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罗莫佐单抗治疗成骨不全症骨质疏松症的疗效:一例报告。

Efficacy of romosozumab for osteoporosis in a patient with osteogenesis imperfecta: A case report.

机构信息

Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.

Department of Human Nutrition, Faculty of Human Nutrition, Tokyo Kasei Gakuin University, Tokyo, Japan.

出版信息

Mod Rheumatol Case Rep. 2022 Jan 7;6(1):128-133. doi: 10.1093/mrcr/rxab018.

Abstract

The efficacy of romosozumab for severe osteoporosis is uncertain in patients with osteogenesis imperfecta (OI). This report introduced a severe osteoporotic case of OI to examine the effect of romosozumab on bone fragility. A 64-year-old man with OI was referred to our department for finding out the cause of his repeated fractures. He was medicated with alendronate for only 1 year, 8 years ago, but it did not prevent repeated fractures, and thus, he had not received any treatments for osteoporosis since then. However, recently, the frequency of fractures had increased. At presentation, his lumbar and bilateral total hip bone mineral density (BMD) values were severely decreased to 0.546 and 0.209 g/cm2, respectively. Because of his severe osteoporosis, we started romosozumab treatment with eldecalcitol. Romosozumab (210 mg) was injected subcutaneously every month. At 12 months after drug initiation, his lumbar and total hip BMD increased by 22.0% and 136.4% versus pre-treatment levels, respectively. Bone formation markers increased, and bone resorption markers decreased at 12 months of the therapy. Neither hypocalcaemia nor any other severe adverse effects were observed in this severe osteoporotic case. This study revealed good responses of BMD and bone turnover markers to romosozumab treatment, which can be considered as an effective treatment option for osteoporotic OI patients.

摘要

罗莫佐单抗治疗成骨不全症(OI)重度骨质疏松的疗效尚不确定。本报告介绍了一例严重骨质疏松合并 OI 的病例,以评估罗莫佐单抗对骨脆弱性的影响。一位 64 岁男性,因反复骨折就诊于我科,患者有 OI 病史,8 年前曾服用阿仑膦酸钠治疗 1 年,但未能预防骨折再发,此后未再接受任何骨质疏松治疗。然而,最近骨折的频率增加。就诊时,其腰椎和双侧总髋部骨密度(BMD)值严重降低,分别为 0.546 和 0.209 g/cm2。鉴于其严重骨质疏松,我们开始使用骨化三醇和罗莫佐单抗治疗。罗莫佐单抗(210 mg)每月皮下注射 1 次。治疗开始后 12 个月,与治疗前相比,其腰椎和总髋部 BMD 分别增加了 22.0%和 136.4%。治疗 12 个月时,骨形成标志物增加,骨吸收标志物减少。在该严重骨质疏松病例中,未观察到低钙血症或其他严重不良反应。本研究显示罗莫佐单抗治疗对 BMD 和骨转换标志物有良好的反应,可作为骨质疏松合并 OI 患者的有效治疗选择。

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