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Table 3 Clinical and neuroradiological characteristics of 23 patients with neuromyelitis optica or relapsing myelitis who are seropositive for AQP4 autoantibodies by cell-based IIFA, divided into those who are seropositive and seronegative for NMO-IgG by tissue-based IIFA.

From: Aquaporin-4 autoantibodies in neuromyelitis optica spectrum disorders: comparison between tissue-based and cell-based indirect immunofluorescence assays

 

NMO IgG +ve (n = 17)

NMO-IgG -ve (n = 6)

Significance p value

Female (%)

15 (88%)

6 (100%)

ns

Mean onset age in years (range)

42.0 (18-64)

52.8 (17-70)

ns

Mean duration of follow-up in years (range)

6.6 (2-15)

3.9 (2-8)

ns

Patients with LETM (%)

16 (94%)

6 (100%)

ns

Mean myelitis attack rate in no. of attacks per year (range)

0.8 (0.2-2.0)

0.7 (0.3-1.0)

ns

Mean myelitis attack rate in first 2 years of disease in no. of attacks per year

1.6 (0.5-3.0)

1.4 (0.5-4.0)

ns

Mean length of MRI T2W hyperintense signal abnormalities in no. of vertebral segments (range)

5.3 (2-17)

5.7 (3-10)

ns

Patients with MRI brain lesions compatible with inflammatory demyelination (%)

10 (59%)

3 (50%)

ns

Patients with CSF OCB (%)

2 (12%)

0

ns

Patients with other autoimmune disorders or autoantibodies (%)

5 (29%)

1 (17%)

ns

Patients with poor visual outcome (%)

4 (24%)

1 (17%)

ns

Mean EDSS score at latest follow-up (range)

5.9 (2.0-10)

6.8 (6.0-8.0)

ns

Patients with poor neurological outcome (%)

11 (65%)

6 (100%)

ns

  1. Abbreviations: NMO = neuromyelitis optica, AM = acute myelitis, LETM = longitudinally extensive transverse myelitis, MRI = magnetic resonance imaging, CSF = cerebrospinal fluid, OCB = oligoclonal bands, EDSS = Expanded Disability Status Scale, ns = not significant.