Brain atrophy and magnetization transfer ratio following methylprednisolone in multiple sclerosis: short-term changes

Robert J Fox1, Elizabeth Fisher, Jean Tkach

  • 1Department of Neurology (Mellen Center), Cleveland Clinic Foundation, Cleveland, OH 44195, USA. foxr@ccf.org

Multiple Sclerosis (Houndmills, Basingstoke, England)
|March 30, 2005
PubMed
Abstract

Insights

Corticosteroid treatment impacts brain parenchymal fraction (BPF) in multiple sclerosis (MS) patients, particularly those with secondary progressive MS (SPMS). This suggests differing therapeutic responses based on MS pathology.

Area of Science:

  • Neuroimaging
  • Neurology
  • Quantitative MRI

Background:

  • Short-term effects of corticosteroids on MRI in multiple sclerosis (MS) are not fully understood.
  • Quantitative MRI measures are crucial for evaluating MS disease activity and treatment efficacy.

Purpose of the Study:

  • To assess the impact of intravenous methylprednisolone (IVMP) on quantitative MRI measures of disease activity and tissue injury in MS patients.
  • To compare changes in MS patients receiving IVMP with a control group not receiving treatment.

Main Methods:

  • Prospective measurement of brain parenchymal fraction (BPF), magnetization transfer ratio (MTR), and lesion volumes over nine weekly MRI scans.
  • Inclusion of ten MS patients receiving IVMP and nine untreated MS patients as controls.

Main Results:

  • BPF declined significantly in IVMP-treated patients compared to controls over eight weeks.
  • BPF decline was more pronounced in secondary progressive MS (SPMS) than in relapsing-remitting MS (RRMS) patients.
  • No significant differences were observed in MTR or lesion volumes between treated and control groups.

Conclusions:

  • SPMS patients exhibit a greater BPF decline post-IVMP compared to RRMS patients.
  • Changes in BPF and MTR suggest altered water content within MS lesions.
  • Differential responses to IVMP in RRMS and SPMS indicate potential fundamental pathological differences influencing therapeutic outcomes.