Department of Nephrology, The Affiliated Hospital of Qingdao University Medical College, No. 16 Jiangsu Road, The Southern Direct, Qingdao City, Shandong Province, China.
Endocrine. 2013 Feb;43(1):68-77. doi: 10.1007/s12020-012-9711-2. Epub 2012 Jun 6.
Cinacalcet, the first calcimimetic to be approved for the treatment of secondary hyperparathyroidism (SHPT) in the chronic kidney disease patients, offers a novel therapeutic approach to SHPT. The aim of this meta-analysis is to access the efficacy and safety of cinacalcet on bone and mineral metabolism disorders in the dialysis patients with SHPT. Randomized controlled trials on cinacalcet combined with vitamin D and/or phosphate binders in the dialysis patients with SHPT were identified in Pubmed, Sciencedirect, and the Cochrane library. Data were analyzed with RevMan software. We compared the proportion of patients achieving the biochemical targets recommended by the Kidney Disease Outcomes Quality Initiative (KDOQI) guidelines and the incidence of adverse events between the cinacalcet and control groups. Six trials involving 2,548 patients were included. A greater proportion of patients in the cinacalcet group compared with the conventional group achieved the KDOQI targets. The relative risks (RRs) were parathyroid hormone (PTH) (RR = 3.51, 95 % CI: 2.38-5.17), calcium (RR = 2.04, 95 % CI: 1.76-2.37), phosphorus (RR = 1.15, 95 % CI: 0.83-1.60), and calcium-phosphorus product (Ca × P) (RR = 1.41, 95 % CI: 1.18-1.69), the number of patients simultaneously achieving the KDOQI targets for PTH + Ca × P was also greater (RR = 3.89, 95 % CI: 2.36-6.41), with p < 0.001 for each. The most common adverse events were nausea, vomiting, diarrhea, and hypocalcemia, which had a higher incidence in the cinacalcet group, but were usually mild to moderate in severity and transient. Compared with conventional therapy, treatment with cinacalcet results in more patients achieving KDOQI targets and offers an effective and safety therapeutic option for controlling mineral and bone disorders in the dialysis patients with SHPT.
西那卡塞是首个被批准用于治疗慢性肾脏病患者继发性甲状旁腺功能亢进症 (SHPT) 的拟钙剂,为 SHPT 提供了一种新的治疗方法。本荟萃分析旨在评估西那卡塞治疗透析患者 SHPT 时对骨骼和矿物质代谢紊乱的疗效和安全性。在 Pubmed、Sciencedirect 和 Cochrane 图书馆中检索到西那卡塞联合维生素 D 和/或磷结合剂治疗透析患者 SHPT 的随机对照试验。使用 RevMan 软件对数据进行分析。我们比较了西那卡塞组和对照组达到肾脏病预后质量倡议 (KDOQI) 指南推荐的生化目标的患者比例和不良事件的发生率。纳入了 6 项涉及 2548 名患者的试验。与常规组相比,西那卡塞组有更多的患者达到 KDOQI 目标。相对风险 (RR) 分别为甲状旁腺激素 (PTH) (RR = 3.51,95 % CI:2.38-5.17)、钙 (RR = 2.04,95 % CI:1.76-2.37)、磷 (RR = 1.15,95 % CI:0.83-1.60) 和钙磷乘积 (Ca × P) (RR = 1.41,95 % CI:1.18-1.69),同时达到 KDOQI 推荐的 PTH + Ca × P 目标的患者数量也更多 (RR = 3.89,95 % CI:2.36-6.41),p < 0.001。最常见的不良反应为恶心、呕吐、腹泻和低钙血症,西那卡塞组的发生率较高,但通常为轻度至中度且短暂。与常规治疗相比,西那卡塞治疗可使更多的患者达到 KDOQI 目标,为控制透析患者 SHPT 时的矿物质和骨骼紊乱提供了一种有效且安全的治疗选择。