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Table 2 Seropositivity rates for NMO-IgG and AQP4 autoantibodies in different groups of central nervous system idiopathic inflammatory demyelinating disorders, other neurological disorders, and healthy subjects.

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

Patient/control groups

Number of subjects

Number seropositive for NMO-IgG by tissue-based IIFA (%)

Number seropositive for AQP4 autoantibody by cell-based IIFA (%)

Significance

p value

NMO

18

11 (61%)

14 (78%) [3 +++, 3 ++, 8 +]

ns

Relapsing myelitis

15

6 (40%)

9 (60%) [4 ++, 5 +]

ns

Relapsing myelitis with LETM

12

6 (50%)

9 (75%) [4 ++, 5 +]

ns

Single attack of acute myelitis

25

0

1 (4%) [+]

ns

Single attack of LETM

2

0

1 [+]

ns

Relapsing ON

9

2 (22%)

3 (33%) [2 ++, 1 +]

ns

Single attack of ON

14

1 (7%)

2 (14%) [1 ++, 1 +]

ns

Classical MS

40

0

0

ns

ADEM

7

0

0

ns

Healthy subjects

10

0

0

ns

Other neurological disorders

35

0

0

ns

  1. Abbreviations: NMO = neuromyelitis optica, LETM = longitudinally extensive transverse myelitis, ON = optic neuritis, MS = multiple sclerosis, ADEM = acute disseminated encephalomyelitis, IIFA = indirect immunofluorescence, AQP4 = aquaporin-4, +++ strongly positive, ++ positive, + weakly positive, ns = not significant.