Division of Nephrology, Endocrinology and Metabolism, Tokai University School of Medicine, Isehara, Japan.
Nephrol Dial Transplant. 2012 May;27(5):1967-9. doi: 10.1093/ndt/gfr645. Epub 2011 Dec 1.
Klotho is a transmembrane protein that acts as a cofactor for fibroblast growth factor 23 (FGF23). Klotho also exists as a soluble circulating protein, but its role in secondary hyperparathyroidism (SHPT) is largely unknown.
We measured serum soluble Klotho levels in 51 haemodialysis patients, who participated and completed a 52-week, multicentre, open-label single-arm trial that examined the effectiveness of cinacalcet for treating SHPT.
After 12 weeks of cinacalcet treatment, serum soluble Klotho decreased significantly (P = 0.03) but only marginally from 398 pg/mL [interquartile range (IQR), 268-588 pg/mL] to 378 pg/mL (IQR, 266-568 pg/mL) and returned to baseline levels. There were no significant associations between the changes in soluble Klotho levels and changes in any other parameters of mineral metabolism, including serum calcium, phosphorus, intact parathyroid hormone and FGF23.
Despite significant alterations in mineral and bone metabolism during treatment with cinacalcet, this resulted in only small and transient reductions in serum levels of soluble Klotho.
Klotho 是一种跨膜蛋白,作为成纤维细胞生长因子 23(FGF23)的辅助因子发挥作用。Klotho 也存在可溶性循环蛋白,但它在继发性甲状旁腺功能亢进症(SHPT)中的作用在很大程度上尚不清楚。
我们测量了 51 名血液透析患者的血清可溶性 Klotho 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,该试验研究了西那卡塞治疗 SHPT 的疗效。
西那卡塞治疗 12 周后,血清可溶性 Klotho 显著下降(P=0.03),但仅从 398pg/mL[四分位间距(IQR),268-588pg/mL]降至 378pg/mL(IQR,266-568pg/mL),并恢复到基线水平。可溶性 Klotho 水平的变化与矿物质代谢的任何其他参数的变化之间均无显著关联,包括血清钙、磷、全段甲状旁腺激素和 FGF23。
尽管在西那卡塞治疗期间矿物质和骨代谢发生了显著改变,但这仅导致血清可溶性 Klotho 水平出现微小而短暂的降低。