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地舒单抗预防肺部疾病患者类固醇诱导性骨质疏松症的临床获益。

The clinical benefits of denosumab for prophylaxis of steroid-induced osteoporosis in patients with pulmonary disease.

机构信息

Matsusaka Municipal Hospital, Orthopaedic Surgery, Mie, Japan.

Matsusaka Municipal Hospital, Respiratory Center, Mie, Japan.

出版信息

Arch Osteoporos. 2017 Dec;12(1):44. doi: 10.1007/s11657-017-0336-1. Epub 2017 Apr 19.

Abstract

UNLABELLED

Previous reports demonstrated that bone density decreased rapidly during the initial few months of steroid therapy and continued decreasing at a rate of 2 to 4% annually. Our data indicates that denosumab can also play a role in the treatment of osteoporosis in the steroid-taking population.

INTRODUCTION

Respiratory physicians are often faced with the dilemma that long-term steroid use will deteriorate bone mineral density and quality. Previous reports demonstrated that bone density decreased 8 to 12% during the initial few months of steroid therapy then continued decreasing at a rate of 2 to 4% annually. Several prospective trials revealed that denosumab increased bone density in patients with osteoporosis [2-4] and decreased the rate of occurrence of fractures. The long-term efficacy of denosumab for glucocorticoid-induced osteoporosis, however, has not yet been proven.

MATERIALS

This has been an ongoing prospective study since 2014. In our respiratory centre, the first preventative measure used to combat glucocorticoid-induced osteoporosis (GIO) is oral bisphosphonates. Thirty-six patients were enlisted, and their treatment courses were changed from oral bisphosphonate, if administered, to the subcutaneous injection of denosumab 60 mg every 6 months, combined with a daily oral intake of DENOTAS® chewable combination tablets. The primary efficacy measures were changes in lumbar spine (LS) bone mineral density (BMD) and femoral BMD from baseline at 4, 8, 12 and 28 months.

RESULTS

At the 12-month follow-up, bone mineral density in the lumbar spine area of these patients increased by 3.2%, while bone mineral density in the hip area showed no significant increase. At the 28-month follow-up, 25 patients were still included in this study. Femoral BMD at 28 months increased significantly from the 12-month follow-up (P = 0.0259), though the first 12 months showed no significant increase. LS BMD continued to increase through the 28-month period.

CONCLUSIONS

Very little is known regarding the active prevention of GIO. Our data indicates that denosumab can play a promising role in the treatment of GIO.

摘要

目的

先前的报告表明,在类固醇治疗的最初几个月中,骨密度迅速下降,并且每年以 2%至 4%的速度继续下降。我们的数据表明,地舒单抗也可以在接受类固醇治疗的人群中治疗骨质疏松症。

方法

本研究为 2014 年开始的一项前瞻性研究。在我们的呼吸中心,对抗糖皮质激素诱导性骨质疏松症(GIO)的首要预防措施是口服双膦酸盐。共纳入 36 例患者,如果正在使用口服双膦酸盐,则将其治疗方案改为每 6 个月皮下注射地舒单抗 60mg,并联合每日口服 DENOTAS®咀嚼片。主要疗效指标为腰椎(LS)骨密度(BMD)和股骨 BMD 从基线到 4、8、12 和 28 个月的变化。

结论

对于 GIO 的主动预防,我们知之甚少。我们的数据表明,地舒单抗在 GIO 的治疗中可能发挥有前景的作用。

结论

地舒单抗还可以在接受类固醇治疗的人群中治疗骨质疏松症。

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