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Incidence of AQP4-IgG seropositive neuromyelitis optica spectrum disorders in the Netherlands: About one in a million.
Daniëlle van Pelt, E; Wong, Yu Yi M; Ketelslegers, Immy A; Siepman, Dorine Am; Hamann, Dörte; Hintzen, Rogier Q.
Afiliação
  • Daniëlle van Pelt E; Department of Neurology, MS Centre Erasmus, the Netherlands.
  • Wong YYM; Department of Neurology, MS Centre Erasmus, the Netherlands.
  • Ketelslegers IA; Department of Neurology, MS Centre Erasmus, the Netherlands.
  • Siepman DA; Department of Neurology, MS Centre Erasmus, the Netherlands.
  • Hamann D; Department of Immunopathology and Blood Coagulation, Sanquin Diagnostic Services, the Netherlands.
  • Hintzen RQ; Department of Neurology, MS Centre Erasmus, the Netherlands.
Mult Scler J Exp Transl Clin ; 2: 2055217315625652, 2016.
Article em En | MEDLINE | ID: mdl-28607712
ABSTRACT
Neuromyelitis optica (NMO) is a rare autoimmune disease affecting the optic nerves and spinal cord. In the majority of NMO patients anti-aquaporin-4 antibodies (AQP4-IgG) are detected. Here we assessed a nationwide incidence of AQP4-IgG-seropositive NMO spectrum disorders (NMOSD) in the Netherlands based on results of one central laboratory. Data were collected since the introduction of the highly sensitive cell-based assay for six consecutive years. Samples from 2795 individual patients have been received; of them 94 (3.4%) were seropositive. Based on the Dutch population with 16.6 million inhabitants, the mean incidence of AQP4-IgG-seropositive NMOSD was calculated at 0.09 per 100,000 people.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Incidence_studies / Risk_factors_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Incidence_studies / Risk_factors_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article