Thromb Haemost 2006; 95(04): 606-611
DOI: 10.1160/TH05-10-0684
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Hyperprothrombinaemia-induced APC resistance: Differential influence on fibrin formation and fibrinolysis

Bianca M. Binetti
1   Department of Biomedical Sciences, Section of General Pathology, University of Bari, Italy
,
Crescenza Rotunno
1   Department of Biomedical Sciences, Section of General Pathology, University of Bari, Italy
,
Armando Tripodi
2   Angelo Bianchi Bonomi, Hemophilia and Thrombosis Center, Department of Internal Medicine, University and IRCCS Maggiore Hospital, Milano, Italy
,
Daniela Asti
2   Angelo Bianchi Bonomi, Hemophilia and Thrombosis Center, Department of Internal Medicine, University and IRCCS Maggiore Hospital, Milano, Italy
,
Fabrizio Semeraro
1   Department of Biomedical Sciences, Section of General Pathology, University of Bari, Italy
,
Nicola Semeraro
1   Department of Biomedical Sciences, Section of General Pathology, University of Bari, Italy
,
Mario Colucci
1   Department of Biomedical Sciences, Section of General Pathology, University of Bari, Italy
› Author Affiliations

Financial support: Supported by a grant from Ministero della Università e della Ricerca Scientifica e Tecnologica (ex 60%).
Further Information

Publication History

Received 19 October 2005

Accepted after revision 25 February 2006

Publication Date:
30 November 2017 (online)

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Summary

The prothrombin gene mutation G20210A is a common risk factor for thrombosis and has been reported to cause APC resistance. However, the inhibition of thrombin formation by APC not only limits fibrin formation but also stimulates fibrinolysis by reducing TAFI activation. We evaluated the influence of prothrombin G20210A mutation on the anticoagulant and fibrinolytic activities of APC (1 µg/ml). Thirtytwo heterozygous carriers and 32 non carriers were studied. APC anticoagulant activity was assessed by aPTT prolongation whereas APC fibrinolytic activity was determined by a microplate clot lysis assay. APC-induced aPTT prolongation was markedly less pronounced in carriers than in non carriers. On the contrary, fibrinolysis time was shortened by APC to a comparable extent in both groups. Accordingly, prothrombin levels were strongly correlated with APC-induced aPTT prolongation but not with APC-induced shortening of lysis time. The addition of purified prothrombin to normal plasma (final concentration 150%) caused APC resistance in the clotting assay over the whole range of tested APC concentrations (0.125–1.5 µg/ml). In the fibrinolytic assay, instead, prothrombin supplementation made the sample resistant to low but not to high concentrations of APC (>0.5 µg/ml). Thrombin and TAFIa determination in the presence of 1 µg/ml APC revealed that hyperprothrombinemia, although capable of enhancing thrombin generation, was unable to induce detectable TAFIa formation. It is suggested that APC resistance caused by hyperprothrombinaemia does not translate in impaired fibrinolysis, at least in the presence of high APC levels, because the increase in thrombin formation is insufficient to activate the amount of TAFI required to inhibit plasminogen conversion. These data might help to better understand the relationship between thrombin formation and fibrinolysis down-regulation.