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Diagnostic value of serum and cerebral spinal fluid aquaporin 4-IgG detected by indirect immunofluorescence assays using different base in neuromyelitis optica / 中华神经科杂志
Chinese Journal of Neurology ; (12): 676-679, 2014.
Article en Zh | WPRIM | ID: wpr-469031
Biblioteca responsable: WPRO
ABSTRACT
Objective To explore the diagnostic value of serum and cerebral spinal fluid (CSF) aquaporin 4(AQP4)-IgG detected by indirect immunofluorescence assay (ⅡFA) using monkey optical nerve and AQP4 transfected cell as base in neuromyelitis optica (NMO).Methods Serum and CSF AQP4-IgG in 32 NMO patients,41 multiple sclerosis (MS) patients,33 non-inflammatory neurological disease (NIND) patients and serum AQP4-IgG in 20 healthy controls (HC) were detected by monkey optical nerve/AQP4 transfected cell-based IIFA.Results (1) In both optical nerve and AQP4 transfected cell based IIFA,compared with MS,NIND and HC,the patients with NMO had significantly higher positive rate of AQP4-IgG in both serum (optical nerve-based IIFA:NMO 46.9% (15/32),MS 7.3% (3/41),NIND 3.0% (1/33),HC 0 (0/20),P < 0.01 ; cell-based IIFA:NMO 84.4% (27/32),MS 2.4% (1/41),NIND 3.0% (1/33),HC 0 (0/20),P <0.01) and CSF (optical nerve-based ⅡFA:NMO 21.9% (7/32),MS 0 (0/41),NIND 0 (0/33),P < 0.01 ; cell-based IIFA:NMO 56.3% (18/32),MS 0 (0/41),NIND 0(0/33),P<0.01); sensitivity of serum AQP4-IgG (optical nerve-based IIFA 46.9%; cell-based IIFA 84.4%) was significantly higher than that of CSF AQP4-IgG (optical nerve-based IIFA 21.9%,P <0.01 ; cell-based IIFA 56.3 %,P < 0.05),while no significant difference was found in specificity between serum and CSF AQP4-IgG in diagnosing NMO; using combination of serum and CSF AQP4-IgG applied,the sensitivity increased (optical nerve-based IlFA 46.9% vs 50.0% ; cell-based IIFA 84.4% vs 87.5%) while specificity remained no change.(2) Compared with optical nerve-based IIFA (serum 46.9%,CSF 21.9%),cell-based IIFA had higher sensitivity in diagnosing NMO (serum 84.4% ; CSF 56.3%,P < 0.01),while no significant difference of specificity between these two methods.Conclusion It has better clinical value to detect serum and CSF AQP4-IgG at the same time by AQP4 transfected cell based IIFA in diagnosing NMO.
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Texto completo: 1 Índice: WPRIM Tipo de estudio: Diagnostic_studies Idioma: Zh Revista: Chinese Journal of Neurology Año: 2014 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudio: Diagnostic_studies Idioma: Zh Revista: Chinese Journal of Neurology Año: 2014 Tipo del documento: Article