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Updated: Dec 27, 2025

Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
Published on: February 19, 2021
Automated separation of diffusely abnormal white matter from focal white matter lesions on MRI in multiple sclerosis
Josefina Maranzano1, Mahsa Dadar2, Maryna Zhernovaia3
1Department of Anatomy, University of Quebec in Trois-Rivieres, Trois-Rivieres, Quebec, Canada; McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Background:
Previous histopathology and MRI studies have addressed the differences between focal white matter lesions (FWML) and diffusely abnormal white matter (DAWM) in multiple sclerosis (MS). These two categories of white matter T2-weighted (T2w) hyperintensity show different degrees of demyelination, axonal loss and immune cell density on histopathology, potentially offering distinct correlations with symptoms.
Objectives:
1) To automate the separation of FWML and DAWM using T2w MRI intensity thresholds and to investigate their differences in magnetization transfer ratios (MTR), which are sensitive to myelin content; 2) to correlate MTR values in FWML and DAWM with normalized signal intensity values on fluid attenuated inversion recovery (FLAIR), T2w, and T1-weighted (T1w) contrasts, as well as with the ratio of T2w/T1w normalized values, in order to determine whether these normalized intensities can be used when MTR is not available.
Methods:
We used three MRI datasets: datasets 1 and 2 had 20 MS participants each, scanned with similar 3T MRI protocols in 2 centers, including: 3D T1w (MP2RAGE), 3D FLAIR, 2D T2w, and 3D magnetization-transfer (MT) contrasts. Dataset 3 consisted of 67 scans of participants enrolled in a multisite study and had T1w and T2w contrasts. We used the first dataset to develop an automated technique to separate FWML from DAWM and the second and third to validate the automation of the technique. We applied the automatic thresholds to all datasets to assess the overlap of the manual and the automated masks using Dice kappa. We also assessed differences in mean MTR values between NAWM, DAWM and FWML, using manually and automatically derived masks in datasets 1 and 2. Finally, we used the mean intensity of manually-traced areas of NAWM on T2w images as the normalization factor for each MRI contrast, and compared these with the normalized-intensity values obtained using automated NAWM (A-NAWM) masks as the normalization factor. ANOVA assessed the MTR differences across tissue types. Paired t-test or Wilcoxon signed-ranked test assessed FWML and DAWM differences between manual and automatically derived volumes. Pearson correlations assessed the relationship between MTR and normalized intensity values in the manual and automatically derived masks.
Results:
The mean Dice-kappa values for dataset 1 were: 0.79 for DAWM masks and 0.90 for FWML masks. In dataset 2, mean Dice-kappa values were: 0.78 for DAWM and 0.87 for FWML. In dataset 3, mean Dice-kappa values were 0.72 for DAWM, and 0.87 for FWML. Manual and automated DAWM and FWML volumes were not significantly different in all datasets. MTR values were significantly lower in manually and automatically derived FWML compared with DAWM in both datasets (dataset 1 manual: F = 111,08, p < 0.0001; automated: F = 153.90, p < 0.0001; dataset 2 manual: F = 31.25, p < 0.0001; automated: F = 74.04, p < 0.0001). In both datasets, manually derived FWML and DAWM MTR values showed significant correlations with normalized T1w (r = 0.77 to 0.94) intensities.
Conclusions:
The separation of FWML and DAWM on MRI scans of MS patients using automated intensity thresholds on T2w images is feasible. MTR values are significantly lower in FWML than DAWM, and DAWM values are significantly lower than NAWM, reflecting potentially greater demyelination within focal lesions. T1w normalized intensity values exhibit a significant correlation with MTR values in both tissues of interest and could be used as a proxy to assess demyelination when MTR or other myelin-sensitive images are not available.
Insights
Automated MRI analysis can distinguish focal white matter lesions (FWML) from diffusely abnormal white matter (DAWM) in multiple sclerosis (MS). Lower MTR values in FWML indicate greater demyelination, and T1w intensities may serve as a proxy for MTR.
Area of Science:
- Neuroimaging
- Multiple Sclerosis Research
- White Matter Lesion Analysis
Background:
- Histopathology and MRI studies differentiate focal white matter lesions (FWML) from diffusely abnormal white matter (DAWM) in multiple sclerosis (MS).
- These lesion types exhibit distinct histopathological characteristics, including demyelination, axonal loss, and immune cell density.
- These differences may correlate with varying clinical symptoms in MS patients.
Purpose of the Study:
- To develop an automated method for separating FWML and DAWM using T2w MRI intensity thresholds.
- To investigate differences in magnetization transfer ratios (MTR) between FWML and DAWM as a measure of myelin content.
- To correlate MTR values with normalized MRI signal intensities (FLAIR, T2w, T1w) to assess potential surrogates for MTR.
Main Methods:
- Utilized three MRI datasets with varying contrasts (T1w, T2w, FLAIR, MT) from MS participants.
- Developed and validated an automated technique using T2w intensity thresholds to segment FWML and DAWM.
- Assessed segmentation accuracy using Dice kappa and compared MTR values between manually and automatically segmented lesions.
Main Results:
- Automated segmentation of FWML and DAWM showed good agreement with manual segmentation across all datasets (Dice kappa 0.72-0.90).
- Significantly lower MTR values were observed in FWML compared to DAWM, and in DAWM compared to normal appearing white matter (NAWM).
- Significant correlations were found between MTR values and normalized T1w intensities in both FWML and DAWM.
Conclusions:
- Automated separation of FWML and DAWM in MS is feasible using T2w MRI intensity thresholds.
- Lower MTR in FWML suggests greater demyelination, supporting distinct pathological processes.
- Normalized T1w intensity can serve as a potential surrogate for MTR in assessing demyelination when MTR is unavailable.

