Segura Torres Pilar, Borrego Utiel F J, Sánchez Perales M C, García Cortés M J, Biechy Baldán M M, Pérez Bañasco V
Servicio de Nefrología, Complejo Hospitalario de Jaén, Jaén (España).
Nefrologia. 2010;30(4):443-51. doi: 10.3265/Nefrologia.pre2010.May.10451.
Treatment of secondary hyperparathyroidism with cinacalcet improves control of PTH, phosphorus, calcium and Ca x P product, enabling to achieve targets recommended by K/DOQI guidelines for PTHi in only 30-50% of patients, in studies with a very selected population. The aim of this study was to analyze its effectiveness in real clinical practice, comparing results with targets recommended by K/DOQI and KDIGO guidelines and to investigate factors having influence on PTH responsiveness to cinacalcet.
We collected data of evolution of 74 patients on hemodialysis with secondary hyperparathyroidism who were treated with cinacalcet for at least 6 months.
According K/DOQI targets we observed a reduction of proportion of patients with PTHi > 300 pg/ml to 50%, a decrease of hyperphosphoremia from 38.4% to 23.3% and proportion of patients with Ca x P product > 55 mg2/dl2 from 37.8% to 15.1%. By contrast, presence of hypocalcemia increases from 2.7% to 12.3%. Comparing with KDIGO targets, proportion of patients with PTHi > 600 pg/ml decreased from 41.1% to 16.4% and with hyperphosphoremia from 68.5% to 52.1%. However, when considering patients with baseline PTHi > 600 pg/ml prevalence of P > 4.5 mg/dl decreased from 83.3% to 55.2%. We observed significant changes of phosphate binders after cinacalcet treatment with an increase in calcium carbonate doses (pre 0.61 +/- 1.53 g of calcium/day vs post-cinacalcet 0.95 +/- 1.98 g of calcium/day; p = 0.03) that was prescribed to prevent hypocalcemia and not as phosphate binder. Responsiveness were lower in patients who were taking higher doses of sevelamer at baseline, showing at the end of the study higher PTHi (no-sevelamer: 312 +/- 245 pg/ml; sevelamer < 6.4 g/day: 510 +/- 490 pg/ml; sevelamer > 6.4 g/day: 526 +/- 393 pg/ml; p = 0.04) and phosphorus (no-sevelamer: 4.5 +/- 1.2 mg/dl; sevelamer < 6.4 g/day: 4.2 +/- 1.5 mg/dl; sevelamer > 6.4 g/day: 5.7 +/- 0.9 mg/dl; p=0.01) serum levels. Use of paricalcitol did not show any influence on PTH response. Patients achieving targets for PTH at the end of the study showed a good response early, with a significant decrease of PTHi levels at three months (159 +/- 84 vs 630 +/- 377 pg/ml; p < 0.001) with significantly lower doses of cinacalcet (33.8 +/- 22.5 vs 51.1 +/- 25.1 mg/day; p = 0.003). Using multivariate analysis we found that percent of PTHi reduction was related with baseline PTHi levels and taking sevelamer as phosphate binder at baseline.
Use of cinacalcet improves grade of control of secondary hyperparathyroidism in non-selected patients in hemodialysis, showing poor response in population with higher PTHi levels and who takes higher doses of sevelamer at baseline. By contrast, a reduction of PTHi levels at 3 months of treatment with relatively lower doses is a pronostic marker of good response to cinacalcet treatment.
在针对特定人群的研究中,使用西那卡塞治疗继发性甲状旁腺功能亢进可改善甲状旁腺激素(PTH)、磷、钙及钙磷乘积的控制情况,仅30% - 50%的患者能够达到美国肾脏病基金会(K/DOQI)指南针对继发性甲状旁腺功能亢进(PTHi)推荐的目标。本研究旨在分析其在实际临床实践中的有效性,将结果与K/DOQI和改善全球肾脏病预后组织(KDIGO)指南推荐的目标进行比较,并探究影响PTH对西那卡塞反应性的因素。
我们收集了74例接受血液透析的继发性甲状旁腺功能亢进患者的数据,这些患者接受西那卡塞治疗至少6个月。
根据K/DOQI目标,我们观察到PTHi>300 pg/ml的患者比例降至50%,高磷血症从38.4%降至23.3%,钙磷乘积>55 mg²/dl²的患者比例从37.8%降至15.1%。相比之下,低钙血症的发生率从2.7%升至12.3%。与KDIGO目标相比,PTHi>600 pg/ml的患者比例从41.1%降至16.4%,高磷血症从68.5%降至52.1%。然而,对于基线PTHi>600 pg/ml的患者,血磷>4.5 mg/dl的患病率从83.3%降至55.2%。我们观察到西那卡塞治疗后磷结合剂有显著变化,碳酸钙剂量增加(西那卡塞治疗前每日钙0.61±1.53 g,西那卡塞治疗后每日钙0.95±1.98 g;p = 0.03),增加碳酸钙剂量是为预防低钙血症而非作为磷结合剂。基线时服用较高剂量司维拉姆的患者反应性较低,研究结束时其PTHi水平较高(未服用司维拉姆:312±245 pg/ml;司维拉姆<6.4 g/天:510±490 pg/ml;司维拉姆>6.4 g/天:526±393 pg/ml;p = 0.04),血磷水平也较高(未服用司维拉姆:4.5±1.2 mg/dl;司维拉姆<6.4 g/天:4.2±1.5 mg/dl;司维拉姆>6.4 g/天:5.7±0.9 mg/dl;p = 0.01)。使用帕立骨化醇对PTH反应无任何影响。在研究结束时达到PTH目标的患者早期反应良好,3个月时PTHi水平显著下降(159±84 vs 630±377 pg/ml;p<0.001),且西那卡塞剂量显著降低(33.8±22.5 vs 51.1±25.1 mg/天;p = 0.003)。通过多变量分析,我们发现PTHi降低的百分比与基线PTHi水平以及基线时使用司维拉姆作为磷结合剂有关。
在未经过挑选的血液透析患者中,使用西那卡塞可改善继发性甲状旁腺功能亢进的控制程度,对于基线PTHi水平较高且服用较高剂量司维拉姆的人群反应较差。相比之下,治疗3个月时使用相对较低剂量的西那卡塞使PTHi水平降低是对西那卡塞治疗反应良好的一个预后指标。