Characterizing mortality in patients with AQP4-Ab+ neuromyelitis optica spectrum disorder

Ann Clin Transl Neurol. 2024 Jul;11(7):1942-1947. doi: 10.1002/acn3.52092. Epub 2024 Jun 17.

Abstract

Neuromyelitis optica spectrum disorder is an autoimmune disease, causing severe disability due to relapses, but recent mortality data are limited. Among 396 patients seropositive for anti-aquaporin-4 antibody from 2014 to 2020 in the United Kingdom, 39 deaths occurred: 19 (48.7%) were unrelated to disease; 14 (35.9%) were severe disability- or relapse-related; and 4 (10.3%) were attributed to malignancy/infection. Mean annual mortality was 1.92% versus 0.63% in the matched population. The standardized mortality ratio was 3.04 (95% confidence interval 1.67-5.30) with 1.29% excess mortality per year in patients. Median Expanded Disability Status Scale before death was 7.0. Results highlight the importance of preventing relapses that drive disability.

MeSH terms

  • Adult
  • Aged
  • Aquaporin 4* / immunology
  • Autoantibodies* / blood
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neuromyelitis Optica* / blood
  • Neuromyelitis Optica* / immunology
  • Neuromyelitis Optica* / mortality
  • United Kingdom / epidemiology
  • Young Adult

Substances

  • Aquaporin 4
  • AQP4 protein, human
  • Autoantibodies

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