ADC measurements in various patterns of multiple sclerosis lesions
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Updated: Aug 9, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Warinthorn Phuttharak1, Waneerat Galassi, Vallop Laopaiboon
1Department of Radiology, Srinagarind Hospital, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand. koiwww@yahoo.com
Objective:
To determine the difference of mean apparent diffusion coefficients (ADC) among different patterns of focal multiple sclerosis (MS) lesions, to compare mean lesion ADC between 2 clinical subgroups and to correlate mean lesion ADC with disability.
Material And Method:
Thirty seven patients (26 with relapsing-remitting multiple sclerosis (MS) and 11 with secondary-progressive MS) underwent both conventional and diffusion-weighted MR imaging of the brain. After creating ADC maps, region identification was done by using b = 0 images and T2-weighted images. ADC values were measured for MS lesions and (NAWM).
Results:
A total of 288 lesions were identified on the images. The mean ADC for the lesions was significantly higher than that of NAWM Hypointense T1 lesions (n = 221) had a significantly higher mean ADC than isointense T1 lesions (n = 67) in both nonenhancing lesions (n = 250) and enhancing lesions (n = 38). The enhanced rim of ring-enhancing lesions (n = 18) had lower ADC than the central nonenhanced portions. Confluent lesions (n = 62) had a substantially higher mean ADC than discrete lesion (n = 226). Mean lesion ADC of secondary progressive MS was significantly higher than relapsing remitting MS. No correlation between mean lesion ADC and (EDSS) score was found
Conclusion:
Quantitative diffusion-weighted imaging is useful to elucidate the heterogeneous pathological substrate of MS in different patterns of MS lesions, to differentiate 2 major clinical subgroups.
Insights
Diffusion-weighted imaging reveals differences in apparent diffusion coefficients (ADC) for multiple sclerosis (MS) lesions. Mean lesion ADC varies by lesion pattern and clinical MS subtype, but not disability.
Area of Science:
- Neuroimaging
- Radiology
- Neurology
Background:
- Multiple sclerosis (MS) is a demyelinating disease characterized by focal lesions in the brain.
- Understanding the heterogeneity of MS lesions is crucial for diagnosis and treatment.
- Diffusion-weighted imaging (DWI) offers quantitative insights into tissue microstructure.
Purpose of the Study:
- To quantify and compare mean apparent diffusion coefficients (ADC) across diverse patterns of focal MS lesions.
- To investigate differences in mean lesion ADC between relapsing-remitting MS (RRMS) and secondary-progressive MS (SPMS) subtypes.
- To explore the correlation between mean lesion ADC and patient disability, assessed by the Expanded Disability Status Scale (EDSS).
Main Methods:
- Conventional and diffusion-weighted MR imaging of the brain was performed on 37 MS patients (26 RRMS, 11 SPMS).
- Apparent diffusion coefficient (ADC) maps were generated, and ADC values were measured for focal MS lesions and normal-appearing white matter (NAWM).
- Lesions were categorized by T1 hypointensity/isointensity, enhancement characteristics, and morphology (confluent vs. discrete).
Main Results:
- A total of 288 MS lesions were analyzed.
- Mean lesion ADC was significantly higher than NAWM ADC.
- Hypointense T1 lesions exhibited higher mean ADC than isointense T1 lesions.
- Confluent lesions showed substantially higher mean ADC than discrete lesions.
- Mean lesion ADC was significantly higher in SPMS patients compared to RRMS patients.
- No significant correlation was found between mean lesion ADC and EDSS scores.
Conclusions:
- Quantitative diffusion-weighted imaging effectively differentiates MS lesions based on their imaging patterns.
- ADC values can help distinguish between different pathological substrates within MS lesions.
- Mean lesion ADC differs between major clinical MS subtypes, suggesting distinct underlying disease processes.
Related Concept Videos
Multiple Sclerosis l: Introduction
Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation

