Coagulation factor V and thrombophilia: Background and mechanisms

Kenneth Segers; Björn Dahlbäck; Gerry A. F. Nicolaes

doi:10.1160/TH07-02-0150

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2007; 98(03): 530-542
DOI: 10.1160/TH07-02-0150

Theme Issue Article

Schattauer GmbH

Coagulation factor V and thrombophilia: Background and mechanisms

Authors

Kenneth Segers

¹Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands
Björn Dahlbäck

²Department of Laboratory Medicine, Clinical Chemistry, Lund University, Wallenberg Laboratory, University Hospital, Malmö, Sweden
Gerry A. F. Nicolaes

¹Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands

Abstract

Summary

Human coagulation factor V (FV) is an essential coagulation protein with functions in both the pro- and anticoagulant pathways. Failure to express and control FV functions can either lead to bleeding, or to thromboembolic disease. Both events may develop into a life-threatening condition. Since the first description of APC resistance, and in particular the description of the so-called factor V_Leiden mutation, in which a prominent activated protein C cleavage site in FV has been abolished through a mutation in the FV gene, FV has been in the center of attention of thrombosis research. In this review we describe how the functions of FV are expressed and regulated and provide an extensive description of the role that FV plays in the etiology of thromboembolic disease.

Keywords

Factor V - coagulation - thrombosis - thrombophilia - protein C pathway

Full Text

References

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