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Updated: Aug 17, 2026

Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
Published on: February 19, 2021
Dynamic susceptibility contrast perfusion MR imaging of multiple sclerosis lesions: characterizing hemodynamic
Yulin Ge1, Meng Law, Glyn Johnson
1Department of Radiology, New York University School of Medicine, NY 10016, USA.
Background And Purpose:
Perfusion measurement in multiple sclerosis (MS) may cast light on the disease pathogenesis and lesion development since vascular pathology is frequently demonstrated in the disease. This study was performed to investigate the perfusion characteristics in MS lesions using dynamic susceptibility contrast MR imaging (DSC-MRI) to better understand the hemodynamic changes in MS.
Methods:
Seventeen patients with relapsing-remitting MS were studied with DSC-MRI. Perfusion measurements included cerebral blood flow (CBF), cerebral blood volume (CBV), and mean transit time (MTT), were obtained in enhancing, non-enhancing lesions covered by DSC-MRI and contralateral normal appearing white matter (NAWM) in patients as well as normal white matter in seventeen control subjects.
Results:
DSC-MRI data demonstrated reduced perfusion with significantly prolonged MTT (P < 0.001) in lesions and NAWM in patients compared with normal white matter in controls. Compared to contralateral NAWM, enhancing lesions demonstrate increased CBF (P = 0.007) and CBV (P < 0.0001), indicating inflammation-mediated vasodilatation. A K means cluster analysis was performed and identifies approximately 63.8% of non-enhancing lesions (Class 1) with significantly decreased perfusion (P < or = 0.0001) when compared with contralateral NAWM. In contrast, the remainder 36.2% non-enhancing lesions (Class 2) show increased CBV (P = 0.02) in a similar fashion to enhancing lesions and can be observed on quantitative color-coded maps even without blood-brain barrier breakdown.
Conclusion:
DSC-MRI measurements demonstrate potential for investigating hemodynamic abnormalities that are associated with inflammatory activity, lesion reactivity and vascular compromise in MS lesions. Non-enhancing lesions showed both low and high perfusion suggesting microvascular abnormalities with hemodynamic impairment and inflammatory reactivity that cannot be seen on conventional MRI.
Insights
Dynamic susceptibility contrast MRI reveals altered perfusion in multiple sclerosis (MS) lesions and normal-appearing white matter. These hemodynamic changes, including prolonged mean transit time, offer insights into MS pathogenesis and lesion development.
Area of Science:
- Neurology
- Radiology
- Medical Imaging
Background:
- Vascular pathology is frequently observed in multiple sclerosis (MS).
- Perfusion measurement may elucidate MS pathogenesis and lesion development.
- Hemodynamic changes are critical to understanding MS progression.
Purpose of the Study:
- Investigate perfusion characteristics in MS lesions using dynamic susceptibility contrast MR imaging (DSC-MRI).
- Understand hemodynamic changes in MS.
- Correlate perfusion abnormalities with disease activity and lesion type.
Main Methods:
- Seventeen patients with relapsing-remitting MS underwent DSC-MRI.
- Perfusion parameters measured: cerebral blood flow (CBF), cerebral blood volume (CBV), and mean transit time (MTT).
- Measurements were taken in enhancing lesions, non-enhancing lesions, normal-appearing white matter (NAWM), and control white matter.
Main Results:
- MS lesions and NAWM showed significantly prolonged MTT compared to controls.
- Enhancing lesions exhibited increased CBF and CBV, suggesting inflammation-driven vasodilation.
- Non-enhancing lesions were heterogeneous: 63.8% showed decreased perfusion, while 36.2% displayed increased CBV.
Conclusions:
- DSC-MRI can identify hemodynamic abnormalities in MS lesions related to inflammation and vascular compromise.
- Perfusion patterns in non-enhancing lesions suggest microvascular abnormalities and inflammatory reactivity not visible on conventional MRI.
- DSC-MRI provides valuable insights into the complex pathophysiology of MS lesions.
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