Inherited thrombophilia in women with poor aPL-related obstetric history: prevalence and outcomes. Survey of 208 cases from the European Registry on Obstetric Antiphospholipid Syndrome cohort

Am J Reprod Immunol. 2016 Aug;76(2):164-71. doi: 10.1111/aji.12534.

Abstract

Aim: To analyse the prevalence and effects of inherited thrombophilic disorders (ITD) on maternal-foetal outcomes in cases of antiphospholipid antibody related to obstetric complications.

Methods: Women with obstetric complaints who tested positive for aPL and with inherited thrombophilia were prospectively and retrospectively included.

Results: ITD data were available in 208 of 338: 147 had obstetric antiphospholipid syndrome (OAPS) and 61 aPL-related obstetric morbidity (OMAPS). 24.1% had ITD. Laboratory categories I and IIa were more related to OAPS-ITD and IIb and IIc to OMAPS-ITD. No significant differences in obstetric complaints were observed. Regarding ITD carriers, treatment rates were higher in OAPS than in OMAPS for LMWH and LDA plus LMWH (P=.002).

Conclusion: Cases with aPL-related OAPS/OMAPS showed no differences in maternal-foetal outcomes regardless of the presence of one ITD. Maternal thrombotic risk was low, with ITD-positive cases included. Registry data concur with Sydney criteria, whereby aPL-ITD-positive patients are classified as having antiphospholipid syndrome.

Keywords: antiphospholipid antibody; inherited thrombophilia; obstetric outcome; thrombosis; treatment.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiphospholipid Syndrome / complications
  • Antiphospholipid Syndrome / epidemiology*
  • Europe / epidemiology
  • Female
  • Humans
  • Pregnancy
  • Pregnancy Complications, Hematologic / epidemiology*
  • Pregnancy Outcome / epidemiology*
  • Prevalence
  • Registries*
  • Thrombophilia / complications
  • Thrombophilia / epidemiology*

Supplementary concepts

  • Familial antiphospholipid syndrome