CliCon S.r.l. Health, Economics & Outcomes Research, Bologna, Italy.
UOC Assistenza Farmaceutica Territoriale, Azienda ULSS 8 Berica, Vicenza, Italy.
J Bone Miner Res. 2021 Nov;36(11):2177-2183. doi: 10.1002/jbmr.4419. Epub 2021 Aug 22.
The determinants of the susceptibility to severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection and severe coronavirus disease 2019 (COVID-19) manifestations are yet not fully understood. Amino-bisphosphonates (N-BPs) have anti-inflammatory properties and have been shown to reduce the incidence of lower respiratory infections, cardiovascular events, and cancer. We conducted a population-based retrospective observational cohort study with the primary objective of determining if oral N-BPs treatment can play a role in the susceptibility to development of severe COVID-19. Administrative International Classification of Diseases, Ninth Revision, Clinical ModificationI (ICD-9-CM) and anatomical-therapeutic chemical (ATC) code data, representative of Italian population (9% sample of the overall population), were analyzed. Oral N-BPs (mainly alendronate and risedronate) were included in the analysis, zoledronic acid was excluded because of the low number of patients at risk. Incidence of COVID-19 hospitalization was 12.32 (95% confidence interval [CI], 9.61-15.04) and 11.55 (95% CI, 8.91-14.20), of intensive care unit (ICU) utilization because of COVID-19 was 1.25 (95% CI, 0.38-2.11) and 1.42 (95% CI, 0.49-2.36), and of all-cause death was 4.06 (95% CI, 2.50-5.61) and 3.96 (95% CI, 2.41-5.51) for oral N-BPs users and nonusers, respectively. Sensitivity analyses that excluded patients with prevalent vertebral or hip fragility fractures and without concomitant glucocorticoid treatment yielded similar results. In conclusion, we found that the incidence of COVID-19 hospitalization, intensive care unit (ICU) utilization, and COVID-19 potentially related mortality were similar in N-BPs-treated and nontreated subjects. Similar results were found in N-BPs versus other anti-osteoporotic drugs. We provide real-life data on the safety of oral N-BPs in terms of severe COVID-19 risk on a population-based cohort. Our results do not support the hypothesis that oral N-BPs can prevent COVID-19 infection and/or severe COVID-19; however, they do not seem to increase the risk. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染和 2019 年冠状病毒病(COVID-19)严重表现的易感性的决定因素尚不完全清楚。氨基双膦酸盐(N-BPs)具有抗炎特性,已被证明可降低下呼吸道感染、心血管事件和癌症的发生率。我们进行了一项基于人群的回顾性观察性队列研究,主要目的是确定口服 N-BPs 治疗是否可以降低发展为严重 COVID-19 的易感性。分析了行政国际疾病分类,第九修订版,临床修正(ICD-9-CM)和解剖治疗化学(ATC)代码数据,代表意大利人群(总体人群的 9%样本)。分析中包括口服 N-BPs(主要是阿仑膦酸盐和利塞膦酸盐),排除了唑来膦酸,因为风险患者数量较少。COVID-19 住院的发生率为 12.32(95%置信区间[CI],9.61-15.04)和 11.55(95%CI,8.91-14.20),因 COVID-19 而入住重症监护病房(ICU)的发生率为 1.25(95%CI,0.38-2.11)和 1.42(95%CI,0.49-2.36),全因死亡率为 4.06(95%CI,2.50-5.61)和 3.96(95%CI,2.41-5.51),分别为口服 N-BPs 使用者和非使用者。排除有既往椎体或髋部脆性骨折且无同时使用糖皮质激素治疗的患者的敏感性分析得出了类似的结果。总之,我们发现 COVID-19 住院、重症监护病房(ICU)使用和 COVID-19 相关死亡的发生率在 N-BPs 治疗和未治疗的患者中相似。在 N-BPs 与其他抗骨质疏松药物的比较中也发现了类似的结果。我们基于人群队列提供了关于口服 N-BPs 在严重 COVID-19 风险方面安全性的真实数据。我们的结果不支持口服 N-BPs 可预防 COVID-19 感染和/或严重 COVID-19 的假设;然而,它们似乎并没有增加风险。2021 年,作者。《骨与矿物研究杂志》由 Wiley 期刊出版公司代表美国骨与矿物研究协会(ASBMR)出版。