Hormone therapy and venous thromboembolism among postmenopausal women -: Impact of the route of estrogen administration and progestogens:: The ESTHER study

被引:578
作者
Canonico, Marianne
Oger, Emmanuel
Plu-Bureau, Genevieve
Conard, Jacqueline
Meyer, Guy
Levesque, Herve
Trillot, Nathalie
Barrellier, Marie-Therese
Wahl, Denis
Emmerich, Joseph
Scarabin, Pierre-Yves
机构
[1] INSERM, U780, Cardiovasc Epidemiol Sect, F-94807 Villejuif, France
[2] Univ Paris 11, Villejuif, France
[3] Hop Cavale Blanche, Dept Med Interne, GETBO, Brest, France
[4] Univ Paris 05, Serv Hematol Biol, Hop Hotel Dieu, Paris, France
[5] Univ Paris 05, Fac Med, AP HP, Hop Europeen Georges Pompidou, Paris, France
[6] CHU Rouen, Dept Med Interne, Rouen, France
[7] CHUR, Inst Hematol Transfus, Lille, France
[8] CHU Cote Nacre, Serv Explorat Fonct, Caen, France
[9] CHU Nancy, Unite Med Interne Thrombose Malad Vasc, Hop Brabois, Vandoeuvre Les Nancy, France
[10] Univ Henri Poincare, INSERM, U734, Fac Med Nancy, Vandoeuvre Les Nancy, France
[11] Univ Paris 05, INSERM, U428, Paris, France
[12] Hop Europeen Georges Pompidou, Serv Med Vasc HTA, Paris, France
关键词
embolism; epidemiology; estrogens; progestogens; thrombosis;
D O I
10.1161/CIRCULATIONAHA.106.642280
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background - Oral estrogen therapy increases the risk of venous thromboembolism ( VTE) in postmenopausal women. Transdermal estrogen may be safer. However, currently available data have limited the ability to investigate the wide variety of types of progestogen. Methods and Results - We performed a multicenter case - control study of VTE among postmenopausal women 45 to 70 years of age between 1999 and 2005 in France. We recruited 271 consecutive cases with a first documented episode of idiopathic VTE ( 208 hospital cases, 63 outpatient cases) and 610 controls ( 426 hospital controls, 184 community controls) matched for center, age, and admission date. After adjustment for potential confounding factors, odds ratios ( ORs) for VTE in current users of oral and transdermal estrogen compared with nonusers were 4.2 ( 95% CI, 1.5 to 11.6) and 0.9 ( 95% CI, 0.4 to 2.1), respectively. There was no significant association of VTE with micronized progesterone and pregnane derivatives ( OR, 0.7; 95% CI, 0.3 to 1.9 and OR, 0.9; 95% CI, 0.4 to 2.3, respectively). In contrast, norpregnane derivatives were associated with a 4- fold- increased VTE risk ( OR, 3.9; 95% CI, 1.5 to 10.0). Conclusions - Oral but not transdermal estrogen is associated with an increased VTE risk. In addition, our data suggest that norpregnane derivatives may be thrombogenic, whereas micronized progesterone and pregnane derivatives appear safe with respect to thrombotic risk. If confirmed, these findings could benefit women in the management of their menopausal symptoms with respect to the VTE risk associated with oral estrogen and use of progestogens.
引用
收藏
页码:840 / 845
页数:6
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