Annals of Clinical and Translational Neurology (Jul 2024)

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

  • Anna Francis,
  • Emily Gibbons,
  • Jeffrey Yu,
  • Karissa Johnston,
  • Hannah Rochon,
  • Lauren Powell,
  • Maria Isabel Leite,
  • Saif Huda,
  • Adrian Kielhorn,
  • Jacqueline Palace

DOI
https://doi.org/10.1002/acn3.52092
Journal volume & issue
Vol. 11, no. 7
pp. 1942 – 1947

Abstract

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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.