Battistella M, Richardson R M A, Bargman J M, Chan C T
Division of Nephrology, Department of Medicine, University Health Network, Toronto, ON, Canada.
Clin Nephrol. 2011 Aug;76(2):99-103. doi: 10.5414/cn106640.
Uncontrolled hy-per-parathyroidism causes bone marrow fibrosis, leading to erythropoietin (EPO) resistance. Medical treatment with cinacalcet is effective in reducing plasma parathyroid hormone (PTH) levels, but its effect on darbepoetin dosing is unknown.
We conducted a retrospective cohort study of 40 end-stage renal disease (ESRD) patients (age: 55 ± 14; mean ± SD; 21:male) who had at least 12 months of cinacalcet therapy. The distribution of renal replacement therapies were: 14 peritoneal dialysis, 18 conventional hemodialysis and 8 nocturnal hemodialysis. Standard dialysis related biochemical indices and medications used were recorded. The primary objective of the study was to ascertain the difference in darbepoetin responsiveness before and after 12 months of cinacalcet therapy. Our secondary objective was to determine if there was a relationship between the changes in PTH and darbepoetin requirement.
Overall, PTH levels decreased from 197.5 (151.8; 249.2) to 66.1 (41.2; 136.5) (median (25th;75th percentile)) pmol/l; p < 0.001. Cinacalcet dose increased from 30.0 ± 6 to 63 ± 25 mg/day, p < 0.05. Hemoglobin remained unchanged (116 ± 13 to 116 ± 13 g/l), while darbepoetin requirement decreased from 40 (20; 60) to 24 (19; 59) μg/week, p = 0.02. The remainder of the dialysis-related biochemistry (electrolytes, calcium, phosphate, iron status) and vitamin D use remained unchanged. A reduction in PTH level of greater than 30% was experienced by 82.5% (33/40) of our cohort. Among the responders, the fall in PTH and reduction darbepoetin requirement were related (R = -0.48, p = 0.004).
Reduction of PTH by cinacalcet is associated with a decrease in darbepoetin requirement. The interface between bone and bone marrow in uremia represents a critical step in red blood cell production which merits further investigation.
未控制的甲状旁腺功能亢进会导致骨髓纤维化,进而引起促红细胞生成素(EPO)抵抗。西那卡塞药物治疗在降低血浆甲状旁腺激素(PTH)水平方面有效,但它对达贝泊汀剂量的影响尚不清楚。
我们对40例接受至少12个月西那卡塞治疗的终末期肾病(ESRD)患者(年龄:55±14;均值±标准差;男性21例)进行了一项回顾性队列研究。肾脏替代治疗的分布情况为:14例腹膜透析,18例常规血液透析和8例夜间血液透析。记录了标准的透析相关生化指标和使用的药物。该研究的主要目的是确定西那卡塞治疗12个月前后达贝泊汀反应性的差异。我们的次要目的是确定PTH变化与达贝泊汀需求之间是否存在关联。
总体而言,PTH水平从197.5(151.8;249.2)(中位数(第25;75百分位数))pmol/L降至66.1(41.2;136.5)pmol/L;p<0.001。西那卡塞剂量从30.0±6mg/天增加至63±25mg/天,p<0.