Obstetrical antiphospholipid syndrome: from the pathogenesis to the clinical and therapeutic implications

T Marchetti1, M Cohen, P de Moerloose

  • 1Laboratory of Hormonology, Maternity, Geneva University Hospitals, 1211 Geneva 14, Switzerland. tess.marchetti@hcuge.ch

Insights

Antiphospholipid syndrome (APS) in pregnancy poses risks like fetal loss and preeclampsia. Current treatments of low-dose aspirin and low-molecular weight heparin are insufficient for many patients, highlighting the need for new therapies.

Area of Science:

  • Obstetrics and Gynecology
  • Immunology
  • Hematology

Background:

  • Antiphospholipid syndrome (APS) is an acquired thrombophilia characterized by antiphospholipid antibodies (aPL).
  • Obstetrical APS presents significant risks to both mother and fetus, including recurrent pregnancy losses, stillbirth, intrauterine growth restriction (IUGR), and preeclampsia.
  • The pathogenesis involves aPL directly targeting trophoblastic cells through proapoptotic and proinflammatory pathways.

Purpose of the Study:

  • To review the clinical manifestations and pathogenesis of obstetrical Antiphospholipid syndrome.
  • To highlight the limitations of current first-line treatments for APS pregnancies.
  • To emphasize the urgent need for novel therapeutic strategies in managing APS during pregnancy.

Main Methods:

  • Literature review of obstetrical APS.
  • Analysis of pathogenic mechanisms of antiphospholipid antibodies.
  • Evaluation of current treatment efficacy and outcomes.

Main Results:

  • Obstetrical APS is associated with severe pregnancy complications.
  • Current treatments (low-dose aspirin and low-molecular weight heparin) fail in approximately 30% of cases.
  • Pathogenesis involves direct attack on trophoblastic cells via immune dysregulation.

Conclusions:

  • Obstetrical APS remains a complex condition with significant maternal and fetal morbidity.
  • Existing therapies are inadequate for a substantial portion of APS pregnancies.
  • Further research and development of new therapeutics are crucial for improving outcomes in APS pregnancies.

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