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Table 2 Demographic and clinical characteristics of NMOSD with and without CTD

From: Neuromyelitis optica spectrum disorders with and without connective tissue disorders

 

NMOSD (39)

NMOSD with CTD (18)

P

Gender, n (% female)

37 (94.9%)

18 (100%)

0.839

Age at onset, years

39.97 ± 13.82

42.33 ± 11.29

0.530

Follow-up duration, years

5.63 ± 4.63

5.04 ± 3.83

0.641

Annualized relapse rate (ARR)

0.98 ± 0.54

1.40 ± 1.51

0.127

ARR before regular medication

1.58 ± 2.18

1.66 ± 1.44

0.899

ARR after regular medication

0.64 ± 0.79

1.39 ± 1.96

0.100

Number of attacks

3.97 ± 2.07

4.28 ± 2.32

0.623

Neuropathic pain, n (%)

21 (53.8%)

10 (55.6%)

0.904

EDSS at nadir

3.5 (1, 8)

4 (1.5, 8.5)

0.031*

 Visual functions

0 (0, 6)

1 (0, 6)

0.139

 Pyramidal functions

1 (0, 4)

2 (0, 4)

0.219

 Sensory functions

2 (0, 4)

3 (0, 4)

0.007*

 Bowel and bladder

0 (0, 5)

3 (0, 5)

0.256

EDSS at last follow-up

2 (1, 8)

2.5 (1.5, 8.5)

0.403

 Visual functions

0 (0, 4)

1 (0, 6)

0.111

 Pyramidal functions

1 (0, 4)

1 (0, 4)

0.595

 Sensory functions

1 (0, 4)

2 (0, 4)

0.063

 Bowel and bladder

0 (0, 5)

0 (0, 5)

0.856

Initial presentation, n (%)

 ON

14 (35.9%)

6 (33.3%)

0.850

 Area postrema syndrome

8 (20.5%)

2 (11.1%)

0.622

 AM

15 (38.5%)

9 (50.0%)

0.412

 Others

2 (5.1%)

1 (5.6%)

1.000

  1. Abbreviations: NMOSD neuromyelitis optica spectrum disorders, CTD connective tissue disorders, EDSS Kurtzke Expanded Disability Status Scale, ON optica neuritis, AM acute myelitis
  2. *P < 0.05