Institute of Endocrinology, Diabetes and Metabolism, Rabin Medical Center - Beilinson Hospital, 39 Jabotinski St., 4941492, Petah Tikva, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Osteoporos Int. 2020 Apr;31(4):655-665. doi: 10.1007/s00198-019-05261-7. Epub 2019 Dec 14.
Hypocalcemia was reported at low rates (0.05-1.7%) in denosumab-treated postmenopausal women with osteoporosis. This real-life study shows a 7.4% rate of denosumab-induced hypocalcemia in community-dwelling osteoporotic men and women. Pretreatment serum calcium and creatinine levels are major predictors for this complication. Serum-calcium monitoring may help to identify and prevent severe hypocalcemia.
RCTs have reported a 0.05-1.7% rate of hypocalcemia in denosumab-treated postmenopausal women with osteoporosis, but long-term real-life data are lacking. We assessed the rate of hypocalcemia in osteoporotic community-dwelling patients treated with denosumab.
A retrospective analysis was conducted based on medical records (2010-2018) from a large HMO. An albumin-adjusted serum calcium concentration lower than 8.5 mg/dL was defined as hypocalcemia.
We included 2005 patients (93% women, mean age 76 ± 9 years). Hypocalcemia developed during treatment in 149 patients (7.4%; 1% less than 8 mg/dL): in 66 after 0.5-1 years; 48 after 1-2 years; 35 after > 2 years. On comparison of the hypocalcemic and normocalcemic patients, the strongest predictors of hypocalcemia were pretreatment levels of albumin-adjusted serum calcium (9.1 ± 0.4 vs. 9.4 ± 0.5 mg/dL, respectively; p < 0.05) and creatinine (0.9 ± 0.5 vs. 0.8 ± 0.3 mg/dL, respectively; p < 0.05). The hypocalcemia rate increased in parallel to a decrease in eGFR (p = 0.032 for the difference between eGFR ranges). Baseline calcium level ≤ 9.31 mg/dL predicted hypocalcemia with a sensitivity of 77% and specificity of 56%. A model of (- 2)*calcium + creatinine predicted hypocalcemia (3.7% when lower and 17.1% when higher than - 17.4). Gender, age, 25-hydroxyvitamin-D, parathyroid hormone, alkaline phosphatase, and whether denosumab was given as first or advanced line of osteoporotic therapy had no predictive value.
Real-life rates of denosumab-induced hypocalcemia are higher than previously reported. Hypocalcemia might develop after each dose of denosumab in ongoing treatment. Adequate calcium and vitamin D supplementation are needed. Serum calcium monitoring is advised in high-risk patients for early detection of severe hypocalcemia.
RCT 报道了接受地舒单抗治疗的绝经后骨质疏松症女性中低钙血症的发生率为 0.05-1.7%,但缺乏长期真实世界的数据。我们评估了地舒单抗治疗的社区居住骨质疏松症患者中低钙血症的发生率。
对来自大型 HMO 的病历(2010-2018 年)进行回顾性分析。白蛋白校正血清钙浓度低于 8.5mg/dL 定义为低钙血症。
共纳入 2005 例患者(93%为女性,平均年龄 76±9 岁)。149 例(7.4%;1%低于 8mg/dL)在治疗期间发生低钙血症:66 例发生在 0.5-1 年后;48 例发生在 1-2 年后;35 例发生在>2 年后。在比较低钙血症和血钙正常患者时,低钙血症的最强预测因素是治疗前白蛋白校正血清钙水平(分别为 9.1±0.4mg/dL 和 9.4±0.5mg/dL;p<0.05)和肌酐水平(分别为 0.9±0.5mg/dL 和 0.8±0.3mg/dL;p<0.05)。低钙血症发生率与 eGFR 降低呈平行关系(eGFR 范围之间的差异 p=0.032)。基线血钙水平≤9.31mg/dL 预测低钙血症的敏感性为 77%,特异性为 56%。钙水平-2*肌酐预测低钙血症(低值时为 3.7%,高值时为 17.1%)。性别、年龄、25-羟维生素 D、甲状旁腺激素、碱性磷酸酶以及地舒单抗是否作为骨质疏松症的一线或二线治疗药物均无预测价值。
地舒单抗引起的低钙血症的真实世界发生率高于既往报道。在持续治疗中,每次给予地舒单抗后可能会发生低钙血症。需要充足的钙和维生素 D 补充。建议高危患者进行血钙监测,以便早期发现严重低钙血症。