Table 2 Demographic and clinical features of APS patients with and without CNS manifestations.

From: Prevalence, risk factors, and prognosis of central nervous system manifestations in antiphospholipid syndrome

 

With CNS manifestations

(n = 119)

Without CNS manifestations

(n = 223)

P

Age at diagnosis (years)

49.7 ± 16.1

41.2 ± 15.7

 < 0.001

Male gender, n (%)

33 (27.7)

43 (19.1)

0.073

Disease duration (months)

10 (1, 48)

7 (1, 36)

0.033

Secondary APS, n (%)

75 (63.0)

90 (40.0)

 < 0.001

Extracranial arterial events, n (%)

52 (43.7)

72 (32.3)

0.037

Venous events, n (%)

49 (41.2)

85 (38.1)

0.638

Obstetric events, n (%)

25 (21.0)

104 (46.2)

 < 0.001

Livedo reticularis, n (%)

9 (7.6)

5 (2.2)

0.023

Diffuse alveolar hemorrhage, n (%)

1 (0.8)

0 (0)

1.000

APS nephropathy, n (%)

3 (2.5)

2 (0.9)

0.347

Thrombocytopenia, n (%)

46 (38.7)

58 (26.0)

0.015

Diabetes, n (%)

27 (22.7)

20 (8.9)

 < 0.001

Hypertension, n (%)

54 (45.4)

51 (22.7)

 < 0.001

Dyslipidaemia, n (%)

89 (74.8)

29 (12.9)

 < 0.001

Smoking, n (%)

22 (18.5)

30 (13.3)

0.217

Obesity, n (%)

10 (8.4)

23 (10.3)

0.569

aβ2GPI, n (%)

75 (63)

161 (71.6)

0.081

aCL, n (%)

90 (75.6)

149 (66.2)

0.091

LA, n (%)

88 (73.9)

141 (62.7)

0.045

Triple aPL positivity, n (%)

46 (38.7)

76 (34.1)

0.400

Antiplatelet drugs, n (%)

46 (38.7)

82 (36.4)

0.732

Anticoagulants, n (%)

53 (44.5)

148 (65.8)

 < 0.001

Corticosteroids, n (%)

99 (83.2)

155 (68.9)

0.006

Hydroxychloroquine, n (%)

60 (50.4)

167 (74.2)

 < 0.001

Immunosuppressants, n (%)

102 (85.7)

193 (86.5)

0.831

Statins, n (%)

15 (12.6)

131 (58.2)

 < 0.001

  1. Data were presented as the mean ± standard deviation, median (interquartile range) or n, where n = number of patients.
  2. APS antiphospholipid syndrome, CNS central nervous system, aβ2GPIs anti-β2 glycoprotein I antibodies, aCL anticardiolipin antibody, LA lupus anticoagulant, aPL antiphospholipid antibody.