Effects of anticoagulation protein defect in maternal plasma on spontaneous abortion

Chin Med Sci J. 2004 Dec;19(4):290-2.

Abstract

Objective: To investigate the mechanism of anticoagulation protein defect in the pathogenesis of unexplained recurrent miscarriage.

Methods: Fifty-seven patients with a history of unexplained abortion were enrolled as the investigation group for tests of protein C, protein S, antithrombin III (AT-III), as well as activated protein C resistance (APC-R). The control group consisted of fifty healthy women with a history of normal pregnancy and delivery. Blood samples were obtained for, measuring serum activity of protein C, protein S, AT-III, and APC-R. Patients with positive APC-R were tested for factor V (FV) Leiden gene mutation by PCR-RFLP method.

Results: Of the 57 patients, 12 (21.1%), 1 (1.8%), and 5 (8.8%) cases were found with protein S, protein C, and AT-III deficiency respectively, and 13 (22.8%) cases with positive results of APC-R. Of the control group, no protein C or AT-III deficiency was ever found, whereas 2 (4.0%) volunteers were presented with protein S deficiency and 3 (6.0%) with positive results of APC-R. No FV Leiden gene mutation was identified in all the patients with positive APC-R results. Late spontaneous abortion cases had higher incidence of anticoagulation protein defect than the early cases.

Conclusion: Anticoagulation protein defect may play a role in the pathogenesis of fetal loss, especially for those occurring in late stage of pregnancy.

MeSH terms

  • Abortion, Habitual / blood
  • Abortion, Habitual / etiology*
  • Activated Protein C Resistance / blood
  • Activated Protein C Resistance / complications*
  • Activated Protein C Resistance / genetics
  • Adult
  • Antithrombin III / metabolism
  • Antithrombin III Deficiency / blood
  • Antithrombin III Deficiency / complications*
  • Factor V / genetics
  • Female
  • Humans
  • Point Mutation
  • Protein C / metabolism
  • Protein C Deficiency / blood
  • Protein C Deficiency / complications*
  • Protein S / metabolism
  • Protein S Deficiency / blood
  • Protein S Deficiency / complications*

Substances

  • Protein C
  • Protein S
  • factor V Leiden
  • Antithrombin III
  • Factor V