Lufkin E G, Whitaker M D, Nickelsen T, Argueta R, Caplan R H, Knickerbocker R K, Riggs B L
Division of Endocrinology and Metabolism, Mayo Clinic, Rochester, Minnesota 55905, USA.
J Bone Miner Res. 1998 Nov;13(11):1747-54. doi: 10.1359/jbmr.1998.13.11.1747.
Raloxifene is a selective estrogen receptor modulator that in experimental animals acts as an estrogen receptor antagonist in breast and endometrium but as an estrogen receptor agonist in the skeletal and cardiovascular systems. We conducted a 1-year prospective, randomized, double-blind trial in 143 postmenopausal osteoporotic women (mean +/- SD age, 68.4+/-5.0 years) with at least one prevalent vertebral fractures and low bone mineral density (BMD), comparing groups receiving raloxifene at 60 mg/day (RLX60) or 120 mg/day (RLX120) and a control group receiving supplements of 750 mg/day of calcium and 400 IU/day of vitamin D. There were no differences among groups in the occurrence of uterine bleeding, thrombophlebitis, breast abnormalities, or increased endometrial thickness (assessed by ultrasonography). As compared with controls, the changes in values over 1 year for RLX60 and RLX120, respectively, were significant for serum bone alkaline phosphatase (-14.9%, -8.87%), serum osteocalcin (-20.7%, -17.0%), and urinary C-telopeptide fragment of type I collagen/creatinine (-24.9%, -30.8%), markers of bone turnover; for serum total cholesterol (-7.0% for RLX60) and low density lipoprotein cholesterol (LDL) (-11.4% for RLX60) and for the LDL/HDL cholesterol ratio (-13.2%, -8.3%). BMD increased significantly in the total hip (1.66% for RLX60) and ultradistal radius (2.92%, 2.50%). There were nonsignificant trends toward increases over controls in BMD for lumbar spine, total body, and total hip (for RLX120). Using a >15% cutoff definition, raloxifene had no effect on incident fractures, but using a >30% cutoff, there was a dose-related reduction (p = 0.047). We conclude that raloxifene therapy is well tolerated, reduces serum lipids, and does not stimulate the uterus or breasts. It has beneficial effects on bone, although, under the conditions of this study, these appear to be of a smaller magnitude than have been reported with estrogen therapy.
雷洛昔芬是一种选择性雌激素受体调节剂,在实验动物中,它在乳腺和子宫内膜中作为雌激素受体拮抗剂起作用,但在骨骼和心血管系统中作为雌激素受体激动剂起作用。我们对143名绝经后骨质疏松女性(平均年龄±标准差为68.4±5.0岁)进行了一项为期1年的前瞻性、随机、双盲试验,这些女性至少有一处椎体骨折且骨密度较低。试验比较了接受60毫克/天雷洛昔芬(RLX60)或120毫克/天雷洛昔芬(RLX120)的组以及接受每日补充750毫克钙和400国际单位维生素D的对照组。各组在子宫出血、血栓性静脉炎、乳腺异常或子宫内膜厚度增加(通过超声检查评估)的发生率上没有差异。与对照组相比,RLX60和RLX120组在1年内血清骨碱性磷酸酶(分别为-14.9%,-8.87%)、血清骨钙素(-20.7%,-17.0%)和尿I型胶原C末端肽片段/肌酐(-24.9%,-30.8%)的变化显著,这些都是骨转换的标志物;血清总胆固醇(RLX60为-7.0%)、低密度脂蛋白胆固醇(RLX60为-11.4%)以及低密度脂蛋白/高密度脂蛋白胆固醇比值(-13.2%,-8.3%)也有显著变化。全髋部骨密度显著增加(RLX60为1.66%),桡骨远端超远端骨密度增加(2.92%,2.50%)。腰椎、全身和全髋部(RLX120组)的骨密度相对于对照组有不显著的增加趋势。采用大于15%的截断定义时,雷洛昔芬对新发骨折没有影响,但采用大于30%的截断定义时,存在剂量相关的降低(p = 0.047)。我们得出结论,雷洛昔芬治疗耐受性良好,可降低血脂,不刺激子宫或乳腺。它对骨骼有有益作用,不过,在本研究条件下,这些作用似乎比雌激素治疗所报道的要小。