Table 3

Analysis of baseline visits that occurred during trimesters 1 and 2 (n=53)

MarkerAPO (n=14)PE at any time (n=11)Preterm delivery (n=10)
T-test
(p value)
DOR
(95% CI)
T-test
(p value)
DOR
(95% CI)
T-test
(p value)
DOR
(95% CI)
ECR10.0512.33 (2.41 to 63.10)0.374.11 (0.88 to 19.27)0.0612.19 (2.30 to 64.72)
EC4d0.450.93 (0.25 to 3.46)0.183.89 (0.75 to 20.25)0.500.82 (0.19 to 3.48)
C30.870.38 (0.04 to 3.43)0.330.56 (0.06 to 5.11)0.850.64 (0.07 to 5.98)
C40.241.48 (0.37 to 5.97)0.740.70 (0.13 to 3.84)0.781.65 (0.35 to 7.82)
Anti-dsDNA0.731.05 (0.30 to 3.68)0.771.01 (0.27 to 3.83)0.700.96 (0.23 to 4.06)
LACNA0.90 (0.21 to 3.94)NA3.54 (0.86 to 14.58)NA1.70 (0.36 to 8.05)
Anti-PS/PT IgG0.181.53 (0.38 to 6.16)0.063.54 (0.86 to 14.58)0.113.11 (0.69 to 14.01)
aCL IgG0.531.53 (0.38 to 6.16)0.153.54 (0.86 to 14.58)0.233.11 (0.69 to 14.01)
Anti-β2-GP1 IgG0.471.04 (0.27 to 4.03)0.113.84 (0.96 to 15.31)0.382.13 (0.49 to 9.30)
  • DOR and p value determined by t-test for ECR1, EC4d, complement proteins C3 and C4, anti-dsDNA, LAC and antiphospholipid antibodies (anti-PS/PT, aCL and anti-β2-GP1) are reported. LAC results are provided as positive or negative. As the t-test could not be performed for LAC, p values are not reported for LAC (NA) in the table. PE at any time includes the pregnancies that presented with PE before (n=7) and after (n=4) the 36th week of gestation.

  • aCL, anticardiolipin; anti-dsDNA, anti-double-stranded DNA; anti-PS/PT, antiphosphatidylserine prothrombin complex; anti-β2-GP1, anti-β2 glycoprotein 1; APO, adverse pregnancy outcomes; DOR, diagnostic OR; EC4d, erythrocyte-bound C4d; ECR1, erythrocyte complement receptor 1; LAC, lupus anticoagulant; NA, not available; PE, pre-eclampsia.