Endocrinology and Diabetes Unit, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Department of Medicine and Surgery, University of Milano Bicocca, Milan, Italy.
Front Endocrinol (Lausanne). 2023 Dec 7;14:1283101. doi: 10.3389/fendo.2023.1283101. eCollection 2023.
Denosumab is a monoclonal antibody blocking the receptor activator of nuclear factor kappa-B/receptor activator of nuclear factor kappa-B ligand (RANK/RANKL) pathway, thus inhibiting osteoclastogenesis. Since RANK and RANKL are also involved in the immune system activation, denosumab might interfere with the response against infections. Our study aimed to explore the relationship between denosumab treatment and coronavirus disease 2019 (COVID-19).
The occurrence and severity of COVID-19 were recorded in consecutive patients referred to the Endocrinology Department of Papa Giovanni XXIII Hospital, Bergamo, from 1 January 2020 to 1 January 2021. Patients treated with denosumab were compared to outpatient controls. Patients' features were summarized by descriptive statistics. Multivariate logistic regression assessed the relationship between denosumab and COVID-19, adjusting for potential confounders. Subgroup analyses according to age, sex, body mass index (BMI), smoking status, and vitamin D levels were performed.
The final population included 331 patients treated with denosumab and 357 controls. COVID-19 incidence was lower in the denosumab group (7.6% vs. 14.6%, p = 0.004). COVID-19 severity was similar in both groups. Multiple logistic regression confirmed an association between denosumab and a reduced occurrence of symptomatic COVID-19 [odds ratio (OR) 0.46, 95% CI 0.21-0.98, p = 0.049]. Subgroup analyses suggested a potential protective effect of denosumab in patients over 75 years (OR 0.12, 95% CI 0.02-0.6, p = 0.011), with a significant interaction between denosumab and age categories (p = 0.047).
Our study confirms that denosumab may be safely continued in COVID-19 patients. RANK/RANKL inhibition seems associated with a reduced incidence of symptomatic COVID-19, particularly among the elderly.
地舒单抗是一种单克隆抗体,可阻断核因子κ B 受体激活剂/核因子κ B 受体激活剂配体(RANK/RANKL)通路的受体,从而抑制破骨细胞生成。由于 RANK 和 RANKL 也参与免疫系统的激活,地舒单抗可能会干扰对感染的反应。我们的研究旨在探讨地舒单抗治疗与 2019 年冠状病毒病(COVID-19)之间的关系。
连续记录了 2020 年 1 月 1 日至 2021 年 1 月 1 日期间被转诊到贝加莫 Papa Giovanni XXIII 医院内分泌科的患者中 COVID-19 的发生和严重程度。将接受地舒单抗治疗的患者与门诊对照患者进行比较。通过描述性统计总结患者的特征。多变量逻辑回归评估了地舒单抗与 COVID-19 之间的关系,并调整了潜在混杂因素。根据年龄、性别、体重指数(BMI)、吸烟状况和维生素 D 水平进行亚组分析。
最终人群包括 331 名接受地舒单抗治疗的患者和 357 名对照患者。地舒单抗组 COVID-19 的发生率较低(7.6%比 14.6%,p=0.004)。两组 COVID-19 的严重程度相似。多变量逻辑回归证实,地舒单抗与症状性 COVID-19 的发生减少相关[比值比(OR)0.46,95%可信区间(CI)0.21-0.98,p=0.049]。亚组分析提示地舒单抗在 75 岁以上患者中可能具有潜在的保护作用(OR 0.12,95%CI 0.02-0.6,p=0.011),地舒单抗与年龄类别之间存在显著交互作用(p=0.047)。
我们的研究证实,COVID-19 患者可安全继续接受地舒单抗治疗。RANK/RANKL 抑制似乎与症状性 COVID-19 的发生率降低相关,特别是在老年人中。