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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 >Comparative Effect of rhPTH(1-84) on Bone Mineral Density and Trabecular Bone Score in Hypoparathyroidism and Postmenopausal Osteoporosis
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Comparative Effect of rhPTH(1-84) on Bone Mineral Density and Trabecular Bone Score in Hypoparathyroidism and Postmenopausal Osteoporosis

机译:rhPth(1-84)对骨质酸碱性骨密度和绝经后骨质疏松症骨密度和小梁骨分数的比较作用

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摘要

Parathyroid hormone (PTH) (1-84) improves lumbar spine (LS) areal bone mineral density (aBMD) and trabecular bone score (TBS) in hypoparathyroidism over a 2-year treatment period. Studies in osteoporosis have shown that with PTH(1-34) there is a significant increase in LS aBMD and TBS. In this article, we provide new data comparing the effects of the same form of PTH, namely recombinant human PTH, rhPTH(1-84), on aBMD and TBS in hypoparathyroid and osteoporotic patients over an 18-month treatment period. We studied 19 premenopausal (mean age 45.8 +/- 11.8 years) and 16 postmenopausal (71 +/- 8.4 years) hypoparathyroid women and 38 women with postmenopausal osteoporosis (71 +/- 8.3 years). DXA (hologic) at LS, femoral neck, total hip, and distal one-third radius was assessed. Site-matched LS TBS data were extracted from deidentified spine DXA scans using the TBS iNsight software (version 2.1; Medimaps, Geneva, Switzerland). We observed a significant increase in LS aBMD in premenopausal and postmenopausal hypoparathyroid (3 +/- 1.1%, p 0.02 and 3.1 +/- 1.4%, p 0.05, respectively) and osteoporosis (6.2 +/- 1.1%, p 0.0001) patients after 18 months. There was a significant increase (3 +/- 1.5%, p = 0.05) in TBS in premenopausal hypoparathyroid patients. A change in TBS was not observed in either postmenopausal group. One-third radius aBMD significantly declined in postmenopausal hypoparathyroid (-3.6 +/- 1.1%, p 0.01) and osteoporosis (-8 +/- 1.4%, p 0.0001) patients. Overall, there was a significantly greater increase in TBS in premenopausal hypoparathyroid than in osteoporosis patients (p 0.0001) after adjusting for baseline values, age, BMI, and average daily dose of rhPTH(1-84). Comparing only postmenopausal women, the LS aBMD increase was greater in osteoporotic than hypoparathyroid subjects (p 0.01). Our results demonstrate that rhPTH(1-84) administered for 18 months increases trabecular aBMD in hypoparathyroidism and postmenopausal osteoporosis with greater gains observed in the subjects with osteoporosis. The data suggest different effects of PTH on bone depending on the baseline skeletal structure, skeletal dynamics, compartments, and menopausal status. (c) 2018 American Society for Bone and Mineral Research.
机译:甲状旁腺激素(第1-84页)(第1-84页)在2年治疗期间改善腰椎(LS)区域骨矿物密度(ABMD)和小梁病变中的小梁病变。骨质疏松症的研究表明,LS ABMD和TBS的PTH(1-34)显着增加。在本文中,我们提供了在18个月的治疗期间比较了在18个月的治疗期间对嗜症症和骨质疏松患者的相同形式的Pth,即重组人Pth,rhPth(1-84)的效果的新数据。我们研究了19个前肢(平均年龄45.8 +/- 11.8岁)和16次绝经后(71 +/- 8.4岁)患有绝经后骨质疏松症(71 +/- 8.3岁)的38名妇女。评估LS,股骨颈,总髋关节和远端三分之一半径的DXA(HOLOGIC)。使用TBS Insight软件(版本2.1版本2.1版本,日内瓦,瑞士Medimaps,日内瓦,瑞士)从De identified Spine DXA扫描中提取了网站匹配的LS TBS数据。我们观察到在前长期和绝经后尿胆露素(3 +/- 1.1%,P <0.02和3.1 +/- 1.4%,P <0.05)和骨质疏松症(6.2 +/- 1.1%)显着增加了LS ABMD P& 0.0001)患者18个月后。在前一代内前甲状腺素患者中,TBS在TBS中显着增加(3 +/- 1.5%,p = 0.05)。在绝经后群体中未观察到TBS的变化。后期半径ABMD在绝经后血清他羟吲哚(-3.6 +/- 1.1%,P&LT; 0.01)和骨质疏松症(-8 +/- 1.4%,P& 0.0001)患者中显着下降。总体而言,在调整基线值,年龄,BMI和平均日剂量的rhPth(1-84)的基线值(1-84)的基线值,年龄,BMI和平均每日剂量(1-84)的基线值后,TBS在骨质疏松症患者中显着增加仅比较绝经后妇女,骨质疏松症的增加大于骨盆大鼠(P <0.01)。我们的结果表明,rhPth(1-84)施用18个月的rhPth(1-84)增加了骨质疏松症的患者中的小梁ABMD,并且在骨质疏松症的受试者中观察到更大的收益的绝经后骨质疏松症。根据基线骨架结构,骨骼动态,隔室和更年期状态,数据表明PTH对骨骼上的不同影响。 (c)2018年美国骨骼和矿物学学会。

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