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.
| Original language | English |
|---|---|
| Pages (from-to) | 2055217315625652 |
| Journal | Multiple sclerosis journal - experimental, translational and clinical |
| Volume | 2 |
| DOIs | |
| Publication status | Published - 26 Jan 2016 |
| Externally published | Yes |
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