Am J Perinatol 1989; 6(2): 124-132
DOI: 10.1055/s-2007-999562
ORIGINAL ARTICLE

© 1989 by Thieme Medical Publishers, Inc.

Low-Dose Aspirin: Treatment for the Imbalance of Increased Thromboxane and Decreased Prostacyclin in Preeclampsia

Scott W. Walsh
  • Perinatal Physiology Research Unit, Department of Obstetrics, Gynecology, and Reproductive Sciences, and the Department of Physiology and Cell Biology, University of Texas Medical School at Houston, Houston, Texas
Further Information

Publication History

Publication Date:
04 March 2008 (online)

ABSTRACT

The discovery of the imbalance of increased thromboxane and decreased prostacyclin production in preeclamptic women has explained the cause of the major clinical symptoms of this disorder and has formed the basis and rationale for clinical studies with low-dose aspirin to treat preeclampsia. Low doses of aspirin (60 to 81 mg/day) have a remarkable ability to inhibit thromboxane production selectively without significantly inhibiting prostacyclin production. Therefore the actions of thromboxane to increase vasoconstriction, stimulate platelet aggregation, increase uterine contractility, and decrease uteroplacental blood flow are attenuated, and the ratio of thromboxane to prostacyclin is altered in favor of prostacyclin. Prostacyclin promotes vasodilation, inhibits platelet aggregation, decreases uterine contractility, and increases uteroplacental blood flow. The initial clinical studies with low doses of aspirin are very encouraging with respect to the treatment and prevention of preeclampsia. Substantial evidence already indicates that low-dose aspirin therapy decreases the incidence of preeclampsia; it decreases the maternal systemic arterial pressor response to angiotensin II; and it does not seem to be harmful to the fetus. Treatment of preeclampsia with prostacyclin appears to be contraindicated because prostacyclin is a potent systemic vasodilator and the clinical outcome of preeclamptic women infused with prostacyclin has been poor. The mechanism whereby low-dose aspirin preferentially inhibits thromboxane synthesis is not known. At the present time, treatment of preeclampsia with low-dose aspirin to inhibit thromboxane synthesis selectively without affecting prostacyclin synthesis appears most promising. If future studies do not reveal harmful effects, it is possible that the incidence of preeclampsia could be significantly reduced by placing women on low-dose aspirin therapy during pregnancy.