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Clin J Am Soc Nephrol. 2017 Dec 7;12(12):1930-1940. doi: 10.2215/CJN.03030317. Epub 2017 Oct 26.
Epidemiologic studies suggest that higher serum phosphaturic hormone fibroblast growth factor 23 levels are associated with increase morbidity and mortality. The aim of the FGF23 Reduction Efficacy of a New Phosphate Binder in CKD Trial was to evaluate the effect of sevelamer carbonate on serum C-terminal fibroblast growth factor 23 levels in normophosphatemic patients with CKD stage 3b/4.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Patients with CKD, eGFR between 45 and 15 ml/min per 1.73 m, fasting serum phosphate concentration >3.1 mg/dl, and serum C-terminal fibroblast growth factor 23 >80 relative units/ml were included in our double-blind, placebo-controlled, randomized multicenter study. All patients received 100,000 IU cholecalciferol at time of randomization. Participants received either placebo or sevelamer carbonate 4.8 g daily during a 12-week period. Biologic parameters, including serum C-terminal fibroblast growth factor 23, intact fibroblast growth factor 23, and -klotho, were evaluated at baseline and 12 weeks after inclusion.
Of 96 screened patients, 78 (mean±SD age: 63±13 years old; 70% men; mean eGFR: 27±9 ml/min per 1.73 m) met the inclusion criteria. At baseline, mean eGFR was 27±9 ml/min per 1.73 m, mean serum phosphate level was 3.8±0.5 mg/dl, and median (interquartile range) serum C-terminal fibroblast growth factor 23 level was 157 (120-241) relative units/ml. After 12 weeks of treatment, urinary phosphate-to-creatinine ratio fell significantly in the sevelamer group. The sevelamer and placebo groups did not differ significantly in terms of median change in serum C-terminal fibroblast growth factor 23 levels: the median (interquartile range) change was 38 (-13-114) relative units/ml in the placebo group and 37 (-1-101) relative units/ml in the sevelamer group (=0.77). There was no significant difference in serum intact fibroblast growth factor 23, -klotho, or phosphate levels changes between the two groups. Serum total and LDL cholesterol levels fell significantly in the sevelamer group.
In our double-blind, placebo-controlled, randomized study performed in normophosphatemic patients with CKD, a 12-week course of sevelamer carbonate significantly reduced phosphaturia without changing serum phosphorus but did not significantly modify serum C-terminal fibroblast growth factor 23 and intact fibroblast growth factor 23 or -klotho levels.
流行病学研究表明,较高的血清磷酸激素成纤维细胞生长因子 23 水平与发病率和死亡率的增加有关。在 FGF23 减少慢性肾脏病中新型磷酸盐结合剂疗效的研究中,目的是评估碳酸司维拉姆对血清 C 末端成纤维细胞生长因子 23 水平的影响在患有 CKD 3b/4 期的正常血磷患者中。
设计、地点、参与者和测量:包括患有 CKD、eGFR 在 45 至 15 ml/min/1.73 m 之间、空腹血清磷酸盐浓度>3.1 mg/dl 和血清 C 末端成纤维细胞生长因子 23>80 相对单位/ml 的患者在内的我们的这项双盲、安慰剂对照、随机多中心研究。所有患者在随机分组时均接受 100000 IU 胆钙化醇。参与者在 12 周期间每天接受安慰剂或碳酸司维拉姆 4.8 g。在基线和纳入后 12 周评估生物学参数,包括血清 C 末端成纤维细胞生长因子 23、完整成纤维细胞生长因子 23 和 -klotho。
在 96 名筛选患者中,有 78 名(平均年龄±标准差:63±13 岁;70%为男性;平均 eGFR:27±9 ml/min/1.73 m)符合纳入标准。在基线时,平均 eGFR 为 27±9 ml/min/1.73 m,平均血清磷酸盐水平为 3.8±0.5 mg/dl,中位数(四分位距)血清 C 末端成纤维细胞生长因子 23 水平为 157(120-241)相对单位/ml。经过 12 周的治疗,司维拉姆组的尿磷肌酐比显著下降。司维拉姆组和安慰剂组在血清 C 末端成纤维细胞生长因子 23 水平的中位数变化方面无显著差异:安慰剂组的中位数(四分位距)变化为 38(-13-114)相对单位/ml,司维拉姆组为 37(-1-101)相对单位/ml(=0.77)。两组之间血清完整成纤维细胞生长因子 23、-klotho 和磷酸盐水平的变化无显著差异。司维拉姆组的血清总胆固醇和 LDL 胆固醇水平显著下降。
在我们对患有 CKD 的正常血磷患者进行的这项双盲、安慰剂对照、随机研究中,碳酸司维拉姆治疗 12 周可显著减少磷的排泄,而不改变血清磷,但对血清 C 末端成纤维细胞生长因子 23 和完整成纤维细胞生长因子 23 或 -klotho 水平没有显著影响。