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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Effects of alendronate on bone quality and remodeling in glucocorticoid-induced osteoporosis: a histomorphometric analysis of transiliac biopsies.
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Effects of alendronate on bone quality and remodeling in glucocorticoid-induced osteoporosis: a histomorphometric analysis of transiliac biopsies.

机译:阿仑膦酸盐对糖皮质激素诱导的骨质疏松症的骨质量和重塑的影响:经trans活检的组织形态计量学分析。

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摘要

Effects of alendronate (ALN) on bone quality and turnover were assessed in 88 patients (52 women and 36 men aged 22-75 years) who received long-term oral glucocorticoid exposure. Patients were randomized to receive oral placebo or alendronate 2.5, 5, or 10 mg/day for 1 year and stratified according to the duration of their prior glucocorticoid treatment. Transiliac bone biopsies were obtained for qualitative and quantitative analysis after tetracycline double-labeling at the end of 1 year of treatment. As previously reported in glucocorticoid-induced osteoporosis, low cancellous bone volume and wall thickness were noted in the placebo group as compared with normal values. Alendronate treatment was not associated with any qualitative abnormalities. Quantitative comparisons among the four treatment groups were performed after adjustment for age, gender, and steroid exposure. Alendronate did not impair mineralization at any dose as assessed by mineralization rate. Osteoid thickness (O.Th) and volume (OV/BV) were significantly lower in alendronate-treated patients, irrespective of the dose (P = 0.0003 and 0.01, respectively, for O.Th and OV/BV); however, mineral apposition rate was not altered. As anticipated, significant decreases of mineralizing surfaces (76% pooled alendronate group; P = 0.006), activation frequency (-72%; P = 0.004), and bone formation rate (-71%; P = 0.005) were also noted with alendronate treatment. No significant difference was noted between the changes observed with each dose. Absence of tetracycline label in trabecular bone was noted in approximately 4% of biopsies in placebo and alendronate-treated groups. Trabecular bone volume, parameters of microarchitecture, and resorption did not differ significantly between groups. In conclusion, alendronate treatment in patients on glucocorticoids decreased the rate of bone turnover, but did not completely suppress bone remodeling and maintained normal mineralization at all alendronate doses studied. Alendronate treatment did not influence the osteoblastic activity, which is already low in glucocorticoid-induced osteoporosis.
机译:在长期口服糖皮质激素暴露的88例患者(52名女性和36名男性,年龄22-75岁)中,评估了阿仑膦酸盐(ALN)对骨质量和周转的影响。患者随机接受口服安慰剂或阿仑膦酸盐2.5、5或10毫克/天,为期1年,并根据其先前糖皮质激素治疗的持续时间分层。在治疗的1年结束时,在四环素双标记后获得经bone骨活检,以进行定性和定量分析。如先前在糖皮质激素诱导的骨质疏松症中报道的,与正常值相比,安慰剂组的松质骨体积和壁厚低。阿仑膦酸盐治疗与任何定性异常无关。在调整年龄,性别和类固醇暴露后,对四个治疗组进行了定量比较。以矿化速率评估,阿仑膦酸盐不损害任何剂量的矿化。阿仑膦酸盐治疗的患者中类固醇厚度(O.Th)和体积(OV / BV)均显着降低,与剂量无关(O.Th和OV / BV分别为P = 0.0003和0.01);然而,矿物质的沉积率没有改变。如预期的那样,使用阿仑膦酸钠时,还注意到矿化表面(76%合并阿仑膦酸盐组; P = 0.006),激活频率(-72%; P = 0.004)和骨形成率(-71%; P = 0.005)显着减少。治疗。在每个剂量下观察到的变化之间没有发现显着差异。在安慰剂和阿仑膦酸盐治疗组中约有4%的活检中发现小梁骨中没有四环素标记。两组之间的小梁骨体积,微结构参数和吸收没有显着差异。总之,在所有研究剂量的阿仑膦酸盐中,对糖皮质激素患者使用阿仑膦酸盐治疗可降低骨转换率,但并未完全抑制骨重塑并保持正常矿化。阿仑膦酸盐治疗不影响成骨细胞活性,在糖皮质激素诱导的骨质疏松症中,该活性已经很低。

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