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使用磷酸盐结合疗法降低慢性肾脏病患者血清成纤维细胞生长因子23水平:司维拉姆降低FGF23试验(SoFT)的原理与研究设计

Phosphate Binding Therapy to Lower Serum Fibroblast-Growth-Factor-23 Concentrations in Chronic Kidney Disease: Rationale and Study Design of the Sevelamer on FGF23 Trial (SoFT).

作者信息

Adema Aaltje Y, de Jong Maarten A, de Borst Martin H, Ter Wee Pieter M, Vervloet Marc G

出版信息

Nephron. 2016;134(4):215-220. doi: 10.1159/000448184. Epub 2016 Jul 22.

Abstract

BACKGROUND

Increased levels of phosphate and fibroblast growth factor-23 (FGF23) are strong predictors of cardiovascular morbidity and mortality in patients with chronic kidney disease (CKD). Preliminary data suggest that interventions lowering gastro-intestinal phosphate uptake lowers serum FGF23 concentrations and improves cardiovascular risk and subsequently survival. However, data are lacking about the magnitude of effects, the effect in different stages of CKD and whether there is a dose-effect relationship.

METHODS

Therefore, the Sevelamer on FGF23 Trial (SoFT) is designed as an open-label, single-arm, clinical pilot study aiming to demonstrate the feasibility of a phosphate-restricted diet in combination with the phosphate binder sevelamer to induce an effective, predictable and sustained decrease in FGF23 level in patients with an estimated glomerular filtration rate (eGFR) of 15-90 or >90 ml/min/1.73 m2 with proteinuria >1.0 g in 24 h urine collection, despite optimally dosed RAAS blockade, without inducing hypophosphatemia using a forced uptitration treatment regimen aimed at restricting phosphate uptake.

摘要

背景

在慢性肾脏病(CKD)患者中,磷酸盐和成纤维细胞生长因子23(FGF23)水平升高是心血管疾病发病率和死亡率的有力预测指标。初步数据表明,降低胃肠道磷酸盐摄取的干预措施可降低血清FGF23浓度,改善心血管风险并进而提高生存率。然而,关于效应大小、在CKD不同阶段的效应以及是否存在剂量效应关系的数据尚缺。

方法

因此,司维拉姆对FGF23的试验(SoFT)设计为一项开放标签、单臂临床试验,旨在证明在估计肾小球滤过率(eGFR)为15 - 90或>90 ml/min/1.73 m²、24小时尿蛋白>1.0 g的患者中,限制磷酸盐饮食联合磷酸盐结合剂司维拉姆可有效、可预测且持续降低FGF23水平的可行性,尽管已使用最佳剂量的肾素 - 血管紧张素 - 醛固酮系统(RAAS)阻滞剂,且采用旨在限制磷酸盐摄取的强制滴定治疗方案,不诱导低磷血症。

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