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Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
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Diffusion tensor imaging in multiple sclerosis at different final outcomes.

O Andersen1, A Hildeman2, M Longfils2

  • 1Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Acta Neurologica Scandinavica
|July 26, 2017
PubMed
Summary
This summary is machine-generated.

Diffusion tensor imaging (DTI) reveals that increased radial diffusivity (RD) in the corpus callosum indicates myelin loss, distinguishing secondary progressive multiple sclerosis (MS) from benign MS courses.

Keywords:
axial diffusivitydiffusion tensor imagingfractional anisometropymagnetic resonance imagingmultiple sclerosisradial diffusivityrelapsing-remitting phasesecondary progressive phase

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Area of Science:

  • Neuroimaging
  • Neurology
  • Biomedical Engineering

Background:

  • Multiple Sclerosis (MS) presents diverse long-term outcomes, necessitating methods to differentiate demyelination from axonal degeneration.
  • Evaluating the relative contributions of these pathological processes is crucial for understanding MS progression.

Purpose of the Study:

  • To employ diffusion tensor imaging (DTI) to assess demyelination and axonal degeneration in the corpus callosum (CC) of MS patients.
  • To correlate DTI metrics with different long-term MS disease courses.

Main Methods:

  • DTI measures, including mean diffusivity (MD), fractional anisotropy (FA), axial diffusivity (AD), and radial diffusivity (RD), were analyzed in the CC of 31 MS patients.
  • Patients were categorized by disease course: secondary progressive (n=13), non-progressive (n=11), and monophasic (n=7).
  • A cohort of 254 attack-onset MS patients with 50-year follow-up and five healthy controls were included.

Main Results:

  • Secondary progressive MS patients showed increased RD and reduced FA in the CC compared to other groups.
  • No significant differences in DTI parameters were found between non-progressive, monophasic MS groups, and controls.
  • Axial diffusivity (AD) did not differ across the groups, suggesting it's not a key indicator of long-term outcome.

Conclusions:

  • Elevated RD in the corpus callosum is indicative of significant myelin loss, characterizing secondary progressive MS.
  • Normal RD values in clinically isolated syndrome and non-progressive MS groups confirm their generally benign nature.
  • Demyelination, identified by increased RD, serves as a distinguishing feature for secondary progressive MS, differentiating it from less aggressive forms.