Plasma factor VII-activating protease is increased by oral contraceptives and induces factor VII activation in-vivo

Johannes J Sidelmann, Sven O Skouby, Cornelis Kluft, Ulrich Winkler, Frank Vitzthum, Herbert Schwarz, Jørgen Kristen Gram Holst, Jørgen Hjermind Jespersen

    8 Citationer (Scopus)

    Abstract

    Oral contraceptive (OC) use influences the hemostatic system significantly and is a risk factor for development of cardiovascular disease. Factor VII-activating protease (FSAP) has potential effects on hemostasis. The 1601GA genotype of the 1601G/A polymorphism in the FSAP gene expresses a FSAP alloenzyme with reduced pro-fibrinolytic activity. Presently, we address whether OC use and OC formulation affect FSAP measures in human blood. Healthy women (n=588) were allocated to six cycles of OCs with estrogen contents of 20µg (n=158), 30µg (n=284), 35µg (n=79) or 50µg (n=67) combined with various progestins. FSAP genotypes, FSAP and factor VII (FVII) plasma measures were assessed at baseline and after 6 cycles of OC. The 1601GA genotype was present in 49 (8.3%) of the women and was associated with significantly reduced levels of FSAP (P=0.001). OC use increased FSAP antigen by 25% and FSAP activity by 59% (P0.05). The relative increase in FSAP activity was significantly higher in women carrying the 1601GG genotype (63%) than in women carrying 1601GA genotype (50%) (P=0.01) and was associated with an increased activation of FVII. In conclusion: OC use increases the plasma measures of FSAP. The increase in FSAP is comparable in the seven OC-groups studied but is more significant in women carrying the 1601GG genotype than in women with the 1601GA genotype and results in increased activation of FVII suggesting that FSAP-induced activation of FVII takes place in-vivo and not only in-vitro as hitherto described.
    OriginalsprogEngelsk
    TidsskriftThrombosis Research
    Vol/bind128
    Udgave nummer5
    Sider (fra-til)e67-72
    ISSN0049-3848
    DOI
    StatusUdgivet - 1 nov. 2011

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