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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 >Increases in BMD correlate with improvements in bone microarchitecture with teriparatide treatment in postmenopausal women with osteoporosis.
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Increases in BMD correlate with improvements in bone microarchitecture with teriparatide treatment in postmenopausal women with osteoporosis.

机译:绝经后骨质疏松妇女的骨密度增加与特立帕肽治疗改善骨微结构有关。

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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. INTRODUCTION: 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. MATERIALS AND METHODS: 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. RESULTS: 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). CONCLUSIONS: 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.
机译:特立帕肽治疗可使BMD的增加与2D和3D小梁微结构指标的改善相关。因此,改善小梁骨微结构可能是解释BMD增加如何在特立帕肽治疗期间改善骨强度的机制之一。简介:骨强度由BMD和其他骨骼质量要素(包括骨骼微结构)决定。特立帕肽治疗可增加BMD并改善皮质和小梁骨的微结构。特立帕肽治疗可使腰椎(LS)BMD升高约占椎骨骨折风险降低的30-41%。 BMD增加与皮质和小梁微体系结构改善之间的关系尚未进行研究。材料和方法:使用骨折预防试验中部分BMD测量值和经trans骨活检组织结构参数的患者亚组的数据,评估了特立帕肽治疗后BMD增加与皮质和小梁微体系改善之间的关系。在基线和12(n = 21)或22(n = 36)mo时测量2D组织形态计量学和3D microCT参数。在基线,12和18 mo评估LS BMD,在基线和12 mo评估股骨颈(FN)BMD。进行Pearson相关性以评估BMD的实际变化与微体系结构参数的实际变化之间的关系。结果:12个月时LS BMD的变化与22个月时小梁骨结构的改善显着相关:2D骨体积(r = 0.45,p = 0.02),2D平均壁厚(r = 0.41,p = 0.03),3D骨体积(r = 0.48,p = 0.006),3D小梁厚度(r = 0.44,p = 0.01),3D小梁分离(r = -0.37,p = 0.04),3D结构模型指数(r = -0.54,p = 0.001)和3D连接密度(r = 0.41,p = 0.02)。 18 mo时LS BMD的变化与22 mo时骨骼结构的改善具有相似的相关性。 12 mo时FN BMD的变化与2D平均壁厚(r = 0.56,p = 0.002),3D骨体积(r = 0.51,p = 0.004),3D小梁厚度(r = 0.44,p = 0.01),3D小梁分离(r = -0.46,p = 0.01)和3D结构模型索引(r = -0.55,p = 0.001)。结论:特立帕肽治疗患者骨骨密度的增加与小梁微结构的改善有关。因此,小梁骨微结构的改善可能是解释BMD增加如何在特立帕肽治疗期间改善骨强度的机制之一。

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