Table 2

Comparison between seropositive and seronegative neuromyelitis optica

Seropositive neuromyelitis opticaSeronegative neuromyelitis opticap Value
No of patients38219
Male:female (female%)32:344 (91.5%)5:14 (73.6%)0.0241*
Age at onset (median, year)45 (6–86)33 (15–70)0.0179
Disease duration (median, year)5 (1–46)8 (1–36)0.3433
Annual relapse rate (median)1.0 (0.1–9.0)1.4 (0.2–4.0)0.8860
Extended Disability Status Scale score (median)6.5 (0–10)7.5 (4–9)0.1511
Visual outcome
 Blindness61/350 (17.4%)4/19 (21.0%)NS
 Severe impairment114/350 (32.5%)15/19 (78.9%)0.00010
First attack
 Optic nerve162/382 (42.4%)11/19 (57.8%)NS
 Spinal cord203/382 (53.1%)6/19 (31.5%)NS
 Brainstem29/382 (7.5%)0/19 (0.0%)NS
 Cerebrum30/382 (7.8%)3/19 (15.7%)NS
MRI lesions
 Spinal cord342/372 (91.9%)19/19 (100%)NS
 Longitudinally extensive transverse myelitis326/372 (87.6%)19/19 (100%)NS
 Cerebrum196/365 (53.6%)13/19 (68.4%)NS
 Optic nerve129/369 (34.9%)13/19 (68.4%)0.0031
 Brainstem103/364 (28.2%)8/19 (42.1%)NS
Systemic disease
 Sjögren syndrome34/168 (20.2%)1/8 (12.5%)NS
 Thyroid diseases20/169 (11.8%)2/8 (25.0%)NS
Autoantibody
 Sjögren syndrome A antibody or Sjögren syndrome B antibody64/188 (34.0%)1/9 (11.1%)NS
 Antinuclear autoantibody99/188 (52.6%)1/9 (11.1%)0.036
Cerebrospinal fluid
 Oligoclonal band22/221 (9.9%)2/15 (13.3%)NS
 Myelin basic protein121/207 (58.4%)6/12 (50.0%)NS
  • * Statistically significant by the Fisher exact probability test.

  • Statistically significant by Mann–Whitney U test.

  • Statistically significant by χ2 test.