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Demographic and clinical features of neuromyelitis optica: A review.

  • Author(s): Pandit, L;
  • Asgari, N;
  • Apiwattanakul, M;
  • Palace, J;
  • Paul, F;
  • Leite, MI;
  • Kleiter, I;
  • Chitnis, T;
  • GJCF International Clinical Consortium & Biorepository for Neuromyelitis Optica
  • et al.
Abstract

The comparative clinical and demographic features of neuromyelitis optica (NMO) are not well known. In this review we analyzed peer-reviewed publications for incidence and prevalence, clinical phenotypes, and demographic features of NMO. Population-based studies from Europe, South East and Southern Asia, the Caribbean, and Cuba suggest that the incidence and prevalence of NMO ranges from 0.05-0.4 and 0.52-4.4 per 100,000, respectively. Mean age at onset (32.6-45.7) and median time to first relapse (8-12 months) was similar. Most studies reported an excess of disease in women and a relapsing course, particularly in anti-aquaporin 4 antibody (anti AQP4-IgG)-positive patients. Ethnicity may have a bearing on disease phenotype and clinical outcome. Despite limitations inherent to the review process, themes noted in clinical and demographic features of NMO among different populations promote a more global understanding of NMO and strategies to address it.

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