Sektion Biomedizinische Bildgebung, Klinik für Diagnostische Radiologie, Universitätsklinikum Schleswig-Holstein, Kiel, Germany.
J Bone Miner Res. 2013 Jun;28(6):1355-68. doi: 10.1002/jbmr.1870.
Data on treatment of glucocorticoid-induced osteoporosis (GIO) in men are scarce. We performed a randomized, open-label trial in men who have taken glucocorticoids (GC) for ≥3 months, and had an areal bone mineral density (aBMD) T-score ≤ -1.5 standard deviations. Subjects received 20 μg/d teriparatide (n = 45) or 35 mg/week risedronate (n = 47) for 18 months. Primary objective was to compare lumbar spine (L1 -L3 ) BMD measured by quantitative computed tomography (QCT). Secondary outcomes included BMD and microstructure measured by high-resolution QCT (HRQCT) at the 12th thoracic vertebra, biomechanical effects for axial compression, anterior bending, and axial torsion evaluated by finite element (FE) analysis from HRQCT data, aBMD by dual X-ray absorptiometry, biochemical markers, and safety. Computed tomography scans were performed at 0, 6, and 18 months. A mixed model repeated measures analysis was performed to compare changes from baseline between groups. Mean age was 56.3 years. Median GC dose and duration were 8.8 mg/d and 6.4 years, respectively; 39.1% of subjects had a prevalent fracture, and 32.6% received prior bisphosphonate treatment. At 18 months, trabecular BMD had significantly increased for both treatments, with significantly greater increases with teriparatide (16.3% versus 3.8%; p = 0.004). HRQCT trabecular and cortical variables significantly increased for both treatments with significantly larger improvements for teriparatide for integral and trabecular BMD and bone surface to volume ratio (BS/BV) as a microstructural measure. Vertebral strength increases at 18 months were significant in both groups (teriparatide: 26.0% to 34.0%; risedronate: 4.2% to 6.7%), with significantly higher increases in the teriparatide group for all loading modes (0.005 < p < 0.015). Adverse events were similar between groups. None of the patients on teriparatide but five (10.6%) on risedronate developed new clinical fractures (p = 0.056). In conclusion, in this 18-month trial in men with GIO, teriparatide showed larger improvements in spinal BMD, microstructure, and FE-derived strength than risedronate.
关于男性糖皮质激素诱导性骨质疏松症(GIO)治疗的数据很少。我们对已接受糖皮质激素(GC)治疗≥3 个月且骨密度(aBMD)T 评分≤-1.5 个标准差的男性进行了一项随机、开放标签试验。受试者接受 20μg/d 特立帕肽(n=45)或 35mg/周利塞膦酸盐(n=47)治疗 18 个月。主要目标是比较定量计算机断层扫描(QCT)测量的腰椎(L1-L3)骨密度。次要结局包括第 12 胸椎的高分辨率 QCT(HRQCT)测量的骨密度和微观结构、通过 HRQCT 数据的有限元(FE)分析评估的轴向压缩、前弯曲和轴向扭转的生物力学效应、双能 X 线吸收法测量的 aBMD、生化标志物和安全性。在 0、6 和 18 个月时进行计算机断层扫描。采用混合模型重复测量分析比较两组间的基线变化。平均年龄为 56.3 岁。GC 剂量和治疗时间的中位数分别为 8.8mg/d 和 6.4 年;39.1%的受试者存在既往骨折,32.6%的受试者接受了双膦酸盐治疗。18 个月时,两种治疗方法的小梁骨密度均显著增加,特立帕肽组的增加更为显著(16.3%对 3.8%;p=0.004)。两种治疗方法的 HRQCT 小梁和皮质变量均显著增加,特立帕肽组在整体和小梁骨密度以及骨表面积与体积比(BS/BV)等微观结构测量方面的改善更为显著。两组的椎体强度在 18 个月时均显著增加(特立帕肽:26.0%至 34.0%;利塞膦酸盐:4.2%至 6.7%),特立帕肽组在所有加载模式下的增加更为显著(0.005<p<0.015)。两组的不良事件相似。特立帕肽组无新发临床骨折(n=0),利塞膦酸盐组有 5 例(10.6%)新发临床骨折(p=0.056)。总之,在这项针对 GIO 男性的 18 个月试验中,特立帕肽在脊柱骨密度、微观结构和 FE 衍生强度方面的改善均大于利塞膦酸盐。