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Spinal cord atrophy in multiple sclerosis and relationship with disability across clinical phenotypes

Published:November 17, 2014DOI:https://doi.org/10.1016/j.msard.2014.11.002

      Highlights

      • Spinal cord atrophy in multiple sclerosis in the upper cervical cord can be measured in a reliable and reproducible manner.
      • Spinal cord has a robust correlation with clinical disability as measured by EDSS in both relapsing and progressive MS.
      • Patients with progressive forms of MS have greater loss of spinal cord volume than relapsing-remitting MS.
      • In multivariate analysis, disease duration and upper cervical cord volume were independent predictors of disability, where as gender and age were not.

      Abstract

      Background

      Several studies have shown a relationship between spinal cord atrophy and clinical disability in patients with multiple sclerosis (MS).

      Objectives

      We examined the correlation between cervical cord cross-sectional area at the C2 vertebral level (CSA-C2) and the expanded disability status scale (EDSS) in patients with relapsing-remitting and progressive forms of MS. The latter included both secondary and primary progressive MS patients.

      Methods

      A total of 150 patients with MS were recruited from the Wayne State University MS clinic. Ninety-three had relapsing-remitting MS and 57 patients had progressive MS. MRI scan of the cervical cord was obtained for each patient. Correlation studies and multivariate regression analysis was performed, blinded to clinical status.

      Results

      The mean age was 41.3 year old, 64.6% were women, mean disease duration was 11.2 years, CSA-C2 was 80.2 mm2 and mean EDSS was 3.8. There was significant correlation between CSA-C2 and EDSS (r −0.75, p<0.0001). Sub-group analysis showed CSA-C2 was 68.6 mm2 and 87.3 mm2 in the progressive and relapsing-remitting groups, respectively (p<0.0001). Multivariable regression showed that CSA-C2 was a significant predictor of disability independent of disease duration, and phenotype.

      Conclusions

      Our study demonstrates that CSA-C2 has a strong correlation with clinical disability in both RRMS and progressive MS. Greater spinal cord atrophy was seen in patients with progressive than relapsing-remitting MS. CSA-C2, disease duration, and phenotype are independent predictors of disability.

      Keywords

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