alexion test
Disease progression
The interval between attacks can vary widely, lasting months or even years; however, the relapsing course may lead to functional impairments, with more than a fifth of patients requiring gait assistance within five years.1,4

* A retrospective study of Mayo Clinic records including 163 patients with NMO; 110 (67%) were seropositive and 53 (33%) were scored seronegative.4

Based on a study comparing the clinical outcomes and long-term prognostic characteristics of 106 aquaporin-4 antibody-seropositive patients from the UK and Japan.5

Relapse is defined as the onset of new or worsening of original symptoms, with a duration of more than 24 hours, in the absence of other recognised causes such as fever and infection.*7

The effects of NMOSD relapses include vision loss, pain and paralysis.4,5 Almost half of patients with NMOSD can experience one or more relapses, resulting in hospital/inpatient admissions and ambulatory/outpatient treatments within 2 years.8

Following an NMOSD attack, many patients do not fully recover and there is an increased risk of essential function loss with subsequent attacks.2

76% of patients experience only partial or no recovery from myelitis after the first attack.†2

* Some studies further defined relapse as an increase of at least 0.5 on the extended disability status scale (EDSS), an increase of at least 1 on two functional system (FS) scales, or an increase of at least 2 on one FS scale.7

(n = 93/123).2
* A retrospective study of 175 patients of whom 156 (89.1%) were relapsing and 137 (78.3%) were AQP4 positive.2
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AQP4, aquaporin-4; EDSS, extended disability status scale; NMOSD, neuromyelitis optica spectrum disorder.
Wingerchuk DM, Lucchinetti CF. Neuromyelitis optica spectrum disorder. N Engl J Med. 2022;387(7):631–639. Jarius S, et al. Contrasting disease patterns in seropositive and seronegative neuromyelitis optica: A multicentre study of 175 patients. J Neuroinflammation. 2012;9(1):14. Huda S, et al. Neuromyelitis optica spectrum disorders. Clin Med. 2019;19(2):169–176. Jiao Y, et al. Updated estimate of AQP4-IgG serostatus and disability outcome in neuromyelitis optica. Neurology. 2013;81(14):1197–1204. Kitley J, et al. Prognostic factors and disease course in aquaporin-4 antibody-positive patients with neuromyelitis optica spectrum disorder from the United Kingdom and Japan. Brain. 2012;135(pt 6):1834–1849. Mandler RN. Neuromyelitis optica – Delvic’s syndrome, update. Autoimmun Rev. 2006;5(8):537–543. Ma X, et al. Risk of relapse in patients with neuromyelitis optica spectrum disorder: Recognition and preventative strategy. Mult Scler Relat Disord. 2020;46:102522. Royston M, et al. Neuromyelitis optica spectrum disorder: Clinical burden and cost of relapses and disease-related care in US clincial practice. Neurol Ther. 2021;10(2):767–783.
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