Mj. Cuadrado et al., ANTIPHOSPHOLIPID, ANTI-BETA-2-GLYCOPROTEIN-I AND ANTI-OXIDIZED-LOW-DENSITY-LIPOPROTEIN ANTIBODIES IN ANTIPHOSPHOLIPID SYNDROME, QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS, 91(9), 1998, pp. 619-626
Antiphospholipid antibodies (aPL), anti-beta 2-glycoprotein I (anti-be
ta 2-GPI) and anti-oxidized-low-density lipoprotein (LDL) antibodies a
ve all implicated in the pathogenesis of antiphospholipid syndrome. To
investigate whether different autoantibodies or combinations thereof
produced distinct effects related to their antigenic specificities, we
examined the frequencies of antiphospholipid syndrome (APS)-related f
eatures in the presence of different antibodies [aPL, beta 2-GPI, anti
-oxidized low density lipoprotein (LDL)] in 125 patients with APS. Med
ian follow-up was 72 months: 58 patients were diagnosed as primary APS
and 67 as APS pins systemic lupus erythematosus (SLE). Anticardiolipi
n antibodies (aCL), anti-beta 2-GPI and anti-oxidized LDL antibodies w
ere determined by ELISA; lupus anticoagulant (LA) by standard coagulom
etric methods. Univariate analysis showed that patients positive for a
nti-beta 2-GPI had a higher risk of recurrent thrombotic events (OR =
3.64, 95%CI, p = 0.01) and pregnancy loss (OR = 2.99, 95%CI, p = 0.004
). Patients positive for anti-oxidized LDL antibodies had a 2.24-fold
increase in the risk of arterial thrombosis (2.24, 95%CI, p = 0.03) an
d lower risk of thrombocytopenia (OR = 0.41 95%CI, p = 0.04). Patients
positive for aCL antibodies had a higher risk of pregnancy loss (OR =
4.62 95%CI, p = 0.001). When these data were tested by multivariate l
ogistic regression, the association between anti-beta 2-GPI and pregna
ncy loss and the negative association between anti-oxidized LDL antibo
dies and thrombocytopenia disappeared.