Summary
We investigated the association between inherited and acquired maternal thrombophilias
and adverse pregnancy events. A cohort of 491 patients with a history of adverse pregnancy
outcomes was evaluated for activated protein C resistance, factor V Leiden and prothrombin
G20210A mutations, hyperhomocysteinemia, deficiencies of antithrombin, protein C and
S and both anticardiolipin antibodies and lupus anticoagulants. The study had an 80%
power to detect a 15% difference in the prevalence of thrombophilia for 1st trimester
loss. In our high-risk cohort the presence of 1 maternal thrombophilia or more than
one thrombophilia were found to be protective of recurrent losses at < 10 weeks (1
thrombophilia: OR: 0.55, 95% CI: 0.33–0.92; >1 thrombophilia: OR: 0.48, 95%CI:0.29–0.78).
In contrast, the presence of maternal thrombophilia(s) was modestly associated with
an increased risk of losses ≥ 10 weeks (1 thrombophilia: OR:1.76, 95%CI: 1.05–2.94,
>1 thrombophilia: OR:1.66, 95%CI:1.03–2.68). Women who experienced only euploid losses
were not more likely to have an identified thrombophilia than women who experienced
only aneuploid losses (OR 1.03; 0.38–2.75). The presence of maternal thrombophilia
was associated with an increased risk of fetal loss after 14 weeks, fetal growth restriction,
abruption and preeclampsia. There was a significant “dose-dependent” increase in the
risk of abruption (OR:3.60, 95%CI: 1.43–9.09) and preeclampsia (OR:3.21, 95%CI:1.20–8.58).
In conclusion, these data indicate maternal thrombophilias are not associated with
pregnancy wastage prior to 10 weeks of gestation.
Keywords
Maternal thrombophilia - recurrent abortion - fetal loss