Biological therapy for osteoporosis - solving clinical problems - a case report

T. Janković, A. Savić, J. Zvekic-Svorcan, Marina Maksimovic-Simovic, K. Boskovic
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Abstract

Introduction. Elucidation of the pathogenetic mechanisms of osteoporosis has led to the development of new and effective drugs from the group of biological agents. Case report. In April 2018, a 64-year-old female patient was presented to the hospital due to low back pain. She was diagnosed with postmenopausal osteoporosis based on bone density scan score and a compression fracture of the L1 vertebral body revealed by X-ray. She was treated with a weekly bisphosphonate and supplementation with vitamin D and calcium. After one year, monthly bisphosphonate was introduced in therapy because of an inadequate response. In April 2020, the patient was treated for COVID-19 according to protocol, and during the treatment, bisphosphonate therapy was discontinued. After five months, she suffered a fracture of her left forearm. Due to the persistence of low mineral bone density, which was complicated by a new fracture, denosumab 60 mg subcutaneously once every six months was initiated with additional vitamin D and calcium supplementation. At six months follow-up, an increase in mineral bone density was verified, and after 12 months, the dual-energy x-ray absorptiometry score was within the osteopenia range. Laboratory findings showed a decrease in bone turnover markers. Conclusion. One-year administration of denosumab led to a significant increase in bone mineral density measured at the lumbar spine and neck of the femur, as well as changes in the levels of biochemical markers of bone synthesis and resorption, and reduced the risk of new fractures.
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骨质疏松症的生物治疗-解决临床问题- 1例报告
介绍。骨质疏松症的发病机制的阐明促进了生物制剂类新药的开发。病例报告。2018年4月,一名64岁女性患者因腰痛就诊。根据骨密度扫描评分和x线显示L1椎体压缩性骨折,诊断为绝经后骨质疏松症。患者每周服用双膦酸盐并补充维生素D和钙。一年后,由于反应不足,每月引入双膦酸盐治疗。2020年4月,患者按照方案接受新冠肺炎治疗,治疗期间停用双膦酸盐治疗。五个月后,她的左前臂骨折。由于持续的低矿物质骨密度,并伴有新的骨折,每六个月一次皮下注射denosumab 60mg,同时补充维生素D和钙。随访6个月,证实矿物质骨密度增加,12个月后,双能x线骨密度评分在骨质减少范围内。实验室结果显示骨转换标志物减少。结论。给药1年的denosumab导致腰椎和股骨颈骨矿物质密度显著增加,骨合成和骨吸收生化标志物水平发生变化,并降低了新骨折的风险。
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