Skip to main content
. 2013 Dec 26;2013:614716. doi: 10.1155/2013/614716

Table 1.

Showing the anti-AQP4 antibody, oligoclonal band, and spinal MRI results for patients with idiopathic inflammatory demyelinating disease.

Diagnosis (after incorporating
anti-AQP4 antibody, oligoclonal bands,
and cord lesion length)
Anti-AQP4 antibody Cerebrospinal fluid
for oligoclonal bands
Spine MRI
Positive Negative Positive Negative Cord lesion
length ≤ 3 VS
Cord lesion
length > 3 VS
Clinical Diagnosis
 MS
  CIS (MRI brain CDMS) 0 7 5 2 5 (in two no lesions) 0
  CDMS 0 91 30 16 55 22
  Opticospinal recurrent type of
  multiple sclerosis
8** 2 0 10 4 6*
  Spinal multiple sclerosis 1# 4 3 2 5 0
 NMO 31 4 1 43 2 33
 NMOSD
  Single episode optic neuritis/relapsing
  optic neuritis
3 1 0 0 0 0
  Single episode transverse
  myelitis/relapsing transverse myelitis
7 2 0 9 1 8
  Brain lesions typical of NMOSD 6 3 1 8 4 5

 Other IIDDs
  ADEM 0 26 1 25 8 18
  Single episode optic neuritis
  (undeclared as NMO or MS, no
  brain/cord lesions)
0 7 0 7 0 0
  Single episode transverse myelitis
  undeclared as NMO/MS
0 20 0 10 8 12
  Unclassified single episode
  demyelinating disease of the brain
  (undifferentiated from
  NMOSD/ADEM/MS/non-IDDS)
0 8 0 8 0 0
  Unclassified relapsing optic neuritis
  (MRI of brain and spine negative for
   MS or NMO/NMOSD)
0 3 0 3 0 0

MS: multiple sclerosis; NMO: neuromyelitis optica; NMOSD: neuromyelitis optica spectrum disorder; VS: vertebral segments.

*Six patients initially diagnosed with opticospinal variants of Multiple sclerosis upon reviewing first MRI at onset of disease were found to have longitudinally extensive cord lesions.

**Eight patients reclassified as NMO.

#Reclassified as NMOSD.