Gibaldi M
Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle 98195, USA.
J Clin Pharmacol. 1997 Dec;37(12):1087-99. doi: 10.1002/j.1552-4604.1997.tb04292.x.
Estrogen replacement therapy (ERT) after menopause prevents the development of osteoporosis and reduces the risk of fracture. Other potential benefits are cardioprotection--probably related to the effects of estrogen on lipid profile and fibrinogen levels--and a delay in the onset of Alzheimer's disease and perhaps amelioration of the disease. ERT, however, increases the risk of endometriosis and endometrial cancer unless given with a progestin for at least 10 days per menstrual cycle. It also results in a small but real increase in breast cancer. Alendronate, a bisphosphonate, is the first serious competitor of conjugated equine estrogen for the treatment of osteoporosis. Nearing FDA approval are so-called designer estrogens (e.g., raloxifene), which may selectively prevent osteoporosis with little or no effects on endometrial and breast tissue.
绝经后雌激素替代疗法(ERT)可预防骨质疏松症的发生并降低骨折风险。其他潜在益处包括心脏保护作用——可能与雌激素对血脂和纤维蛋白原水平的影响有关——以及延迟阿尔茨海默病的发病,甚至可能改善病情。然而,ERT会增加子宫内膜异位症和子宫内膜癌的风险,除非每个月经周期联合使用孕激素至少10天。它还会使乳腺癌风险有小幅但实际的增加。阿仑膦酸钠,一种双膦酸盐,是共轭马雌激素治疗骨质疏松症的首个重要竞争对手。所谓的“设计雌激素”(如雷洛昔芬)即将获得美国食品药品监督管理局(FDA)批准,这类药物可能选择性地预防骨质疏松症,而对子宫内膜和乳腺组织几乎没有影响。