Chen Peiqi, Miller Paul D, Recker Robert, Resch Heinrich, Rana Asad, Pavo Imre, Sipos Adrien A
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, USA.
J Bone Miner Res. 2007 Aug;22(8):1173-80. doi: 10.1359/jbmr.070413.
Increases in BMD are correlated with improvements in 2D and 3D trabecular microarchitecture indices with teriparatide treatment. Therefore, improvements in trabecular bone microarchitecture may be one of the mechanisms to explain how BMD increases improve bone strength during teriparatide treatment.
Bone strength is determined by BMD and other elements of bone quality, including bone microarchitecture. Teriparatide treatment increases BMD and improves both cortical and trabecular bone microarchitecture. Increases in lumbar spine (LS) BMD account for approximately 30-41% of the vertebral fracture risk reduction with teriparatide treatment. The relationship between increases in BMD and improvements in cortical and trabecular microarchitecture has not yet been studied.
The relationship between increases in BMD and improvements in cortical and trabecular microarchitecture after teriparatide treatment was assessed using data from a subset of patients who had areal BMD measurements and structural parameters from transiliac bone biopsies in the Fracture Prevention Trial. 2D histomorphometric and 3D microCT parameters were measured at baseline and 12 (n = 21) or 22 (n = 36) mo. LS BMD was assessed at baseline and 12 and 18 mo, and femoral neck (FN) BMD was measured at baseline and 12 mo. Pearson correlation was performed to assess the relationship between actual changes in BMD and actual changes in microarchitectural parameters.
Changes in LS BMD at 12 mo were significantly correlated with improvements in trabecular bone structure at 22 mo: 2D bone volume (r = 0.45, p = 0.02), 2D mean wall thickness (r = 0.41, p = 0.03), 3D bone volume (r = 0.48, p = 0.006), 3D trabecular thickness (r = 0.44, p = 0.01), 3D trabecular separation (r = -0.37, p = 0.04), 3D structural model index (r = -0.54, p = 0.001), and 3D connectivity density (r = 0.41, p = 0.02). Changes in LS BMD at 18 mo had similar correlations with improvements in bone structure at 22 mo. Changes in FN BMD at 12 mo were significantly correlated with changes in 2D mean wall thickness (r = 0.56, p = 0.002), 3D bone volume (r = 0.51, p = 0.004), 3D trabecular thickness (r = 0.44, p = 0.01), 3D trabecular separation (r = -0.46, p = 0.01), and 3D structural model index (r = -0.55, p = 0.001).
Increases in BMD are correlated with improvements in trabecular microarchitecture in iliac crest of patients with teriparatide treatment. Therefore, improvements in trabecular bone microarchitecture may be one of the mechanisms to explain how BMD increases improve bone strength during teriparatide treatment.
特立帕肽治疗后骨密度(BMD)的增加与二维和三维小梁微结构指数的改善相关。因此,小梁骨微结构的改善可能是解释特立帕肽治疗期间BMD增加如何提高骨强度的机制之一。
骨强度由BMD和骨质量的其他要素决定,包括骨微结构。特立帕肽治疗可增加BMD,并改善皮质骨和小梁骨的微结构。腰椎(LS)BMD的增加约占特立帕肽治疗使椎体骨折风险降低的30 - 41%。BMD增加与皮质骨和小梁微结构改善之间的关系尚未得到研究。
使用骨折预防试验中一部分患者的数据评估特立帕肽治疗后BMD增加与皮质骨和小梁微结构改善之间的关系,这些患者有髋部BMD测量值以及经髂骨活检的结构参数。在基线以及12个月(n = 21)或22个月(n = 36)时测量二维组织形态计量学和三维显微CT参数。在基线、12个月和18个月时评估LS BMD,在基线和12个月时测量股骨颈(FN)BMD。进行Pearson相关性分析以评估BMD的实际变化与微结构参数的实际变化之间的关系。
12个月时LS BMD的变化与22个月时小梁骨结构的改善显著相关:二维骨体积(r = 0.45,p = 0.02)、二维平均壁厚度(r = 0.41,p = 0.03)、三维骨体积(r = 0.48,p = 0.006)、三维小梁厚度(r = 0.44,p = 0.01)、三维小梁间距(r = -0.37,p = 0.04)、三维结构模型指数(r = -0.54,p = 0.001)和三维连接密度(r = 0.41,p = 0.02)。18个月时LS BMD的变化与22个月时骨结构的改善有类似的相关性。12个月时FN BMD的变化与二维平均壁厚度(r = 0.56,p = 0.002)、三维骨体积(r = 0.51,p = 0.004)、三维小梁厚度(r = 0.44,p = 0.01)、三维小梁间距(r = -0.46,p = 0.01)和三维结构模型指数(r = -0.55,p = 0.001)的变化显著相关。
特立帕肽治疗患者的髂嵴小梁微结构改善与BMD增加相关。因此,小梁骨微结构的改善可能是解释特立帕肽治疗期间BMD增加如何提高骨强度的机制之一。