Habbous Steven, Przech Sebastian, Acedillo Rey, Sarma Sisira, Garg Amit X, Martin Janet
Department of Epidemiology & Biostatistics, Western University, London, ON, Canada.
London Health Sciences Centre, Division of Nephrology, Western University, London, ON, Canada.
Nephrol Dial Transplant. 2017 Jan 1;32(1):111-125. doi: 10.1093/ndt/gfw312.
It remains unclear which phosphate binders should be preferred for hyperphosphatemia management in chronic kidney disease (CKD).
We performed a systematic review and meta-analysis of randomized trials comparing sevelamer or lanthanum with other phosphate binders in CKD.
Fifty-one trials (8829 patients) were reviewed. Compared with calcium-based binders, all-cause mortality was nonsignificantly lower with sevelamer {risk ratio [RR] 0.62 [95% confidence interval (CI) 0.35-1.08]} and lanthanum [RR 0.73 (95% CI 0.18-3.00)], but risk of bias was concerning. Compared with calcium-based binders, sevelamer reduced the risk of hypercalcemia [RR 0.27 (95% CI 0.17-0.42)], as did lanthanum [RR 0.12 (95% CI 0.05-0.32)]. Sevelamer reduced hospitalizations [RR 0.50 (95% CI 0.31-0.81)], but not lanthanum [RR 0.80 (95% CI 0.34-1.93)]. The presence/absence of other clinically relevant outcomes was infrequently reported. Compared with calcium-based binders, sevelamer reduced serum calcium, low-density lipoprotein and coronary artery calcification, but increased intact parathyroid hormone. The clinical relevance of these changes is unknown since corresponding clinical outcomes were not reported. Lanthanum had less favorable impact on biochemical parameters. Sevelamer hydrochloride and sevelamer carbonate were similar in three studies. Sevelamer was similar to lanthanum (three studies) and iron-based binders (three studies).
Sevelamer was associated with a nonsignificant reduction in mortality and significantly lower hospitalization rates and hypercalcemia compared with calcium-based binders. However, differences in important outcomes, such as cardiac events, fractures, calciphylaxis, hyperchloremic acidosis and health-related quality of life remain understudied. Lanthanum and iron-based binders did not show superiority for any clinically relevant outcomes. Future studies that fail to measure clinically important outcomes (the reason why phosphate binders are prescribed in the first place) will be wasteful.
目前尚不清楚在慢性肾脏病(CKD)高磷血症管理中应首选哪种磷结合剂。
我们对比较司维拉姆或镧与其他磷结合剂用于CKD的随机试验进行了系统评价和荟萃分析。
共纳入51项试验(8829例患者)。与钙基结合剂相比,司维拉姆全因死亡率略低但无统计学意义[风险比(RR)0.62,95%置信区间(CI)0.35 - 1.08],镧全因死亡率亦略低但无统计学意义[RR 0.73,95% CI 0.18 - 3.00],但偏倚风险令人担忧。与钙基结合剂相比,司维拉姆降低了高钙血症风险[RR 0.27,95% CI 0.17 - 0.42],镧也降低了高钙血症风险[RR 0.12,95% CI 0.05 - 0.32]。司维拉姆降低了住院率[RR 0.50,95% CI 0.31 - 0.81],但镧未降低住院率[RR 0.80,95% CI 0.34 - 1.93]。其他临床相关结局的有无很少被报告。与钙基结合剂相比,司维拉姆降低了血清钙、低密度脂蛋白和冠状动脉钙化,但增加了甲状旁腺素原。由于未报告相应的临床结局,这些变化的临床相关性尚不清楚。镧对生化指标的影响较差。在三项研究中,盐酸司维拉姆和碳酸司维拉姆相似。司维拉姆与镧(三项研究)和铁基结合剂(三项研究)相似。
与钙基结合剂相比,司维拉姆与死亡率的非显著性降低相关,住院率和高钙血症显著降低。然而,在重要结局方面,如心脏事件、骨折、钙化防御、高氯性酸中毒和健康相关生活质量的差异仍研究不足。镧和铁基结合剂在任何临床相关结局方面均未显示出优势。未来未能测量临床重要结局(最初开具磷结合剂的原因)的研究将是徒劳的。