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替勃龙或连续联合经皮雌二醇与醋酸甲羟孕酮对绝经后凝血因子及脂蛋白(a)的影响。

Effects of either tibolone or continuous combined transdermal estradiol with medroxyprogesterone acetate on coagulatory factors and lipoprotein(a) in menopause.

作者信息

Perrone G, Capri O, Galoppi P, Brunelli R, Bevilacqua E, Ceci F, Ciarla M V, Strom R

机构信息

Department of Gynecology and Obstetrics, University Sapienza, Rome, Italy.

出版信息

Gynecol Obstet Invest. 2009;68(1):33-9. doi: 10.1159/000211676. Epub 2009 Apr 7.

Abstract

BACKGROUND/AIM: The aim of this prospective controlled study was to compare the effects of two therapies for menopause on factor VII (FVII) and hemostatic variables.

METHODS

Postmenopausal women were assigned to receive one of the following treatments: transdermal estradiol (TTS E2; 50 microg) combined in a continuous sequential regimen with oral medroxyprogesterone acetate (MPA; 10 mg/day for 12 days) (group A; n = 20), tibolone (2.5 mg/day) (group B; n = 21) or placebo (group C; n = 19). Sixty women completed the 1-year treatment and underwent follow-up examinations after 3, 6 and 12 months.

RESULTS

TTS E2/MPA induced various changes in procoagulatory factors. At 12 months, fibrinogen, activated FVII (FVIIa) and coagulative FVII (FVIIc) had increased by 10.7, 12.9 and 3.7%, respectively. Among the fibrinolytic factors, plasminogen and alpha2-antiplasmin increased by 11.3 and 7.2%, respectively. Lipoprotein(a) [Lp(a)] and antithrombin III (ATIII) did not show any significant variation. Tibolone induced some changes toward a more homogeneous antithrombotic profile. Fibrinogen, FVIIa and FVIIc decreased significantly by 7.5, 8.1 and 21.3%, respectively. Plasminogen increased (by 11.8%) and Lp(a) decreased (by 28.4%). ATIII was unchanged with tibolone therapy.

CONCLUSION

Our results show that tibolone induces a significant reduction in FVIIc and Lp(a) and a greater enhancement of factors promoting fibrinolysis than the TTS E2/MPA regimen.

摘要

背景/目的:本前瞻性对照研究旨在比较两种绝经疗法对凝血因子VII(FVII)及止血变量的影响。

方法

绝经后女性被分配接受以下治疗之一:经皮雌二醇(TTS E2;50微克)与口服醋酸甲羟孕酮(MPA;每日10毫克,共12天)联合采用连续序贯疗法(A组;n = 20)、替勃龙(每日2.5毫克)(B组;n = 21)或安慰剂(C组;n = 19)。60名女性完成了1年的治疗,并在3、6和12个月后接受随访检查。

结果

TTS E2/MPA引起促凝血因子的多种变化。在12个月时,纤维蛋白原、活化FVII(FVIIa)和凝血FVII(FVIIc)分别增加了10.7%、12.9%和3.7%。在纤溶因子中,纤溶酶原和α2-抗纤溶酶分别增加了11.3%和7.2%。脂蛋白(a) [Lp(a)]和抗凝血酶III(ATIII)未显示任何显著变化。替勃龙引起了一些朝着更均匀抗血栓形成谱的变化。纤维蛋白原、FVIIa和FVIIc分别显著降低了7.5%、8.1%和21.3%。纤溶酶原增加(11.8%),Lp(a)降低(28.4%)。替勃龙治疗时ATIII无变化。

结论

我们的结果表明,与TTS E2/MPA方案相比,替勃龙可显著降低FVIIc和Lp(a),并更有效地增强促进纤溶的因子。

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