接受 rhPTH(1-84) 治疗的甲状旁腺功能减退症患者骨皮质内骨重塑过程中的短暂活化和从侵蚀到形成的过渡得到改善

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM JBMR Plus Pub Date : 2023-11-17 DOI:10.1002/jbm4.10829
Pernille van Dijk Christiansen, Tanja Sikjær, Christina Møller Andreasen, Jesper Skovhus Thomsen, Annemarie Brüel, Ellen Margrethe Hauge, Jean-Marie Delaisse, Lars Rejnmark, Thomas Levin Andersen
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引用次数: 0

摘要

在甲状旁腺功能减退症患者中,甲状旁腺激素(PTH)的缺乏会导致低血钙水平和骨重塑减少。使用重组人PTH(rhPTH)治疗可使骨转换恢复正常。本研究旨在探讨rhPTH(1-84)是否在30个月后继续激活皮质内骨重塑并促进从侵蚀到形成的转变,以及当rhPTH(1-84)停用时这种作用是否会短暂消失。研究人员对60例慢性甲状旁腺功能减退症患者(年龄在31至78岁之间)的骨活检组织进行了皮质组织形态测量,这些患者被随机分配到每天100微克的rhPTH(1-84)(n = 21)(PTH)或类似的安慰剂(n = 21)(PLB)中,为期6个月,作为常规治疗的补充。随后是开放标签延长期,患者延长rhPTH(1-84) (PTH)(5例),继续常规治疗(CON)(5例),或停用rhPTH(1-84),恢复常规治疗(PTHw),延长24个月(8例)。在第 6 个月(n = 42)和第 30 个月(n = 18)收集骨活检。6 个月和 30 个月后,PTH 组的整体皮质微结构(皮质孔隙率、厚度、孔密度和平均孔直径)与 PLB/CON 组和 PTHw 组没有差异。不过,PTH 组发生重塑的孔隙比例明显且持续高于 PLB/CON 组。与 PLB/CON 组相比,PTH 组正在进行骨形成的孔隙比例明显更高,而仅发生侵蚀的孔隙比例则没有差异。这导致形成孔和侵蚀孔之间的比例发生了变化,反映出 PTH 治疗组患者从侵蚀到形成的转变速度更快。在停用 rhPTH(1-84) 的 PTHw 组中,与 PLB/CON 组相比,PTH 的后一种效应被完全逆转。总之,甲状旁腺功能减退症患者的rhPTH(1-84)替代疗法可促进皮质内重塑及其从侵蚀向形成的转变,而不会影响整体皮质微结构。这种效应可持续至少30个月,并且在停止治疗时是可逆的。© 2023 作者。JBMR Plus 由 Wiley Periodicals LLC 代表美国骨与矿物质研究学会出版。
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Transitory Activation and Improved Transition from Erosion to Formation within Intracortical Bone Remodeling in Hypoparathyroid Patients Treated with rhPTH(1–84)

In hypoparathyroidism, lack of parathyroid hormone (PTH) leads to low calcium levels and decreased bone remodeling. Treatment with recombinant human PTH (rhPTH) may normalize bone turnover. This study aimed to investigate whether rhPTH(1–84) continued to activate intracortical bone remodeling after 30 months and promoted the transition from erosion to formation and whether this effect was transitory when rhPTH(1–84) was discontinued. Cortical histomorphometry was performed on 60 bone biopsies from patients (aged 31 to 78 years) with chronic hypoparathyroidism randomized to either 100 μg rhPTH(1–84) a day (n = 21) (PTH) or similar placebo (n = 21) (PLB) for 6 months as add-on to conventional therapy. This was followed by an open-label extension, where patients extended their rhPTH(1–84) (PTH) (n = 5), continued conventional treatment (CON) (n = 5), or withdrew from rhPTH(1–84) and resumed conventional therapy (PTHw) for an additional 24 months (n = 8). Bone biopsies were collected at months 6 (n = 42) and 30 (n = 18). After 6 and 30 months, the overall cortical microarchitecture (cortical porosity, thickness, pore density, and mean pore diameter) in the PTH group did not differ from that of the PLB/CON and PTHw groups. Still, the PTH group had a significantly and persistently higher percentage of pores undergoing remodeling than the PLB/CON groups. A significantly higher percentage of these pores was undergoing bone formation in the PTH compared with the PLB/CON groups, whereas the percentage of pores with erosion only was not different. This resulted in a shift in the ratio between formative and eroded pores, reflecting a faster transition from erosion to formation in the PTH-treated patients. In the rhPTH(1–84) withdrawal group PTHw, the latter effects of PTH were completely reversed in comparison to those of the PLB/CON groups. In conclusion, rhPTH(1–84) replacement therapy in hypoparathyroidism patients promotes intracortical remodeling and its transition from erosion to formation without affecting the overall cortical microstructure. The effect persists for at least 30 months and is reversible when treatment is withdrawn. © 2023 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.

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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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