonance imaging (MRI) texture analysis reveals greater heterogeneity in multiple sclerosis (MS) lesions and diffusely abnormal white matter (DAWM) compared to normal-appearing white matter (NAWM). This heterogeneity correlates with myelin and axonal loss, indicating MRI texture

Area of Science:

  • Neuroimaging
  • Neuropathology
  • Quantitative MRI

Background:

  • Multiple sclerosis (MS) is a demyelinating disease characterized by white matter lesions and diffuse abnormalities.
  • Accurate assessment of tissue pathology in MS using in vivo imaging remains challenging.
  • Histopathological hallmarks include myelin and axonal loss, and inflammation.

Purpose of the Study:

  • To analyze T2-weighted magnetic resonance imaging (MRI) texture in postmortem multiple sclerosis (MS) brains.
  • To correlate MRI texture features with specific tissue pathologies, including myelin and axonal integrity and inflammation.
  • To evaluate the potential of MRI texture analysis as a measure of tissue integrity in MS.

Main Methods:

  • Postmortem brain samples from 3 subjects with MS were analyzed.
  • Histological assessment involved Luxol fast blue (myelin) and Bielschowsky (axon) staining, and CD45+ cell counting for inflammation.
  • Regions of interest (lesions, diffusely abnormal white matter [DAWM], normal-appearing white matter [NAWM]) were matched between histology and T2-weighted MRI.
  • MRI texture was computed using polar Stockwell transform and statistically compared to histological findings.

Main Results:

  • Texture heterogeneity was significantly greater in MS lesions and DAWM compared to NAWM (p < 0.001).
  • Inflammation (CD45+ cells) was elevated in lesions and DAWM versus NAWM.
  • MRI texture heterogeneity showed a gradient within lesions and independently correlated with myelin density (p < 0.01), and with myelin and axonal density in most samples (p < 0.01).

Conclusions:

  • Texture analysis of T2-weighted MRI can quantify tissue alterations in MS.
  • Increased MRI texture heterogeneity is associated with more severe myelin and axonal pathology.
  • This technique shows potential as a non-invasive biomarker for tissue integrity in multiple sclerosis.

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