Antibodies against aquaporin-4 in neuromyelitis optica: distinction between recurrent and monophasic patients
Immy A. Ketelslegers, Piet W. Modderman, Anke Vennegoor, Joep Killestein, Dörte Hamann, Rogier Q. Hintzen
Abstract
Immy A. Ketelslegers, Piet W. Modderman, Anke Vennegoor, Joep Killestein, Dörte Hamann, Rogier Q. Hintzen
Abstract
The detection of antibodies against aquaporin-4 (AQP4) has improved the diagnosis of neuromyelitis optica (NMO). We evaluated a recently established cell-based anti-AQP4 assay in 273 patients with inflammatory CNS demyelination. The assay had a specificity of 99% and a sensitivity of 56% to detect all NMO patients and of 74% to detect the recurrent NMO patients, similar to the initial studies reported. AQP4 antibodies were absent in monophasic NMO patients, while samples in recurrent cases remained positive during follow-up. We conclude that the pathogenesis of monophasic NMO may be different from that of relapsing NMO.
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The detection of antibodies against aquaporin-4 (AQP4) has improved the diagnosis of neuromyelitis optica (NMO). We evaluated a recently established cell-based anti-AQP4 assay in 273 patients with inflammatory CNS demyelination. The assay had a specificity of 99% and a sensitivity of 56% to detect all NMO patients and of 74% to detect the recurrent NMO patients, similar to the initial studies reported. AQP4 antibodies were absent in monophasic NMO patients, while samples in recurrent cases remained positive during follow-up. We conclude that the pathogenesis of monophasic NMO may be different from that of relapsing NMO.
Key concepts: Neuromyelitis optica, Aquaporin 4, Medicine, Multiple sclerosis, Antibody, Pathogenesis, Immunology, Pathology