Disability in progressive MS is associated with T2 lesion changes

C Ammitzbøll, T B Dyrby, M Lyksborg, K Schreiber, R Ratzer, J Romme Christensen, P Iversen, M Magyari, E Garde, P S Sørensen, H R Siebner, F Sellebjerg

2 Citations (Scopus)

Abstract

BACKGROUND: Progressive multiple sclerosis (MS) is characterised by diffuse changes on brain magnetic resonance imaging (MRI), which complicates the use of MRI as a diagnostic and prognostic marker. The relationship between MRI measures (conventional and non-conventional) and clinical disability in progressive MS therefore warrants further investigation.

OBJECTIVE: To investigate the relationship between clinical disability and MRI measures in patients with progressive MS.

METHODS: Data from 93 primary and secondary progressive MS patients who had participated in 3 phase 2 clinical trials were included in this cross-sectional study. From 3T MRI baseline scans we calculated total T2 lesion volume and analysed magnetisation transfer ratio (MTR) and the diffusion tensor imaging indices fractional anisotropy (FA) and mean diffusivity (MD) in T2 lesions, normal-appearing white matter (NAWM) and cortical grey matter. Disability was assessed by the Expanded Disability Status Scale (EDSS) and the MS functional composite.

RESULTS: T2 lesion volume was associated with impairment by all clinical measures. MD and MTR in T2 lesions were significantly related to disability, and lower FA values correlated with worse hand function in NAWM. In multivariable analyses, increasing clinical disability was independently correlated with increasing T2 lesion volumes and MTR in T2 lesions.

CONCLUSION: In progressive MS, clinical disability is related to lesion volume and microstructure.

Original languageEnglish
JournalMultiple Sclerosis and Related Disorders
Volume20
Pages (from-to)73-77
ISSN2211-0348
DOIs
Publication statusPublished - Feb 2018

Keywords

  • Brain/diagnostic imaging
  • Cohort Studies
  • Cross-Sectional Studies
  • Diffusion Tensor Imaging
  • Disability Evaluation
  • Female
  • Gray Matter/diagnostic imaging
  • Humans
  • Male
  • Middle Aged
  • Multiple Sclerosis, Chronic Progressive/diagnostic imaging
  • White Matter/diagnostic imaging

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