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The action of ovarian hormones in cardiovascular disease

机译:卵巢激素在心血管疾病中的作用

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The incidence of cardiovascular disease (CAD) differs between men and women, in part because of differences in risk factors and hormones. This sexual dimorphism means a lower incidence in atherosclerotic diseases in premenopausal women, which subsequently rises in postmenopausal women to eventually equal that of men. These observations point towards estrogen and progesterone playing a lifetime protective role against CAD in women. As exogenous estrogen and estrogen plus progesterone preparations produce significant reductions in low-density lipoprotein (LDL) cholesterol levels and significant increases in high-density lipoprotein (HDL) cholesterol, this should in theory lower the risk of CAD. However, results from oral contraceptive (OC) use and combined estrogen and progesterone hormone replacement therapy (HRT) have suggested that hormone replacement regimes do not provide cardiovascular protection. In fact, depending on the preparation and the presence or absence of genetic risk factors, an increased risk of cardiovascular diseases such as venous thrombosis, myocardial infarction (MI) and stroke have been observed. Interestingly, in the majority of studies the increase in risk was highest in the first year, after which an increase in risk was not observed, and in some studies a lower risk of CAD was evident after four or five years of exogenous hormone administration. While the debate continues about the merits of HRT, and several good reviews exist on the statistics of CAD in relation to exogenous hormones, we have decided to review the literature to piece together the physiological actions of estrogen and progesterone preparations on the individual mechanistic components leading to CAD; namely, the altered endothelium and the haemostatic balance between coagulation and fibrinolysis. We present possible mechanisms for how HRT and OCs protect against MI in the absence of cardiovascular risk factors but increase the incidence of MI in their presence. We also speculate on the roles played by hormones on the short- and long-term risks of cardiovascular disease.
机译:男性和女性之间心血管疾病(CAD)的发生率有所不同,部分原因是危险因素和激素的差异。这种性别差异意味着绝经前妇女的动脉粥样硬化疾病发病率较低,而绝经后妇女的动脉粥样硬化病发病率随后上升,最终与男子相等。这些观察结果表明,雌激素和孕酮在女性中对CAD起到终生保护作用。由于外源性雌激素和雌激素加孕酮制剂可显着降低低密度脂蛋白(LDL)胆固醇水平,并显着增加高密度脂蛋白(HDL)胆固醇,因此从理论上讲,这应降低CAD的风险。但是,口服避孕药(OC)的使用以及雌激素和孕激素激素替代疗法(HRT)的联合使用的结果表明,激素替代方案不能提供心血管保护。实际上,根据制备方法以及是否存在遗传危险因素,已经观察到心血管疾病(如静脉血栓形成,心肌梗塞(MI)和中风)的风险增加。有趣的是,在大多数研究中,风险增加在第一年最高,此后未观察到风险增加,并且在某些研究中,外源激素给药四到五年后,CAD的风险明显降低。尽管有关HRT优点的争论仍在继续,关于外源激素的CAD统计数据已有一些不错的评论,但我们决定回顾一下文献,将雌激素和孕激素制剂的生理作用整合到各个机制上。到CAD;即,内皮的改变和凝血与纤维蛋白溶解之间的止血平衡。我们提出了在没有心血管危险因素的情况下,HRT和OCs如何预防MI的可能机制,但在它们存在时增加MI的发生率。我们还推测激素在心血管疾病的短期和长期风险中所起的作用。

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