ICES, Toronto, Canada.
Department of Medicine, Western University, London, Canada.
J Bone Miner Res. 2023 May;38(5):650-658. doi: 10.1002/jbmr.4804. Epub 2023 Apr 9.
Denosumab can be used in patients with chronic kidney disease (CKD) but has been linked with cases of severe hypocalcemia. The incidence of and risk factors for hypocalcemia after denosumab use are not well established. Using linked health care databases at ICES, we conducted a population-based cohort study of adults >65 years old with a new prescription for denosumab or a bisphosphonate between 2012 and 2020. We assessed incidence of hypocalcemia within 180 days of drug dispensing and stratified results by estimated glomerular filtration rate (eGFR in mL/min/1.73 m ). We used Cox proportional hazards to assess risk factors for hypocalcemia. There were 59,151 and 56,847 new denosumab and oral bisphosphonate users, respectively. Of the denosumab users, 29% had serum calcium measured in the year before their prescription, and one-third had their serum calcium checked within 180 days after their prescription. Mild hypocalcemia (albumin corrected calcium <2.00 mmol/L) occurred in 0.6% (95% confidence interval [CI] 0.6, 0.7) of new denosumab users and severe hypocalcemia (<1.8 mmol/L) in 0.2% (95% CI 0.2, 0.3). In those with an eGFR <15 or receiving maintenance dialysis, the incidence of mild and severe hypocalcemia was 24.1% (95% CI 18.1, 30.7) and 14.9% (95% CI 10.1, 20.7), respectively. In this group, kidney function and baseline serum calcium were strong predictors of hypocalcemia. We did not have information on over-the-counter vitamin D or calcium supplementation. In new bisphosphonate users, the incidence of mild hypocalcemia was 0.3% (95% CI 0.3, 0.3) with an incidence of 4.7% (95% CI 1.5, 10.8) in those with an eGFR <15 or receiving maintenance dialysis. In this large population-based cohort, we found that the overall risk of hypocalcemia with new denosumab use was low but increased substantially in those with eGFR <15 mL/min/1.73 m . Future studies should investigate strategies to mitigate hypocalcemia. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
地舒单抗可用于慢性肾脏病(CKD)患者,但与严重低钙血症有关。地舒单抗使用后低钙血症的发生率和危险因素尚未确定。我们使用安大略省癌症研究所(ICES)的链接医疗保健数据库,对 2012 年至 2020 年间新开具地舒单抗或双膦酸盐处方的>65 岁成年人进行了一项基于人群的队列研究。我们评估了药物配药后 180 天内低钙血症的发生率,并按估计肾小球滤过率(eGFR,以 mL/min/1.73 m 表示)分层结果。我们使用 Cox 比例风险评估低钙血症的危险因素。新使用地舒单抗和口服双膦酸盐的患者分别为 59151 例和 56847 例。在使用地舒单抗的患者中,29%的患者在处方前一年检测了血清钙,三分之一的患者在处方后 180 天内检查了血清钙。新使用地舒单抗的患者中有 0.6%(95%置信区间 [CI],0.6,0.7)发生轻度低钙血症(白蛋白校正钙<2.00 mmol/L),0.2%(95%CI,0.2,0.3)发生严重低钙血症(<1.8 mmol/L)。在 eGFR<15 或接受维持性透析的患者中,轻度和重度低钙血症的发生率分别为 24.1%(95%CI,18.1,30.7)和 14.9%(95%CI,10.1,20.7)。在这组患者中,肾功能和基线血清钙是低钙血症的强烈预测因素。我们没有关于非处方维生素 D 或钙补充剂的信息。在新使用双膦酸盐的患者中,轻度低钙血症的发生率为 0.3%(95%CI,0.3,0.3),eGFR<15 或接受维持性透析的患者发生率为 4.7%(95%CI,1.5,10.8)。在这项大型基于人群的队列研究中,我们发现新使用地舒单抗后低钙血症的总体风险较低,但 eGFR<15 mL/min/1.73 m 的患者风险显著增加。未来的研究应探讨降低低钙血症风险的策略。