Suppr超能文献

激素疗法会影响年轻绝经后女性血浆中因子 VII 激活蛋白酶的水平。

Hormone therapy affects plasma measures of factor VII-activating protease in younger postmenopausal women.

机构信息

Unit for Thrombosis Research, Institute of Public Health, University of Southern Denmark, Niels Bohrs Vej 9, Esbjerg, Denmark.

出版信息

Climacteric. 2010 Aug;13(4):340-6. doi: 10.3109/13697131003597027.

Abstract

OBJECTIVES

Current reviews indicate that hormone therapy (HT) has a protective role in coronary heart disease (CHD) in younger postmenopausal women, whereas HT contributes to CHD in older women. Factor VII-activating protease (FSAP) is a serine protease that accumulates in unstable atherosclerotic plaques. FSAP is presumably involved in plaque stability and rupture. Reduced plasma concentration of FSAP may be associated with the development and expression of atherosclerosis and may thus contribute to precipitation of CHD. Here we address the potential influence of various HT regimens on plasma measures of FSAP in postmenopausal women treated for 1 year with different HT formulations or no HT.

METHODS

Six groups of postmenopausal women (n = 139) were allocated to five different HT modalities or no HT. Samples were collected at baseline and after 12 months of treatment. Prototype assays were used for the determination of FSAP antigen and FSAP activity.

RESULTS

The FSAP measures were comparable at baseline. No significant changes were observed in the control group after 12 months. HT in general induced a significant increase in FSAP antigen (7.7 microg/ml at baseline and 8.0 microg/ml after 12 months, p = 0.05), FSAP activity (1.54 PEU/ml at baseline and 1.68 PEU/ml after 12 months, p < 0.001) and FSAP ratio (202 mPEU/microg at baseline and 210 mPEU/microg after 12 months, p = 0.01).

CONCLUSIONS

HT increases the plasma measures of FSAP. This increase may contribute to the protective effect on CHD induced by HT in younger postmenopausal women.

摘要

目的

目前的综述表明,激素替代疗法(HT)对年轻绝经后女性的冠心病(CHD)具有保护作用,而 HT 则会导致老年女性 CHD。VII 因子激活蛋白酶(FSAP)是一种丝氨酸蛋白酶,在不稳定的动脉粥样硬化斑块中积聚。FSAP 可能参与斑块的稳定性和破裂。FSAP 血浆浓度降低可能与动脉粥样硬化的发生和表达有关,从而可能导致 CHD 的发生。在这里,我们研究了各种 HT 方案对接受不同 HT 制剂或不接受 HT 治疗 1 年的绝经后女性 FSAP 血浆水平的潜在影响。

方法

将 6 组绝经后妇女(n = 139)分为 5 种不同的 HT 方式或不接受 HT。在基线和治疗 12 个月后采集样本。使用原型测定法测定 FSAP 抗原和 FSAP 活性。

结果

基线时 FSAP 测量值相当。对照组在 12 个月后无明显变化。一般 HT 可显著增加 FSAP 抗原(基线时为 7.7 mcg/ml,12 个月后为 8.0 mcg/ml,p = 0.05)、FSAP 活性(基线时为 1.54 PEU/ml,12 个月后为 1.68 PEU/ml,p < 0.001)和 FSAP 比值(基线时为 202 mPEU/microg,12 个月后为 210 mPEU/microg,p = 0.01)。

结论

HT 增加 FSAP 的血浆水平。这种增加可能有助于解释 HT 在年轻绝经后女性中对 CHD 的保护作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验