Division of Nephrology, Endocrinology and Metabolism, Tokai University School of Medicine, Isehara, Japan.
Nephrol Dial Transplant. 2012 Feb;27(2):784-90. doi: 10.1093/ndt/gfr384. Epub 2011 Jul 5.
Elevated fibroblast growth factor 23 (FGF23) is associated with adverse clinical outcomes and development of secondary hyperparathyroidism (SHPT) refractory to active vitamin D. Cinacalcet hydrochloride is effective in treating SHPT, but little is known as to whether treatment with cinacalcet alters these levels and whether pretreatment FGF23 levels predict response to this therapy.
We measured serum full-length FGF23 levels in 55 haemodialysis patients, who participated and completed the 52-week, multicentre, open-label single-arm trial that examined the effectiveness of cinacalcet for treating SHPT. In the study, alteration of vitamin D dosage was not permitted except for the case in which serum calcium could not be managed by calcium carbonate adjustment alone.
After 12 weeks of cinacalcet treatment, FGF23 levels decreased significantly concomitantly with a significant reduction in intact parathyroid hormone (PTH) levels. These responses were sustained >52 weeks. In multivariate regression analyses, changes from baseline in serum FGF23 were associated with changes in serum calcium and phosphorus but not with intact PTH at each time point of measurements (Week-12, Week-24 and Week-52). Baseline FGF23 was not associated with the likelihood of achieving an intact PTH <180 pg/mL at the study end.
Cinacalcet lowers serum FGF23 in haemodialysis patients with SHPT independently of the effects of active vitamin D. Pretreatment FGF23 cannot predict treatment response to cinacalcet in this setting. The precise mechanism of FGF23 reduction by cinacalcet and its clinical impact on outcomes in patients remain to be investigated.
成纤维细胞生长因子 23(FGF23)升高与不良临床结局和继发甲状旁腺功能亢进症(SHPT)的发生有关,而后者对活性维生素 D 治疗抵抗。盐酸西那卡塞在治疗 SHPT 方面是有效的,但对于治疗是否会改变这些水平以及治疗前 FGF23 水平是否能预测对该治疗的反应,我们知之甚少。
我们测量了 55 例血液透析患者的血清全长 FGF23 水平,这些患者参加并完成了一项为期 52 周、多中心、开放标签的单臂试验,该试验研究了盐酸西那卡塞治疗 SHPT 的有效性。在该研究中,除了仅通过碳酸钙调整不能控制血清钙的情况外,不允许改变维生素 D 剂量。
在盐酸西那卡塞治疗 12 周后,FGF23 水平显著降低,同时完整甲状旁腺激素(PTH)水平显著降低。这些反应持续>52 周。在多变量回归分析中,血清 FGF23 从基线的变化与血清钙和磷的变化相关,但与每个测量时间点的完整 PTH 无关(第 12 周、第 24 周和第 52 周)。基线 FGF23 与研究结束时达到完整 PTH<180pg/ml 的可能性无关。
盐酸西那卡塞可降低血液透析伴 SHPT 患者的血清 FGF23,独立于活性维生素 D 的作用。治疗前 FGF23 不能预测该患者使用盐酸西那卡塞的治疗反应。西那卡塞降低 FGF23 的精确机制及其对患者结局的临床影响仍有待研究。