Table 1 Baseline characteristics of patients with NMOSD and MS.

From: Distinct prognostic implications of blood neuronal and astroglial biomarkers in neuromyelitis optica spectrum disorders versus multiple sclerosis

Ā 

NMOSD

MS

p

p’

Ā 

(n = 41)

(n = 92)

Age, median [IQR]

50.0 [45.5–60.5]

44.0 [35.0–53.8]

< 0.001

Ā 

Age at onset, median [IQR]

43.0 [33.5–52.0]

32.0 [23.0–39.8]

< 0.001

Ā 

Female, n (%)

37 (90.2)

65 (70.7)

0.014

Ā 

Education, median [IQR]

12.0 [12.0–16.0]

16.0 [12.0–16.0]

0.049

Ā 

Disease duration, years, median [IQR]

9.0 [4.5–13.0]

11.0 [7.3–14.0]

0.030

Ā 

Last Clinical Attack location, n (%)

Ā Ā 

0.076

Ā 

ON

8 (19.5)

16 (17.4)

Ā Ā 

TM

26 (63.4)

36 (39.1)

Ā Ā 

Brain

5 (12.2)

31 (33.7)

Ā Ā 

ON + TM

0

2 (2.2)

Ā Ā 

ON + Brain

1 (2.4)

2 (2.2)

Ā Ā 

TM + Brain

1 (2.4)

5 (5.4)

Ā Ā 

EDSS, median [IQR]

2.5 [2.0–4.0]

2.0 [1.0–3.5]

0.041

0.912

PST score, median [IQR]

41.0 [19.0–53.5]

47.0 [36.3–63.0]

0.019

0.723

Immune modulatory agenta, n (%)

40 (97.6)

85 (92.4)

0.247

Ā 

B-cell depleting treatment (BCDT)

12 (29.3)

Ā Ā Ā 

Non-B-cell depleting treatment

28 (68.3)

Ā Ā Ā 

High-efficacy treatment

Ā 

20 (21.7)

Ā Ā 

Low-efficacy treatment

Ā 

65 (70.7)

Ā Ā 

Blood biomarker

Ā Ā Ā Ā 

sGFAP, pg/mL, median [IQR]

127.2 [102.6–229.3]

90.0 [68.1–129.0]

< 0.001

0.036

sNfL, pg/mL, median [IQR]

12.9 [9.1–20.3]

9.8 [7.6–14.7]

0.033

0.929

  1. EDSS = Expanded disability status scale; MS = Multiple sclerosis; NMOSD = Neuromyelitis optica spectrum disorder; ON = Optic neuritis; PST = Processing speed test; sGFAP = Serum glial fibrillary acidic protein; sNfL = Serum neurofilament light chain; TM = Transverse myelitis.
  2. aNMOSD patients were treated with Azathioprine (n = 19), Rituximab (n = 12), Mycophenolate mofetil (n = 9). MS patients were treated with Interferon-β (n = 26), Teriflunomide (n = 22), Fingolimod (n = 11), Dimethyl fumarate (n = 11), Alemtuzumab (n = 9), Glatiramer acetate (n = 4) and others (n = 2).