Differentiating white matter lesions in multiple sclerosis and migraine using monoexponential and biexponential diffusion measurements

J Magn Reson Imaging. 2015 Mar;41(3):676-83. doi: 10.1002/jmri.24580. Epub 2014 Feb 14.

Abstract

Purpose: To compare the white matter lesions seen in multiple sclerosis and migraine using monoexponential and high b-value biexponential diffusion measurements.

Materials and methods: Diffusion-weighted images were acquired on a 3.0-Tesla magnetic resonance imaging system. Diffusion parameters were estimated using monoexponential (0-1000 s/mm(2) ) and biexponential (0-5000 s/mm(2) ) approaches from 15 multiple sclerosis patients, 15 patients with migraine and 15 healthy control subjects. The study was performed in accordance with the approval of the Regional Research Ethics Committee. The apparent diffusion coefficient (ADC) values were measured in the lesions and the normal-appearing white matter of patients and in the white matter of controls.

Results: High lesional ADCmono values were detected in both patient groups without significant differences between the groups (10.72 and 9.86 × 10(-4) mm(2) /s for MS and migraine respectively, P = 0.2134). The biexponential measurements showed significantly higher ADCfast , ADCslow , and Pslow values in the migraine lesions than in the multiple sclerosis lesions (16.47 versus 14.29, 1.41 versus 0.76, and 20.34 versus 12.01 all values in 10(-4) mm(2) /s; P = 0.0344, P = 0.0019, P = 0.0021, respectively).

Conclusion: Biexponential diffusion analysis may help to differentiate multiple sclerosis-related white matter lesions from migraine-related ones.

Keywords: brain white matter lesion; migraine; monoexponential and biexponential diffusion analysis; multiple sclerosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Diffusion Magnetic Resonance Imaging*
  • Female
  • Humans
  • Imaging, Three-Dimensional
  • Male
  • Migraine Disorders / pathology*
  • Multiple Sclerosis / pathology*
  • Prospective Studies
  • Reproducibility of Results
  • White Matter / pathology*