Nishimoto Masatoshi, Hasegawa Takeshi, Murashima Miho, Noma Hisashi, Nishiwaki Hiroki, Yamada Shunsuke, Mizukami Aya, Saito Hirotaka, Kimura Hiroshi, Taniguchi Masatomo, Hamano Takayuki, Fukagawa Masafumi
Department of Nephrology, Nara Medical University, Nara, Japan.
Institute of Clinical Epidemiology (iCE), Showa Medical University, Tokyo, Japan.
Clin J Am Soc Nephrol. 2025 May 1;20(5):676-696. doi: 10.2215/CJN.0000000665. Epub 2025 Mar 14.
Sevelamer was associated with lower all-cause mortality compared with calcium-based agents. Sucroferric oxyhydroxide and tenapanor were estimated to rank high in lowering all-cause mortality compared with other phosphate-lowering agents. Sucroferric oxyhydroxide and lanthanum were associated with slower progression of coronary artery calcium score compared with calcium-based agents.
It is necessary to update the evidence of each phosphate-lowering agent on dialysis patients.
From the CENTRAL, MEDLINE, Embase, and ClinicalTrial.gov databases, randomized controlled trials using oral phosphate-lowering agents on adult patients requiring maintenance dialysis were extracted. The treatment period was required for 8 or more weeks, and the risk of bias was assessed according to the Cochrane Collaboration method. The outcomes were all-cause mortality, cardiovascular mortality, gastrointestinal events, fracture, coronary artery calcium score (CACS), serum calcium, phosphate, intact parathyroid hormone, and bicarbonate levels. A network meta-analyses using multivariate random-effects models were performed for assessing the comparative effectiveness. The ranking of the phosphate-lowering agents was assessed using a surface under the cumulative ranking curve.
A total of 70 randomized controlled trials involving 15,551 participants were included. Eleven phosphate-lowering agents including calcium-based agents, sevelamer, bixalomer, lanthanum, sucroferric oxyhydroxide, ferric citrate, tenapanor, magnesium, nicotinamide, aluminum, and sucralfate were assessed. Sevelamer was significantly associated with lower all-cause mortality compared with calcium-based agents (risk ratio [95% confidence interval]: 0.59 [0.37 to 0.94]), and sucroferric oxyhydroxide and tenapanor were estimated to rank high in lowering all-cause mortality on the basis of the surface under the cumulative ranking curve. The risk of gastrointestinal events was the highest with nicotinamide, followed by sucroferric oxyhydroxide. Compared with calcium-based agents, CACS was significantly lower among those on lanthanum and sucroferric oxyhydroxide (standardized mean difference [95% confidence interval]: −0.26 [−0.52 to −0.01] and −0.50 [−0.95 to−0.06], respectively). Serum calcium levels were higher, and serum intact parathyroid hormone levels were lower in patients treated with calcium-based agents. Except for sevelamer, serum bicarbonate levels for all other agents were higher compared with placebo.
Compared with calcium-based agents, sevelamer was associated with lower all-cause mortality, and sucroferric oxyhydroxide and lanthanum were associated with slower progression of CACS. Potential benefits and harms should be considered when selecting phosphate-lowering agents (International prospective register of systematic reviews: CRD42022328388).
与钙基药物相比,司维拉姆与全因死亡率较低相关。与其他降磷药物相比,羟基氧化蔗糖铁和替那帕诺在降低全因死亡率方面估计排名靠前。与钙基药物相比,羟基氧化蔗糖铁和镧与冠状动脉钙化评分进展较慢相关。
有必要更新每种降磷药物对透析患者的证据。
从CENTRAL、MEDLINE、Embase和ClinicalTrial.gov数据库中,提取对需要维持透析的成年患者使用口服降磷药物的随机对照试验。治疗期要求为8周或更长时间,并根据Cochrane协作方法评估偏倚风险。结局指标为全因死亡率、心血管死亡率、胃肠道事件、骨折、冠状动脉钙化评分(CACS)、血清钙、磷、完整甲状旁腺激素和碳酸氢盐水平。使用多变量随机效应模型进行网络荟萃分析以评估比较疗效。使用累积排名曲线下的面积评估降磷药物的排名。
共纳入70项涉及15551名参与者的随机对照试验。评估了11种降磷药物,包括钙基药物、司维拉姆、比沙洛美、镧、羟基氧化蔗糖铁、柠檬酸铁、替那帕诺、镁、烟酰胺、铝和硫糖铝。与钙基药物相比,司维拉姆与较低的全因死亡率显著相关(风险比[95%置信区间]:0.59[0.37至0.94]),并且根据累积排名曲线下的面积,羟基氧化蔗糖铁和替那帕诺在降低全因死亡率方面估计排名靠前。烟酰胺的胃肠道事件风险最高,其次是羟基氧化蔗糖铁。与钙基药物相比,服用镧和羟基氧化蔗糖铁的患者的CACS显著更低(标准化均值差[95%置信区间]:分别为−0.26[−0.52至−0.01]和−0.50[−0.95至−0.06])。接受钙基药物治疗的患者血清钙水平较高,血清完整甲状旁腺激素水平较低。除司维拉姆外,所有其他药物的血清碳酸氢盐水平与安慰剂相比更高。
与钙基药物相比,司维拉姆与较低的全因死亡率相关,羟基氧化蔗糖铁和镧与CACS进展较慢相关。选择降磷药物时应考虑潜在的益处和危害(国际系统评价前瞻性注册库:CRD42022328388)。