Recurrent pregnancy loss and its relation to FV Leiden, FII G20210A and polymorphisms of plasminogen activator and plasminogen activator inhibitor |
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Authors: | Wolf Cornelia E Haubelt Hannelore Pauer Hans Ulrich Hinney Bernd Krome-Cesar Claudette Legler Tobias J Hellstern Peter Emons Günter Zoll Barbara Köhler Michael |
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Institution: | Department of Transfusion Medicine, University of G?ttingen, G?ttingen, Germany. cwolf@med.uni-goettingen.de |
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Abstract: | Thrombophilic disorders and hypofibrinolysis were demonstrated to be risk factors in a majority of women with recurrent pregnancy loss (RPL) and infertility. We investigated the association of FV G1691A mutation, F II G20210A gene polymorphism (PM), 4G/5G PAI-1 and Alu I/D tPA PM in 32 women with infertility and 49 women with at least 2 unexplained early abortions. FV Leiden mutation was significantly more common in women with RPL (10%, p = 0.02) and infertility (19%, p = 0.0005) compared with controls (2%). PAI-1 4G PM and t-PA Alu I PM, alone or in combination, were not associated with RPL or infertility. 9/49 women with RPL showed coagulation disorders with heterozygous FV Leiden mutation (5), FXII (1), protein C (1) or protein S (2) deficiency. However, due to the small number of patients studied, no definite conclusion can be drawn. |
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