Division of Nephrology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
3D-SHAPER Medical, Barcelona, Spain.
Clin J Am Soc Nephrol. 2023 Sep 1;18(9):1195-1203. doi: 10.2215/CJN.0000000000000213. Epub 2023 Jun 14.
The effect of long-term denosumab therapy and of denosumab discontinuation on the cortical bone of the hip regions in dialysis patients has not been studied.
This retrospective study investigated the cortical and trabecular compartments and estimated strength indices of the hip region, obtained using 3D-SHAPER software, after a maximum of 5 years of denosumab therapy in 124 dialysis patients. A Wilcoxon signed-rank test was used to identify the differences in each parameter before and after denosumab initiation. Similarly, we investigated the changes in these parameters after denosumab discontinuation in 11 dialysis patients.
Integral and trabecular volumetric bone mineral densities (BMD) were significantly lower at the start of denosumab therapy than those in 1 year before denosumab initiation. After starting denosumab, areal BMD (median change +7.7% [interquartile range (IQR), +4.6 to +10.6]), cortical volumetric BMD (median change +3.4% [IQR, +1.0 to +4.7]), cortical surface BMD (median change +7.1% [IQR, +3.4 to +9.4]), and cortical thickness (median change +3.2% [IQR, +1.8 to +4.9]) showed a significantly higher trend for 3.5 years, which then stabilized at a higher value compared with baseline. A similar trend in the trabecular volumetric BMD (median change +9.8% [IQR, +3.8 to +15.7]) was observed over 2.5 years, with a higher value maintained thereafter. The whole area of the hip region improved after denosumab therapy. Similar trajectories were also found in the estimated strength indices. Conversely, at 1 year after denosumab discontinuation, these 3D parameters and estimated strength indices tended to largely worsen. The lateral aspect of the greater trochanter was the most pronounced location showing volumetric BMD loss.
The BMD of both cortical and trabecular components in the hip region was significantly higher after starting denosumab therapy. However, these measurements exhibited a trend of declining substantially after the discontinuation of denosumab.
尚未研究长期使用地舒单抗治疗以及停用地舒单抗对透析患者髋区皮质骨的影响。
本回顾性研究使用 3D-SHAPER 软件,对 124 例接受地舒单抗治疗最长达 5 年的透析患者的髋区皮质和松质骨容积及强度指数进行了研究。采用 Wilcoxon 符号秩检验比较地舒单抗治疗前后各参数的差异。同样,我们也研究了 11 例透析患者停用地舒单抗后这些参数的变化。
与地舒单抗治疗前 1 年相比,地舒单抗治疗开始时的整体和松质容积骨密度(BMD)明显较低。开始使用地舒单抗后,面积 BMD(中位数变化+7.7%[四分位距(IQR),+4.6 至+10.6])、皮质容积 BMD(中位数变化+3.4%[IQR,+1.0 至+4.7])、皮质表面 BMD(中位数变化+7.1%[IQR,+3.4 至+9.4])和皮质厚度(中位数变化+3.2%[IQR,+1.8 至+4.9])在 3.5 年内呈显著增高趋势,然后稳定在高于基线的水平。2.5 年内也观察到松质容积 BMD(中位数变化+9.8%[IQR,+3.8 至+15.7])呈相似的增高趋势,此后保持在较高水平。地舒单抗治疗后髋区的整个区域得到改善。估计的强度指数也出现了类似的轨迹。相反,停用地舒单抗 1 年后,这些 3D 参数和估计的强度指数趋于显著恶化。大转子外侧是体积 BMD 丢失最明显的部位。
开始使用地舒单抗治疗后,髋区皮质和松质骨的 BMD 显著增加。然而,这些测量值在停用地舒单抗后显示出显著下降的趋势。