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共轭马雌激素、酯化雌激素、血栓前体变异与绝经后女性静脉血栓形成风险

Conjugated equine estrogen, esterified estrogen, prothrombotic variants, and the risk of venous thrombosis in postmenopausal women.

作者信息

Smith Nicholas L, Heckbert Susan R, Lemaitre Rozenn N, Reiner Alexander P, Lumley Thomas, Rosendaal Frits R, Psaty Bruce M

机构信息

Department of Epidemiology, University of Washington, Seattle, WA, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2006 Dec;26(12):2807-12. doi: 10.1161/01.ATV.0000245792.62517.3b. Epub 2006 Sep 14.

Abstract

BACKGROUND

Joint exposure to oral conjugated equine estrogen (CEE) and prothrombotic genetic variants factor II G20210A or factor V G1601A (Leiden) increase venous thrombotic risk 6- to 16-fold in postmenopausal women. Esterified estrogen (EE), an alternative estrogenic compound, appears not to be associated with increased risk and nothing is known about the joint risk with prothrombotic genetic variants.

METHODS AND RESULTS

We conducted a population-based, case-control study among postmenopausal women within a health maintenance organization. Subjects included 328 cases who sustained a first venous thrombosis and 1591 controls. Current hormone use was defined using electronic pharmacy records and variants FII G20210A and FV Leiden were genotyped using blood samples. FII and FV Leiden variants were associated with 2.1-fold and 3.7-fold increases in venous thrombotic risk, respectively. Overall, CEE use was associated with a 2.5-fold increase in risk compared with no hormone use, whereas EE use was not associated with a statistically increased risk. Compared with no hormone use and no variant, joint exposure to CEE and either prothrombotic variant was associated with an odds ratio (OR) of 9.1 (95% CI: 4.5 to 18.2), whereas joint exposure to EE and either variant was associated with an OR of 2.1 (0.6 to 6.8). When analyses were restricted to hormone users with either variant, CEE use was associated with an OR of 5.3 (1.3 to 21.7) compared with EE use.

CONCLUSIONS

These findings need replication and suggest EE use is associated with less risk than CEE use especially among 5% to 10% of women who are carriers of a prothrombotic variant.

摘要

背景

绝经后女性同时口服结合马雌激素(CEE)与促血栓形成基因变异因子II G20210A或因子V G1601A(莱顿突变)会使静脉血栓形成风险增加6至16倍。酯化雌激素(EE)作为一种替代雌激素化合物,似乎与风险增加无关,且对于其与促血栓形成基因变异的联合风险尚无了解。

方法与结果

我们在一个健康维护组织内对绝经后女性开展了一项基于人群的病例对照研究。研究对象包括328例首次发生静脉血栓的病例和1591例对照。通过电子药房记录确定当前激素使用情况,并利用血样对FII G20210A和FV莱顿突变进行基因分型。FII和FV莱顿突变分别使静脉血栓形成风险增加2.1倍和3.7倍。总体而言,与未使用激素相比,使用CEE使风险增加2.5倍,而使用EE未使风险有统计学意义的增加。与未使用激素且无突变相比,同时暴露于CEE和任一促血栓形成突变的比值比(OR)为9.1(95%置信区间:4.5至18.2),而同时暴露于EE和任一突变的OR为2.1(0.6至6.8)。当分析仅限于携带任一突变的激素使用者时,与使用EE相比,使用CEE的OR为5.3(1.3至21.7)。

结论

这些发现需要重复验证,提示与使用CEE相比,使用EE的风险更低,尤其是在5%至10%携带促血栓形成突变的女性中。

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