Differential associations of oral estradiol and conjugated equine estrogen with hemostatic biomarkers

作者：Blondon M^*; Vlieg A Van Hylckama; Wiggins K L; Harrington L B; McKnight B; Rice K M; Rosendaal F R; Heckbert S R; Psaty B M; Smith N L

来源：Journal of Thrombosis and Haemostasis, 2014, 12(6): 879-886.

DOI：10.1111/jth.12560

• estradiol
• estrogens
• estrogen replacement therapy
• hemostasis
• thromboembolism
• venous thrombosis

Background The risk of venous thrombosis (VT) associated with oral hormone therapy (HT) may differ by type of estrogen compound. Objective To compare the thrombotic profile of women using oral conjugated equine estrogens (CEE) with that of women using oral estradiol (E2). Methods In postmenopausal, female, health maintenance organization (HMO) members with no history of VT, we measured thrombin generation, levels of factor VII activity, antithrombin activity and total protein S antigen. Mean levels of hemostasis biomarkers were cross-sectionally compared by use and type of estrogen using multiple linear regressions. The type of estrogen used was determined primarily by the HMO formulary, which changed its preferred estrogen from CEE to E2 during the study period. Results The sample included 92 E2 users and 48 CEE users, with a mean age of 64.1years and mean BMI of 29.1kgm-2. Twenty-seven per cent of HT contained medroxyprogesterone acetate. Compared with E2 users, CEE users had greater thrombin generation peak values and endogenous thrombin potential, and lower total protein S (multivariate adjusted differences of 49.8nm (95% CI, 21.0, 78.6), 175.0nmxMin (95% CI, 54.4, 295.7) and -13.4% (95% CI, -19.8, -6.9), respectively). Factor VII and antithrombin levels were not different between E2 and CEE users. Results were similar in subgroups of users of unopposed HT, opposed HT, low-dose estrogen and standard dose estrogen. Conclusion The hemostatic profile of women using CEE is more prothrombotic than that of women using E2. These findings provide further evidence for a different thrombotic risk for oral CEE and oral E2.

• 出版日期2014-6