A Randomized Multicenter Trial of Paricalcitol versus Calcitriol for Secondary Hyperparathyroidism in Stages 3-4 CKD

被引:51
作者
Coyne, Daniel W. [1 ]
Goldberg, Seth [1 ]
Faber, Mark [2 ]
Ghossein, Cybele [3 ]
Sprague, Stuart M. [4 ]
机构
[1] Washington Univ, Sch Med, Div Renal, St Louis, MO 63110 USA
[2] Henry Ford Hosp, Div Nephrol & Hypertens, Detroit, MI 48202 USA
[3] Northwestern Univ, Div Nephrol, Feinberg Sch Med, Chicago, IL 60611 USA
[4] Univ Chicago, Div Nephrol & Hypertens, Northshore Univ Hlth Syst, Pritzker Sch Med, Evanston, IL USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2014年 / 9卷 / 09期
关键词
CHRONIC KIDNEY-DISEASE; D-RECEPTOR ACTIVATION; VITAMIN-D; INTESTINAL CALCIUM; PTH LEVELS; HEMODIALYSIS; PHOSPHORUS; ERGOCALCIFEROL; ASSOCIATION; MORTALITY;
D O I
10.2215/CJN.10661013
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives Calcitriol is used to treat secondary hyperparathyroidism in patients with CKD. Paricalcitol is less calcemic and phosphatemic in preclinical studies and in some trials in dialysis patients, but head-to-head comparisons in nondialysis patients are lacking. A large meta-analysis of trials concluded that these agents did not consistently reduce parathyroid hormone (PTH) and increased the risk of hypercalcemia and hyperphosphatemia. Therefore, the objective of this multicenter trial was to compare the rate of hypercalcemia between calcitriol and paricalcitol, while suppressing PTH 40%-60%. Design, setting, participants, & measurements Patients with stages 3 4 CKD (n=110) with a PTH level >120 pg/ml were recruited and randomized to 0.25 mu g/d of calcitriol or 1 mu g/d of paricalcitol between April 2009 and July 2011. Subsequent dose adjustments were by protocol to achieve 40%-60% PTH suppression below baseline. The primary endpoint was the rate of confirmed hypercalcemia of >10.5 mg/dl between groups. Results Forty-five patients in each group completed the 24 weeks of treatment. Both agents suppressed PTH effectively (-52% with paricalcitol and -46% with calcitriol; P=0.17), although the paricalcitol group reached a 40% reduction in PTH sooner at a median 8 weeks (interquartile range [IQR], 4, 12) versus 12 weeks (IQR, 8, 18; P=0.02) and had a lower pill burden of 240 (IQR, 180, 298) versus 292 (IQR, 231, 405; P=0.01). Confirmed hypercalcemia was very low in both groups (three with paricalcitol and one with cacitriol) and was not significantly different (P=0.36). Both groups had small increases in calcium and phosphorus levels (0.3-0.4 mg/dl in each electrolyte) and significant decreases in alkaline phosphatase, a marker of high bone turnover, with no significant differences between groups. Conclusions These results show that both calcitriol and paricalcitol achieved sustained PTH and alkaline phosphatase suppression in stages 3-4 CKD, with small effects on serum calcium and phosphorus and a low incidence of hypercalcemia.
引用
收藏
页码:1620 / 1626
页数:7
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