Thromb Haemost 2000; 84(01): 9-14
DOI: 10.1055/s-0037-1613959
Commentary
Schattauer GmbH

Increased Fibrinolytic Activity during Use of Oral Contraceptives Is Counteracted by an Enhanced Factor XI-independent down Regulation of Fibrinolysis

A Randomized Cross-over Study of Two Low-dose Oral Contraceptives
Joost C. M. Meijers5
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, University Medical Center Utrecht, the Netherlands
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, University Medical Center Utrecht, the Netherlands
,
Saskia Middeldorp
3   Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
,
Winnie Tekelenburg
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, University Medical Center Utrecht, the Netherlands
,
Abraham E. van den Ende
3   Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
,
Guido Tans
4   Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands
,
Martin H. Prins
3   Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
,
Jan Rosing
4   Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands
,
Harry R. Büller
3   Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
,
Bonno N. Bouma
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, University Medical Center Utrecht, the Netherlands
1   From the Thrombosis and Haemostasis Laboratory, Department of Haematology, University Medical Center Utrecht, the Netherlands
› Author Affiliations

This study was supported in part by a grant from the Dutch Thrombosis Foundation. JCMM and HRB are Established Investigators of the Netherlands Heart Foundation (grants D96.021 and D93.013).
The authors thank the volunteers for participating in this study. The recruitment of volunteers and the collection of the materials under GCP-rules was performed by the foundation SorgSaem, Amsterdam (Dr. A. van Enk).
Further Information

Publication History

Received 21 October 1999

Accepted after resubmission 11 April 2000

Publication Date:
10 December 2017 (online)

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Summary

The effect of oral contraceptives (OC) on fibrinolytic parameters was investigated in a cycle-controlled cross-over study in which 28 non-OC using women were randomly prescribed either a representative of the so-called second (30 µg ethinylestradiol, 150 µg levonorgestrel) or third generation OC (30 µg ethinylestradiol, 150 µg desogestrel) and who switched OC after a two month wash out period. During the use of OC, the levels of tissue-type plasminogen activator (tPA) activity, plasminogen, plasmin-α2-antiplasmin complexes and D-dimer significantly increased (by 30 to 80%), while the levels of plasminogen activator inhibitor-1 (PAI-1) antigen, PAI-1 activity and tPA antigen significantly decreased (25 to 50%), suggesting an increase in endogenous fibrinolytic activity. These OC-induced changes were not different between the two contraceptive pills. TAFI (thrombin-activatable fibrinolysis inhibitor) levels increased on levonorgestrel, and even further increased on desogestrel. A clot lysis assay that probes both fibrinolytic activity and the efficacy of the coagulation system to generate thrombin necessary to down regulate fibrinolysis via TAFI showed no change of the clot lysis time during OC use. This finding suggests that the OC-induced increase in endogenous fibrinolytic activity is counteracted by an increased capacity of the coagulation system to down regulate fibrinolysis via TAFI. Indeed we observed that during OC use there was a significant increase of F1+2 generation during clot formation. When these assays were performed in the presence of an antibody against factor XI, we observed that the clot lysis time was significantly increased during OC use and that the increase in F1+2 generation during OC therapy was due to a factor XI-independent process, which was significantly higher on desogestrel than on levonorgestrel. These data indicate that the OC-induced inhibition of endogenous fibrinolysis takes place in a factor XI-independent way and is more pronounced on desogestrel than on levonorgestrel-containing OC.

5 Dr. J. C. M. Meijers, Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands