Boss S M, Huster W J, Neild J A, Glant M D, Eisenhut C C, Draper M W
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, USA.
Am J Obstet Gynecol. 1997 Dec;177(6):1458-64. doi: 10.1016/s0002-9378(97)70091-7.
We evaluated subtle endometrial morphologic changes in postmenopausal women assigned to placebo, raloxifene hydrochloride 200 or 600 mg/day, or conjugated estrogens (Premarin 0.625 mg/day) according to a new estrogenicity scoring system. Raloxifene, a new selective estrogen receptor modulator, was not expected to stimulate the endometrium.
Baseline and end point endometrial biopsies were performed during this double-blind, placebo-controlled 8-week study. A scoring system that was based on standard glandular and stromal morphologic criteria was used to quantitate estrogen-induced effects. Baseline, end point, and baseline-to-end point changes were analyzed for treatment differences.
Treatment groups were similar at baseline with most women showing no estrogenic effects. At end point, statistically significant moderate and marked estrogenic effects were noted in 77% of estrogen-treated women versus 15% of placebo-treated women versus 0% of raloxifene-treated women.
As expected, estrogen treatment stimulated postmenopausal endometrium. In contrast, raloxifene did not induce histopathologic evidence of endometrial stimulation in healthy postmenopausal women.
我们根据一种新的雌激素活性评分系统,评估了分配至安慰剂组、每日服用200毫克或600毫克盐酸雷洛昔芬组或结合雌激素组(每日服用0.625毫克倍美力)的绝经后女性子宫内膜的细微形态学变化。雷洛昔芬是一种新型选择性雌激素受体调节剂,预计不会刺激子宫内膜。
在这项为期8周的双盲、安慰剂对照研究中进行了基线和终点子宫内膜活检。使用基于标准腺体和间质形态学标准的评分系统来量化雌激素诱导的效应。分析了治疗差异的基线、终点以及基线至终点的变化。
各治疗组在基线时相似,大多数女性未显示出雌激素效应。在终点时,77%接受雌激素治疗的女性出现了具有统计学意义的中度和显著雌激素效应,而安慰剂治疗组为15%,雷洛昔芬治疗组为0%。
正如预期的那样,雌激素治疗刺激了绝经后子宫内膜。相比之下,雷洛昔芬在健康绝经后女性中未诱导出子宫内膜受刺激的组织病理学证据。