巴泽多昔芬:一种治疗绝经后骨质疏松症的新型选择性雌激素受体调节剂。

Harry K Genant
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引用次数: 9

摘要

绝经后骨质疏松症需要安全有效的药物治疗,这给妇女和卫生保健系统都带来了沉重的负担。巴泽多昔芬是一种新型的选择性雌激素受体调节剂,具有独特的组织选择性。在近1万名绝经后妇女的3期临床试验中,与安慰剂相比,bazedoxifene显示出显著降低新椎体骨折的风险,对骨密度、骨转换标志物和脂质谱有有利影响。此外,在骨折风险增加的女性亚组中,与安慰剂和雷洛昔芬相比,巴泽多昔芬显著降低了非椎体骨折风险。巴泽多昔芬已被证明是安全且耐受性良好的,没有证据表明会刺激子宫内膜或乳房。这些数据表明,巴泽多昔芬可能为患有骨质疏松症或有骨质疏松风险的绝经后妇女提供显著的临床益处,这可能随后减轻该疾病的医疗和经济负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bazedoxifene: a new selective estrogen receptor modulator for postmenopausal osteoporosis.

An ongoing need for safe and effective pharmacological therapies exists for postmenopausal osteoporosis, which imposes a significant burden on both women and the health-care system. Bazedoxifene is a novel selective estrogen receptor modulator with a unique tissue-selectivity profile. In phase 3 clinical trials of nearly 10,000 postmenopausal women, bazedoxifene was shown to significantly reduce the risk of new vertebral fracture versus placebo, with favourable effects on bone mineral density, bone turnover markers and the lipid profile. Moreover, in a subgroup of women at increased risk of fracture, bazedoxifene significantly decreased non-vertebral fracture risk versus both placebo and raloxifene. Bazedoxifene has been shown to be safe and well tolerated, with no evidence of endometrial or breast stimulation. These data suggest that bazedoxifene may offer significant clinical benefit for postmenopausal women with or at risk of developing osteoporosis, which may subsequently lessen the medical and economic burden of this disease.

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