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地诺单抗和双膦酸盐对神经免疫性疾病患者糖皮质激素诱导的骨质疏松症的影响。

Effects of Denosumab and Bisphosphonates on Glucocorticoid-induced Osteoporosis in Patients with Neuroimmunological Disorders.

作者信息

Handa Hideo, Uzawa Akiyuki, Mori Masahiro, Yasuda Manato, Onishi Yosuke, Akamine Hiroyuki, Ogaya Etsuko, Niibe Yoko, Yokota Hajime, Kuwabara Satoshi

机构信息

Department of Neurology, Graduate School of Medicine, Chiba University, Japan.

Division of Pharmacy, Chiba University Hospital, Japan.

出版信息

Intern Med. 2025 Feb 15;64(4):543-549. doi: 10.2169/internalmedicine.3954-24. Epub 2024 Jul 11.

Abstract

Objective Although patients with neuroimmunological disorders often need to be treated with glucocorticoids and are at risk of developing glucocorticoid-induced osteoporosis, no research has focused on the treatment of glucocorticoid-induced osteoporosis in such patients. Methods We compared the efficacy of denosumab and bisphosphonates in glucocorticoid-induced osteoporosis in neuroimmunological diseases. In 57 patients with neuroimmunological disorders treated with corticosteroids (34 with neuromyelitis optica spectrum disorders, 16 with myasthenia gravis, and 7 with others), we retrospectively studied the long-term effects of denosumab (n=23) and bisphosphonates (n=34) on spine and total hip bone mineral density (BMD) measured by dual energy X-ray absorptiometry. Results There were no significant differences in the age, lumbar spine BMD, or mean dose or duration of prednisolone administration at baseline between the denosumab and bisphosphonate groups. During the follow-up period of up to 6 years, the increase in the lumbar spine and total hip BMD was greater in the denosumab group than in the bisphosphonate group (p<0.01). Insufficient bone fractures were observed in 2 (9%) of the 23 patients in the denosumab group and in 2 (6%) of the 34 patients in the bisphosphonate group (not significant). Conclusion Denosumab is more effective than bisphosphonates in increasing the BMD of patients with neuroimmunological disorders receiving glucocorticoids.

摘要

目的 尽管神经免疫性疾病患者常需接受糖皮质激素治疗,并有发生糖皮质激素诱导的骨质疏松症的风险,但尚无研究聚焦于此类患者糖皮质激素诱导的骨质疏松症的治疗。方法 我们比较了地诺单抗和双膦酸盐类药物在神经免疫性疾病糖皮质激素诱导的骨质疏松症治疗中的疗效。在57例接受皮质类固醇治疗的神经免疫性疾病患者中(34例视神经脊髓炎谱系障碍患者、16例重症肌无力患者和7例其他疾病患者),我们回顾性研究了地诺单抗(n = 23)和双膦酸盐类药物(n = 34)对通过双能X线吸收法测量的脊柱和全髋骨密度(BMD)的长期影响。结果 地诺单抗组和双膦酸盐组在年龄、腰椎BMD或基线时泼尼松龙给药的平均剂量或持续时间方面无显著差异。在长达6年的随访期内,地诺单抗组腰椎和全髋BMD的增加幅度大于双膦酸盐组(p<0.01)。地诺单抗组23例患者中有2例(9%)发生不完全骨折,双膦酸盐组34例患者中有2例(6%)发生不完全骨折(无显著差异)。结论 在增加接受糖皮质激素治疗的神经免疫性疾病患者的BMD方面,地诺单抗比双膦酸盐类药物更有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e84e/11904454/17f8fcc6f0c9/1349-7235-64-0543-g001.jpg

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