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一种用于识别绝经后骨质疏松症患者中接受地舒单抗治疗后低钙血症高风险人群的简易评分:一项真实世界队列研究。

A Simple-to-Use Score for Identifying Individuals at High Risk of Denosumab-Associated Hypocalcemia in Postmenopausal Osteoporosis: A Real-World Cohort Study.

机构信息

Department of Internal Medicine, Severance Hospital, Endocrine Research Institute, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.

Department of Internal Medicine, Korea University College of Medicine, Seoul, Republic of Korea.

出版信息

Calcif Tissue Int. 2020 Dec;107(6):567-575. doi: 10.1007/s00223-020-00754-8. Epub 2020 Sep 12.

Abstract

Since denosumab-associated hypocalcemia occurs infrequently, data on its incidence and risk factors are limited. We aimed to evaluate risk factors and develop a useful score for identifying individuals at risk of denosumab-associated hypocalcemia. In this retrospective cohort, 790 consecutive female patients who received 60 mg denosumab at least once between 2016 and 2017 were analyzed. Based on biochemical records from a large-scale single-center, mild and moderate hypocalcemia were defined as albumin-corrected calcium (cCa) levels < 8.5 and < 8.0 mg/dL (< 2.12 and < 2.0 mmol/L), respectively. Mild and moderate hypocalcemia were observed in 8.2% and 1.0% patients, respectively. Patients who developed mild hypocalcemia had lower baseline cCa (8.9 vs. 9.3 mg/dL and 2.22 vs. 2.32mmo/L) and estimated glomerular filtration rate (75.0 vs. 83.2 mL/min/1.73 m) and more frequent loop diuretic use (10.8% vs. 4.4%; all p < 0.05). In multivariate analysis, low baseline cCa (OR 1.29; 95% CI 1.20-1.40) and chronic kidney disease (CKD) stages 3b-5 were associated with elevated mild hypocalcemia risk (OR 2.92; 95% CI 1.38-6.20). Loop diuretics use was associated with mild hypocalcemia (OR 2.61; 95% CI 1.11-6.18) by univariate analysis, independent of baseline cCa and CKD stage. A scoring approach identified two risk groups: (1) patients without CKD (eGFR ≥ 45) and cCa < 8.5 mg/dL (2.12 mmol/L) and (2) patients with CKD (eGFR < 45) and cCa < 9.5 mg/dL (2.37 mmol/L).

摘要

由于地舒单抗相关性低钙血症的发生率较低,因此其发病机制和危险因素的数据有限。我们旨在评估危险因素,并建立一个有用的评分系统来识别地舒单抗相关性低钙血症的高危人群。在这项回顾性队列研究中,分析了 2016 年至 2017 年期间至少接受过 60mg 地舒单抗治疗的 790 例连续女性患者。根据来自大型单中心的生化记录,轻度和中度低钙血症定义为白蛋白校正钙(cCa)水平<8.5mg/dL(<2.12mmol/L)和<8.0mg/dL(<2.0mmol/L)。分别有 8.2%和 1.0%的患者出现轻度和中度低钙血症。发生轻度低钙血症的患者基线 cCa 较低(8.9mg/dL 比 9.3mg/dL 和 2.22mmol/L 比 2.32mmol/L),估算肾小球滤过率(75.0mL/min/1.73m 比 83.2mL/min/1.73m)和更频繁使用袢利尿剂(10.8%比 4.4%;均 P<0.05)。多因素分析显示,基线 cCa 较低(比值比 1.29;95%可信区间 1.20-1.40)和慢性肾脏病(CKD)3b-5 期与轻度低钙血症风险升高相关(比值比 2.92;95%可信区间 1.38-6.20)。单因素分析显示,袢利尿剂的使用与轻度低钙血症相关(比值比 2.61;95%可信区间 1.11-6.18),而与基线 cCa 和 CKD 分期无关。一种评分方法确定了两个风险组:(1)无 CKD(eGFR≥45)和 cCa<8.5mg/dL(2.12mmol/L)的患者;(2)有 CKD(eGFR<45)和 cCa<9.5mg/dL(2.37mmol/L)的患者。

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