Effect of raloxifene and clodronate on bone density in postmenopausal osteoporotic women.

P D'Amelio, M Muratore, F Tinelli, C Tamone, L Cosentino, E Quarta, F Calcagnile, G Carlo Isaia
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Abstract

The aim of the present study was to determine the safety and efficacy of combined therapy with raloxifene (RLX) and clodronate (CLD) in postmenopausal women. We enrolled 45 women with postmenopausal osteoporosis. The patients were randomly assigned to two different therapeutic groups: RLX 60 mg/day (n = 23) and RLX 60 mg/day plus CLD 100 mg intramuscularly (i.m.) once every 10 days (n = 22); 1 g of calcium and 800 IU of vitamin D3 were also given daily to both groups. Lumbar and femoral bone mineral density (BMD) were assessed at baseline and after 12 months of therapy using the dual X-ray absorptiometry technique (Norland XR36). We measured the bone turnover markers NTx and CTx, bone alkaline phosphatase (BAP) and osteocalcin at baseline and after 12 months of therapy. Our data demonstrate that 1 year of combined RLX+CLD therapy induced a higher increase in lumbar BMD than treatment with RLX alone as well as a major decrease in bone resorption markers, suggesting an additive effect of CLD on bone mass and inhibition of bone turnover. Furthermore, after 1 year of therapy levels of bone formation markers (osteocalcin and BAP) had increased in both groups, but the increase in osteocalcin and BAP was significantly higher in the RLX+CLD treated group, suggesting that, in addition to its inhibitory effects on resorption, CLD might also have stimulatory effects on mature osteoblast activity.

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雷洛昔芬和氯膦酸钠对绝经后骨质疏松妇女骨密度的影响。
本研究的目的是确定雷洛昔芬(RLX)和氯膦酸盐(CLD)联合治疗绝经后妇女的安全性和有效性。我们招募了45名绝经后骨质疏松症患者。患者被随机分配到两个不同的治疗组:RLX 60 mg/天(n = 23)和RLX 60 mg/天加CLD 100 mg肌肉注射(i.m)每10天一次(n = 22);两组每天也给予1克钙和800国际单位维生素D3。在基线和治疗12个月后,使用双x线吸收测量技术(Norland XR36)评估腰椎和股骨骨矿物质密度(BMD)。我们在基线和治疗12个月后测量骨转换标志物NTx和CTx,骨碱性磷酸酶(BAP)和骨钙素。我们的数据表明,与单独使用RLX治疗相比,RLX+CLD联合治疗1年的腰椎骨密度增加更高,骨吸收标志物显著减少,这表明CLD对骨量和骨转换的抑制具有附加作用。此外,治疗1年后,两组骨形成标志物(骨钙素和BAP)水平均升高,但RLX+CLD治疗组骨钙素和BAP的升高明显更高,这表明CLD除了抑制吸收作用外,还可能对成熟成骨细胞活性有刺激作用。
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