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Updated: Aug 1, 2025

Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
Published on: February 19, 2021
Unraveling the heterogeneous pathological substrates of relapse-onset multiple sclerosis: a multiparametric
Monica Margoni1,2,3, Elisabetta Pagani1, Paolo Preziosa1,2,4
1Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Background:
In multiple sclerosis (MS), pathological processes affecting brain gray (GM) and white matter (WM) are heterogeneous.
Objective:
To apply a multimodal MRI approach to investigate the regional distribution of the different pathological processes occurring in the brain WM and GM of relapse-onset MS patients.
Methods:
Fifty-seven MS patients (forty-two relapsing remitting [RR], fifteen secondary progressive [SP]) and forty-seven age- and sex-matched healthy controls (HC) underwent a multimodal 3 T MRI acquisition. Between-group voxel-wise differences of brain WM and GM volumes, magnetization transfer ratio (MTR), T1-weighted(w)/T2w ratio, intracellular volume fraction (ICV_f), and quantitative susceptibility mapping (QSM) maps were investigated.
Results:
Compared to HC, RRMS showed significant WM, deep GM and cortical atrophy, significantly lower MTR and T1w/T2w ratio of periventricular and infratentorial WM, deep GM and several cortical areas, lower ICV_f in supratentorial and cerebellar WM and in some cortical areas, and lower QSM values in bilateral periventricular WM (p < 0.001). Compared to RRMS, SPMS patients showed significant deep GM and widespread cortical atrophy, significantly lower MTR of periventricular WM, deep GM and cerebellum, lower T1w/T2w ratio of fronto-temporal WM regions, lower ICV_f of some fronto-tempo-occipital WM and cortical areas. They also had increased QSM and T1w/T2w ratio in the pallidum, bilaterally (p < 0.001).
Conclusion:
A periventricular pattern of demyelination and widespread GM and WM neuro-axonal loss are detectable in RRMS and are more severe in SPMS. Higher T1w/T2w ratio and QSM in the pallidum, possibly reflecting iron accumulation and neurodegeneration, may represent a relevant MRI marker to differentiate SPMS from RRMS.
Insights
Multiple sclerosis (MS) involves heterogeneous brain gray (GM) and white matter (WM) pathology. Multimodal MRI reveals distinct patterns of neurodegeneration in relapsing-remitting MS (RRMS) and secondary progressive MS (SPMS), with pallidal changes potentially differentiating SPMS.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- Multiple sclerosis (MS) exhibits heterogeneous pathological processes affecting both gray matter (GM) and white matter (WM).
- Understanding the regional distribution of these pathologies is crucial for disease characterization.
Purpose of the Study:
- To employ a multimodal magnetic resonance imaging (MRI) approach.
- To investigate the regional distribution of pathological processes in the brain WM and GM of patients with relapse-onset MS.
Main Methods:
- Fifty-seven MS patients (42 relapsing-remitting [RRMS], 15 secondary progressive [SPMS]) and 47 healthy controls (HC) underwent 3T multimodal MRI.
- Voxel-wise differences in WM and GM volumes, magnetization transfer ratio (MTR), T1w/T2w ratio, intracellular volume fraction (ICV_f), and quantitative susceptibility mapping (QSM) were analyzed.
Main Results:
- RRMS patients showed significant WM, deep GM, and cortical atrophy, with reduced MTR, T1w/T2w ratio, and ICV_f in various brain regions compared to HC.
- SPMS patients exhibited more severe deep GM and widespread cortical atrophy, with distinct patterns of reduced MTR, T1w/T2w ratio, and ICV_f compared to RRMS.
- SPMS patients also demonstrated increased pallidal T1w/T2w ratio and QSM, suggesting potential iron accumulation.
Conclusions:
- A periventricular pattern of demyelination and widespread neuro-axonal loss in GM and WM are characteristic of RRMS and are exacerbated in SPMS.
- Elevated T1w/T2w ratio and QSM in the pallidum may serve as a key MRI marker for distinguishing SPMS from RRMS, possibly indicating neurodegeneration and iron deposition.
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