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. 2023 Aug 3;11(8):2192. doi: 10.3390/biomedicines11082192

Table 2.

Clinical and serological characteristics of the study subgroups.

Primary APS Secondary APS p-Values OR (95% CI)
Number of patients 30 42
Gender Male 6 4 0.21 0.42 (0.10–1.64)
Female 24 38
Deep venous thrombosis 14 16 0.46 0.70 (0.27–1.81)
Recurrent deep venous thrombosis 7 4 0.11 0.34 (0.09–1.31)
Arterial thrombosis 7 17 0.13 2.23 (0.78–6.36)
Recurrent arterial thrombosis 1 8 0.07 6.82 (0.80–57.82)
Obstetric morbidity 6 11 0.54 1.41 (0.45–4.38)
Deep venous thrombosis + Arterial thrombosis 0 6 0.22 3.91 (0.43–35.41)
Deep venous thrombosis + Obstetric morbidity 1 3 0.49 2.23 (0.22–22.55)
Arterial thrombosis + Obstetric morbidity 0 3 0.49 2.23 (0.22–22.55)
Deep venous thrombosis + Arterial thrombosis + Obstetric morbidity 0 2 0.56 1.05 (0.98–1.12)
Non-thrombotic manifestations (such as livedo, vegetation, migraine, convulsions) 11 14 0.76 0.86 (0.32–2.30)
Serology at the time of diagnosis aCL 6 9 0.88 1.09 (0.34–3.47)
aβ2GPI 9 10 0.55 0.72 (0.25–2.09)
LAC 30 42
aCL + aβ2GPI 2 5 0.46 1.89 (0.34–10.47)
aCL + LAC 6 9 0.88 1.09 (0.34–3.47)
aβ2GPI + LAC 9 10 0.55 0.72 (0.25–2.09)

APS—antiphospholipid syndrome; aCL—anti-cardiolipin antibodies; aβ2GPI—anti-β2 glycoprotein I antibodies; LAC—lupus anticoagulant.