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Published on: June 30, 2014
Brain Iron at Quantitative MRI Is Associated with Disability in Multiple Sclerosis
Robert Zivadinov1, Eleonora Tavazzi1, Niels Bergsland1
1From the Buffalo Neuroimaging Analysis Center, Department of Neurology, Jacobs School of Medicine and Biomedical Sciences (R.Z., E.T., N.B., J.H., F.L., M.G.D., E.C., D.R., J.D., F.S.), Center for Biomedical Imaging, Clinical Translational Science Institute (R.Z.), and Jacobs Multiple Sclerosis Center, Department of Neurology, School of Medicine and Biomedical Sciences (C.K., D.H., B.W.G.), University at Buffalo, State University of New York, 100 High St, Buffalo, NY 14203.
Quantitative susceptibility mapping (QSM) reveals deep gray matter iron changes in multiple sclerosis (MS) are linked to disease progression and disability, independent of atrophy.
Area of Science:
- Neuroimaging
- Neurodegeneration
- Magnetic Resonance Imaging
Background:
- Multiple sclerosis (MS) involves complex neurodegenerative processes affecting deep gray matter.
- Assessing iron deposition in deep gray matter is crucial for understanding MS evolution and disability.
- Quantitative susceptibility mapping (QSM) offers a novel method to measure iron-related changes.
Purpose of the Study:
- To investigate deep gray matter susceptibility in MS using QSM.
- To evaluate the association between deep gray matter susceptibility and clinical disability in MS patients.
- To compare susceptibility differences between MS patients and healthy controls.
Main Methods:
- Prospective study of 600 MS patients and 250 healthy controls using 3.0-T MRI.
- Quantitative susceptibility mapping (QSM) to measure magnetic susceptibility in deep gray matter.
- Region of interest and voxelwise analyses, controlling for age and sex, to assess associations with clinical outcomes.
Main Results:
- MS patients showed lower thalamic susceptibility and higher basal ganglia susceptibility compared to controls.
- Lower thalamic susceptibility correlated with longer disease duration, greater disability, and progressive MS.
- Higher globus pallidus susceptibility was associated with increased disability, independent of atrophy.
Conclusions:
- Altered deep gray matter iron, detected by QSM, is associated with MS progression and disability.
- These findings suggest iron deposition plays a role in MS pathogenesis and clinical outcomes.
- QSM provides valuable insights into MS pathophysiology beyond tissue atrophy.
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