4.3 Article

Anti-aquaporin-4 antibody in Chinese patients with central nervous system inflammatory demyelinating disorders

Journal

CLINICAL NEUROLOGY AND NEUROSURGERY
Volume 114, Issue 8, Pages 1131-1134

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.clineuro.2012.01.022

Keywords

Neuromyelitis optica; Multiple sclerosis; Aquaporin; NMO-IgG; Diagnosis; Central nervous system

Funding

  1. Technology Project of Guangzhou City [2060402]

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Objective: To determine seroprevalence of aquaporin-4 (AQP4) antibody in Chinese patients with central nervous system (CNS) inflammatory demyelinating disorders. Methods: AQP4 antibody was detected by anti-AQP4 antibody assay. We measured seroprevalence in 200 patients with neuromyelitis optica (NMO, n = 44), multiple sclerosis (MS, n = 46), transverse myelitis (TM, n = 44), optic neuritis (ON, n = 13), acute disseminated encephalomyelitis (ADEM, n = 2), and other neurological diseases (OND, n = 51). Results: AQP4 antibody seropositivity was 88.6% in patients with NMO, 4.3% in patients with MS, 30.8% in patients with ON and 51.7% in patients with LETM (longitudinally extensive TM). No patients with acute partial TM, ADEM, OND were positive for AQP4 antibody. Sensitivity of the test was 88.6% (95% CI 80-95) in patients with NMO. Specificity is 97.9% (95% Cl 95.1-100) in 46 MS patients, with 51 OND patients as the control group. If the patients with recurrent ON. LETM were considered high risk for NMO (n = 37) and the remaining patients (n = 119) were considered controls, the sensitivity of this assay would be 48.6% (95% CI 33.4-64.1) and the specificity 97.5% (95% Cl 94.7-100). Conclusion: This study confirms that AQP4 antibody is a sensitive and specific biomarker for discrimination between NMO and other CNS autoimmune diseases. (C) 2012 Published by Elsevier B.V.

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