Anti-osteoporotic treatment and COVID-19 risk: is there an association?

N. Grygorieva, M. Bystrytska, N. Zaverukha, A. Musiienko
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Abstract

Introduction. Despite the recent ASBMR, AACE, Endocrine Society, ECTS&NOF guidelines for osteoporosis management in the era of COVID-19 the impact of antiosteoporotic drugs on disease risk and severity is insufficiently studied. The purpose of this study was to assess the COVID-19 risk for the patients receiving the parenteral bisphosphonate or Denosumab treatment, and the severity of its course in patients with systemic osteoporosis. Materials and methods. We performed the phone survey and studied the results of 195 patients (92 % women; mean age – 62.7 ± 10.8 years) with systemic osteoporosis depending on the current use of parenteral antiresorptive drugs (Zoledronic, Ibandronic acids, or Denosumab, n = 125) and compared the results with data of the patients with osteoporosis who did not use any anti-osteoporotic drugs previously (n = 70). Results. The group of patients with COVID-19 included 32.9 % of patients who did not receive previously any anti-osteoporotic treatment and 33.3 % of osteoporotic patients treated with parenteral antiresorptive drugs. The share of the patients taking the Zoledronic acid who fell ill with COVID-19 was 29.2 %, the share of those ta­king the Ibandronic acid was 34.4 %, and the share of those taking Denosumab was 42.9 %. We did not reveal any significant differences in the COVID-19 frequency and severity depending on the presence and type of parenteral anti-osteoporotic therapy. Additionally, there were no differences depen­ding on the patients' age, gender, obesity, and other osteoporosis risk factors. The risk of COVID-19 in the patients with systemic osteoporosis did not differ depending on antiresorptive drug use, amounting (odds ratio (OR) 95 % CI) 1.1 (0.6-2.0), or on the use of the definite anti-osteoporotic drug (for the Zoledronic acid – 0.9 (0.4-2.0), the Ibandronic acid – 1.1 (0.5-2.3), and for the Denosumab – 1.6 (0.5-5.2). Conclusions. Parenteral anti-osteoporo­tic drugs (Zoledronic acid, Ibandronic acid, or Denosumab) do not have any influence on COVID-19 frequency and severity and can be recommended for the continuation of the treatment of patients with osteoporosis.
抗骨质疏松治疗与COVID-19风险:是否存在关联?
介绍。尽管最近ASBMR、AACE、内分泌学会、ects和nof等针对COVID-19时代骨质疏松症的管理指南,但抗骨质疏松药物对疾病风险和严重程度的影响研究不足。本研究的目的是评估接受肠外双膦酸盐或Denosumab治疗的患者发生COVID-19的风险,以及系统性骨质疏松患者的病程严重程度。材料和方法。我们进行了电话调查,研究了195名患者的结果(92%为女性;平均年龄- 62.7±10.8岁),根据目前使用的肠外抗骨质吸收药物(唑来膦酸、依邦膦酸或Denosumab, n = 125),并将结果与以前未使用任何抗骨质疏松药物的骨质疏松症患者的数据(n = 70)进行比较。结果。在COVID-19患者组中,32.9%的患者以前没有接受过任何抗骨质疏松治疗,33.3%的骨质疏松患者接受过肠外抗吸收药物治疗。服用唑来膦酸的患者感染新冠肺炎的比例为29.2%,服用依邦膦酸的比例为34.4%,服用Denosumab的比例为42.9%。我们没有发现根据肠外抗骨质疏松治疗的存在和类型,COVID-19的频率和严重程度有任何显著差异。此外,患者的年龄、性别、肥胖和其他骨质疏松危险因素没有差异。在系统性骨质疏松患者中,COVID-19的风险并不取决于抗吸收药物的使用(优势比(OR) 95% CI)为1.1(0.6-2.0),或使用明确的抗骨质疏松药物(唑来膦酸为0.9(0.4-2.0),依邦膦酸为1.1 (0.5-2.3),Denosumab为1.6(0.5-5.2))。结论。静脉注射抗骨质疏松药物(唑来膦酸、依邦膦酸或地诺单抗)对COVID-19的发生频率和严重程度没有任何影响,可推荐用于骨质疏松患者的继续治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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