McClung M R
a Oregon Osteoporosis Center , Portland , Oregon , USA.
Climacteric. 2015;18 Suppl 2:56-61. doi: 10.3109/13697137.2015.1104010. Epub 2015 Oct 27.
Albright was the first of many to show that loss of bone mass due to estrogen deficiency is an important part of the pathogenesis of postmenopausal osteoporosis. This led to the use of estrogen therapy which was shown to prevent bone loss at menopause and to reduce the risk of important fragility fractures. Selective estrogen receptor modulators (SERMs), with salutary estrogen-like skeletal effects and with protection from breast cancer, have important roles in the management of young postmenopausal women. New members of the SERM family may approach the effectiveness of estrogen in preventing bone loss and reducing fracture risk. When combined with estrogen, new SERMs prevent endometrial hyperplasia, and that combination reduces menopausal symptoms and prevents bone loss. Drugs that reduce bone turnover or stimulate bone formation by non-estrogen pathways have also been developed to treat osteoporosis. Emerging therapies, with unique mechanisms of action, may provide improved efficacy in treating women who already have osteoporosis.
奥尔布赖特是众多人中第一个表明雌激素缺乏导致的骨质流失是绝经后骨质疏松症发病机制的重要组成部分的人。这导致了雌激素疗法的应用,该疗法被证明可预防绝经后的骨质流失,并降低重要脆性骨折的风险。选择性雌激素受体调节剂(SERM)具有有益的雌激素样骨骼作用且能预防乳腺癌,在年轻绝经后女性的管理中发挥着重要作用。SERM家族的新成员在预防骨质流失和降低骨折风险方面可能接近雌激素的效果。当与雌激素联合使用时,新型SERM可预防子宫内膜增生,并且这种联合可减轻更年期症状并预防骨质流失。通过非雌激素途径减少骨转换或刺激骨形成的药物也已被开发用于治疗骨质疏松症。具有独特作用机制的新兴疗法可能在治疗已患有骨质疏松症的女性方面提供更高的疗效。