Weekly follow up of acute lesions in three early multiple sclerosis patients using MR spectroscopy and diffusion

Gabriel Kocevar1, Claudio Stamile1, Salem Hannoun2

  • 1CREATIS, UMR5520, U1206 Inserm, université Claude-Bernard-Lyon1, 69621 Lyon, France.

Abstract

Insights

Multimodal magnetic resonance imaging reveals inflammation and demyelination in multiple sclerosis (MS) lesions. Diffusion tensor imaging and MR spectroscopy track disease progression and potential remyelination, aiding in understanding MS pathophysiology.

Area of Science:

  • Neuroimaging
  • Neurology
  • Biomedical Engineering

Background:

  • Multiple sclerosis (MS) lesion formation involves complex pathophysiological processes including inflammation, demyelination, remyelination, and axonal damage.
  • The precise temporal evolution of these processes in MS lesions remains incompletely understood.
  • Multimodal magnetic resonance (MR) techniques offer potential for detailed monitoring of these dynamic changes.

Purpose of the Study:

  • To investigate the temporal evolution of pathophysiological mechanisms in acute white matter lesions in multiple sclerosis (MS).
  • To assess the utility of a weekly multimodal MR protocol, including conventional MRI, diffusion tensor imaging (DTI), and localized MR spectroscopy (MRS), in characterizing MS lesions.
  • To explore the relationship between blood-brain barrier (BBB) disruption, inflammation, and demyelination using advanced MR techniques.

Main Methods:

  • Three untreated patients with early relapsing-remitting MS and one healthy control were monitored weekly for two months.
  • A multimodal MR protocol comprising conventional MRI, DTI, and MRS was applied to the largest gadolinium-enhancing lesion.
  • Diffusion metrics (mean diffusivity, fractional anisotropy) and metabolite ratios (Cho/Cr, mI/Cr) were analyzed over time.

Main Results:

  • Diffusion metrics indicated increased mean diffusivity and decreased fractional anisotropy in MS lesions compared to controls.
  • Elevated Cho/Cr ratios persisted in lesions throughout the follow-up period.
  • Temporal profiles of mI/Cr ratios varied, with delayed increases observed in two patients, suggesting different post-lesion formation pathological processes. Blood-brain barrier recovery was noted after three weeks.

Conclusions:

  • Multimodal MR imaging, combining DTI and MRS, effectively elucidates temporal relationships between BBB disruption, inflammation, and demyelination in MS.
  • Diffusion metrics demonstrate high sensitivity for detecting inflammatory processes in MS lesions.
  • Distinct temporal patterns of mI/Cr ratios may offer specificity in monitoring post-lesion formation mechanisms like glial proliferation and remyelination.

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