Effects of raloxifene and continuous combined hormone therapy on haemostasis variables: A multicenter, randomized, double-blind study

Abstract Introduction Hormone replacement therapy is known to increase the risk of thromboembolic events. We compared the effects of HRT and raloxifene on some haemostasis variables. Materials and methods In a multicenter, double-blind study, 54 healthy postmenopausal women were randomized to receiv...

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Veröffentlicht in:Thrombosis research 2007-01, Vol.119 (1), p.85-91
Hauptverfasser: Sgarabotto, Mariapaola, Baldini, Monica, Dei Cas, Alessandra, Manotti, Cesare, Luciana Barilli, Angela, Rinaldi, Maurizio, Benassi, Luigi, Bacchi Modena, Alberto
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Sprache:eng
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Zusammenfassung:Abstract Introduction Hormone replacement therapy is known to increase the risk of thromboembolic events. We compared the effects of HRT and raloxifene on some haemostasis variables. Materials and methods In a multicenter, double-blind study, 54 healthy postmenopausal women were randomized to receive either continuous treatment with 2 mg 17β-estradiol plus 1 mg norethisterone acetate ( n = 30) or 60 mg raloxifene ( n = 24) daily for 12 months. Blood samples were collected at baseline and at 3, 6 and 12 months to evaluate therapy effects on some haemostasis variables (factor VII, factor VIII, prothrombin fragments 1 and 2, protein C, protein C activity, protein S, thrombin–antithrombin complex, D-dimer, antithrombin, fibrinogen and plasminogen activator inhibitor). Results Both raloxifene and continuous combined hormone therapy modified the haemostasis variables toward a more prothrombotic profile. Factor VIII ( p < 0.01) and fibrinogen ( p < 0.05) plasma levels significantly increased at 6 months, prothrombin fragments 1 and 2 ( p < 0.05) significantly increased at 12 months, whereas protein C activity ( p < 0.001) and antithrombin ( p < 0.01) significantly decreased at 12 months in both groups. Conclusions Our results demonstrate that raloxifene and continuous combined hormone therapy exhibit the same prothrombotic profile. Both treatments induced an increase in procoagulant parameters at 6 months and a decrease in anticoagulant parameters at 12 months.
ISSN:0049-3848
1879-2472
DOI:10.1016/j.thromres.2006.01.001