Dave Vatsa, Chiang Cherie Y, Booth Jane, Mount Peter F
Department of Nephrology, Austin Health, Heidelberg, Melbourne, Vic., Australia.
Am J Nephrol. 2015;41(2):129-37. doi: 10.1159/000380960. Epub 2015 Mar 18.
Denosumab, a RANK-ligand inhibitor, is an effective treatment for osteoporosis in postmenopausal women and men. Unlike the bisphosphonates, it is not excreted by the kidney. Little is known, however, about its efficacy and safety in patients with severe chronic kidney disease (CKD).
A retrospective study was performed in CKD 4-5D patients from a tertiary referral hospital who were treated with denosumab between 1st January 2011 and 31st March 2014. Data collected included information about the following: CKD stage, fracture history, bone mineral density, serum calcium levels pre and post denosumab treatment, episodes of hypocalcemia, relevant medications and adverse events.
Eight patients with CKD-5 and 6 patients with CKD-4 were identified (all female, mean age 77.1 ± 9.9). The mean pre-denosumab calcium value was 2.42 ± 0.12 mmol/l, PTH 20.2 ± 14.7 pmol/l and 25-OH vitamin D 69.1 ± 30.1 nmol/l. After denosumab treatment, 6/8 patients with CKD-5/5D, and 2/5 patients with CKD-4 developed severe hypocalcemia. Two patients developed direct adverse complications of hypocalcemia (seizure, laryngospasm, prolonged QTc). Among the patients who developed hypocalcemia, the median time to serum calcium nadir was 21 days and the median time to correction of hypocalcemia was 71 days. Treatment of hypocalcemia required large doses of oral calcium and calcitriol, and increases in dialysate calcium concentration.
A high rate of severe hypocalcemia was observed in patients with advanced CKD treated with denosumab. If denosumab is used in patients with severe CKD, close monitoring and aggressive replacement of calcium and calcitriol is required to avoid the development of hypocalcemia.
地诺单抗是一种核因子κB受体活化因子配体(RANK-ligand)抑制剂,是绝经后女性和男性骨质疏松症的有效治疗药物。与双膦酸盐不同,它不由肾脏排泄。然而,对于严重慢性肾脏病(CKD)患者,其疗效和安全性知之甚少。
对一家三级转诊医院2011年1月1日至2014年3月31日期间接受地诺单抗治疗的CKD 4-5D期患者进行回顾性研究。收集的数据包括以下信息:CKD分期、骨折史、骨密度、地诺单抗治疗前后的血清钙水平、低钙血症发作情况、相关药物及不良事件。
共纳入8例CKD-5期患者和6例CKD-4期患者(均为女性,平均年龄77.1±9.9岁)。地诺单抗治疗前的平均钙值为2.42±0.12 mmol/l,甲状旁腺激素(PTH)为20.2±14.7 pmol/l,25-羟维生素D为69.1±30.1 nmol/l。地诺单抗治疗后,8例CKD-5/5D期患者中的6例以及5例CKD-4期患者中的2例发生了严重低钙血症。2例患者出现了低钙血症的直接不良并发症(癫痫、喉痉挛、QTc延长)。在发生低钙血症的患者中,血清钙最低点的中位时间为21天,低钙血症纠正的中位时间为71天。低钙血症的治疗需要大剂量口服钙剂和骨化三醇,并提高透析液钙浓度。
接受地诺单抗治疗的晚期CKD患者中观察到高比例的严重低钙血症。如果在严重CKD患者中使用地诺单抗,需要密切监测并积极补充钙剂和骨化三醇,以避免发生低钙血症。