The international cooperative ataxia rating scale in Machado-Joseph disease. Comparison with the unified multiple system atrophy rating scale

Mov Disord. 2007 Oct 15;22(13):1976-9. doi: 10.1002/mds.21735.

Abstract

Our purpose was to evaluate and compare the international cooperative ataxia rating scale (ICARS) and the unified multiple system atrophy rating scale (UMSARS) in patients with Machado-Joseph disease (MJD). We assessed 52 consecutive subjects with MJD using each scale. Both scales had adequate internal consistency (alpha > 0.90), except for the oculomotor (OD) subscore (alpha = 0.08). Patients with dystonia had the highest scores in both scales, and symptoms other than ataxia clearly confounded the total ICARS score. There was a very strong correlation between the ICARS and UMSARS-II (motor function), and the correlations between the ICARS and UMSARS-I (r = 0.79) (history) and UMSARS-IV (r = 0.69) (disability) were also statistically significant. We found no significant changes in scores after a mean interval of 7.7 months, although there was after a mean interval of 13.3 months. We conclude that the total ICARS score is a reliable method for longitudinal evaluation of ataxia in MJD, but a disease specific scale should be developed.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Child
  • Chromosome Aberrations
  • Disability Evaluation
  • Dystonia / diagnosis
  • Dystonia / genetics
  • Female
  • Genes, Dominant
  • Humans
  • Machado-Joseph Disease / diagnosis*
  • Machado-Joseph Disease / genetics
  • Male
  • Middle Aged
  • Multiple System Atrophy / diagnosis*
  • Multiple System Atrophy / genetics
  • Neurologic Examination / methods*
  • Reproducibility of Results
  • Trinucleotide Repeats