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短期、高剂量甲状旁腺激素相关蛋白作为一种骨合成代谢剂用于治疗绝经后骨质疏松症。

Short-term, high-dose parathyroid hormone-related protein as a skeletal anabolic agent for the treatment of postmenopausal osteoporosis.

作者信息

Horwitz Mara J, Tedesco Mary Beth, Gundberg Caren, Garcia-Ocana Adolfo, Stewart Andrew F

机构信息

Division of Endocrinology, The University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.

出版信息

J Clin Endocrinol Metab. 2003 Feb;88(2):569-75. doi: 10.1210/jc.2002-021122.

Abstract

PTH-related protein (PTHrP) is homologous with PTH. PTH, an effective anabolic agent for treating osteoporosis, has been shown to stimulate both bone resorption by osteoclasts and bone formation by osteoblasts. We examined whether PTHrP might share anabolic properties in osteoporosis. A 3-month double-blind, prospective, placebo-controlled, randomized clinical trial was performed in 16 healthy postmenopausal women with osteoporosis. All received calcium and vitamin D, and all continued their prior hormone replacement therapy. One group also received daily sc PTHrP (6.56 microg/kg x d, or approximately 400 microg/d), and the other group received placebo injections. The PTHrP group displayed a 4.7% increase in lumbar spine bone mineral density (BMD) and also demonstrated an increase in osteoblastic bone formation, as assessed using serum osteocalcin measurements. In contrast, there was no increase in bone-specific alkaline phosphatase and collagen-1 propeptide or either of two markers of osteoclastic bone resorption, N-telopeptide, or deoxypyridinoline. One subject in the placebo group withdrew from the study, but there were no significant adverse events in the PTHrP group. PTHrP administered sc in high doses for only 3 months appears to be a potent anabolic agent, producing a 4.7% increase in lumbar spine BMD. This compares very favorably to available antiresorptive drugs for osteoporosis and is similar to the increases in BMD at this early time point reported for PTH. Despite the high doses, PTHrP was well tolerated. Larger clinical trials are required to confirm these results and fully assess the anabolic potential of PTHrP in osteoporosis.

摘要

甲状旁腺激素相关蛋白(PTHrP)与甲状旁腺激素(PTH)具有同源性。PTH是一种治疗骨质疏松症的有效促合成代谢药物,已被证明可刺激破骨细胞进行骨吸收以及成骨细胞进行骨形成。我们研究了PTHrP在骨质疏松症中是否也具有促合成代谢特性。对16名患有骨质疏松症的健康绝经后女性进行了一项为期3个月的双盲、前瞻性、安慰剂对照、随机临床试验。所有人都补充了钙和维生素D,并且都继续进行先前的激素替代疗法。一组每天皮下注射PTHrP(6.56微克/千克×天,约合400微克/天),另一组接受安慰剂注射。通过血清骨钙素测量评估,PTHrP组腰椎骨密度(BMD)增加了4.7%,并且成骨细胞骨形成也有所增加。相比之下,骨特异性碱性磷酸酶和I型胶原前肽没有增加,破骨细胞骨吸收的两个标志物N-端肽或脱氧吡啶啉也没有增加。安慰剂组有一名受试者退出了研究,但PTHrP组没有明显的不良事件。高剂量皮下注射PTHrP仅3个月似乎就是一种有效的促合成代谢药物,可使腰椎BMD增加4.7%。这与现有的用于治疗骨质疏松症的抗吸收药物相比非常有利,并且与报道的PTH在这个早期时间点的BMD增加情况相似。尽管剂量很高,但PTHrP的耐受性良好。需要进行更大规模的临床试验来证实这些结果,并全面评估PTHrP在骨质疏松症中的促合成代谢潜力。

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