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Table 1 Demographic, clinical, and laboratory baseline characteristics of the 75 anti-beta2 glycoprotein I (aβ2GPI) IgG-positive patients and 20 healthy subjects (children)

From: Anti-phospholipid IgG antibodies detected by line immunoassay differentiate patients with anti-phospholipid syndrome and other autoimmune diseases

 

Primary thrombotic or obstetric APS (n = 34)

SARD (n = 41)

Healthy subjects (n = 20)

Sex, no. (%) female

31/34 (91%)

36/41 (88%)

9/20 (55%)

Autoimmune disease

34/34 (100%)

41/41 (100%)

0 (0%)

 Primary APS

34/34 (100%)

0 (0%)

0 (0%)

  SLE

0 (0%)

11/41 (27%)

0 (0%)

  SSj

0 (0%)

2/41 (5%)

0 (0%)

  SLE + SSj

0 (0%)

3/41 (7%)

0 (0%)

  DLE

0 (0%)

1/41 (2%)

0 (0%)

  PBC

0 (0%)

3/41 (7%)

0 (0%)

  SSc

0 (0%)

2/41 (5%)

0 (0%)

  DM/PM

0 (0%)

4/41 (10%)

0 (0%)

  UCTD

0 (0%)

15/41 (37%)

0 (0%)

 Thrombosis

19/34 (56%)

0 (0%)

0 (0%)

  Arterial

7/19 (37%)

0 (0%)

0 (0%)

  Venous

12/19 (63%)

0 (0%)

0 (0%)

 Obstetric manifestations

20/34 (59%)

0 (0%)

NA

  Pregnancy loss

15/20 (75%)

0 (0%)

NA

  Preeclampsia

5/20 (25%)

0 (0%)

NA

 Laboratory features

   

  LAC positivity

24/34 (71%)

18/41 (44%)

NP

  aβ2GPI IgG, median OD (25–75th percentile)

1.470 (0.929–1.747)

1.004 (0.655–1.298)

0.139 (0.047–0.444)

  aβ2GPI IgM, median OD (25–75th percentile)

0.350 (0.165–0.576)

0.450 (0.202–0.838)

0.088 (0.049–0.132)

  1. APS anti-phospholipid syndrome, aCL anti-cardiolipin antibodies, DLE discoid lupus erythematosus, DM/PM dermato/polymyositis, LAC lupus anti-coagulant, NA not applicable, NP not performed, OD optical density, PBC primary biliary cirrhosis, SARD systemic autoimmune rheumatic disease, SLE systemic lupus erythematosus, SSc systemic scleroderma, SjS Sjögren syndrome, UCTD undifferentiated connective tissue disease