Anis Karim H, Pober David, Rosas Sylvia E
Joslin Diabetes Center, Harvard Medical School, Boston, MA.
Kidney Med. 2020 Jun 17;2(4):450-458. doi: 10.1016/j.xkme.2020.05.009. eCollection 2020 Jul-Aug.
RATIONALE & OBJECTIVE: Mineral and bone disorder in chronic kidney disease (CKD) is associated with progression of coronary artery calcification (CAC). Mineral and bone disorder often is treated with calcitriol and other vitamin D receptor activators, including paricalcitol, agents that may have differential effects on calcium, phosphate, and parathyroid hormone levels. Accordingly, we investigated whether these agents have differential effects on CAC progression in patients with CKD.
Randomized, double-concealed, 48-week clinical trial.
SETTING & PARTICIPANTS: CKD stage 3 or 4 with secondary hyperparathyroidism with CAC score > 0 and no prior treatment with activated vitamin D.
Calcitriol versus paricalcitol.
The primary outcome was log-transformed CAC change. Secondary outcomes included percent change in CAC volume, valvular calcifications, and bone mineral metabolism markers.
Among 44 individuals randomly assigned, mean age was 65 years and mean estimated glomerular filtration rate was 27 mL/min/1.73 m. Median CAC score was 140 (IQR, 55-277) Agatston units at baseline. There was no significant difference in CAC progression between treatment arms ( = 0.06). After adjustment for baseline CAC score (log), treatment group remains nonsignificant ( = 0.08). Further adjustment for creatinine level and/or CKD stage did not change the association. In secondary analyses adjusting for dose level of activated vitamin D, treatment group was significant ( = 0.01), and when dose level was also included in the model, the coefficient for individuals in the paricalcitol group was significantly associated with CAC progression ( = 0.02). An interaction term between dosing level and CKD stage was significant at the highest dosing level ( = 0.04).
Pilot single-center study.
In patients with CKD with secondary hyperparathyroidism naive to activated vitamin D therapy, there was no difference in CAC or valvular progression in participants receiving calcitriol compared with paricalcitol during a 48-week period.
Abbvie, Inc.
NCT00752102.
慢性肾脏病(CKD)中的矿物质和骨代谢紊乱与冠状动脉钙化(CAC)进展相关。矿物质和骨代谢紊乱通常用骨化三醇和其他维生素D受体激活剂治疗,包括帕立骨化醇,这些药物可能对钙、磷和甲状旁腺激素水平有不同影响。因此,我们研究了这些药物对CKD患者CAC进展是否有不同影响。
随机、双盲、48周临床试验。
CKD 3或4期伴继发性甲状旁腺功能亢进,CAC评分>0且既往未接受活性维生素D治疗。
骨化三醇与帕立骨化醇对比。
主要观察指标是经对数转换的CAC变化。次要观察指标包括CAC体积百分比变化、瓣膜钙化和骨矿物质代谢标志物。
在随机分配的44名个体中,平均年龄为65岁,平均估计肾小球滤过率为27 mL/min/1.73 m²。基线时CAC评分中位数为140(四分位间距,55 - 277)阿加斯顿单位。各治疗组之间CAC进展无显著差异(P = 0.06)。在对基线CAC评分(对数)进行调整后,治疗组仍无显著差异(P = 0.08)。对肌酐水平和/或CKD分期进行进一步调整并未改变这种关联。在对活性维生素D剂量水平进行调整的次要分析中,治疗组有显著差异(P = 0.01),并且当剂量水平也纳入模型时,帕立骨化醇组个体的系数与CAC进展显著相关(P = 0.02)。给药水平与CKD分期之间的交互项在最高给药水平时有显著差异(P = 0.04)。
单中心试点研究。
在未接受过活性维生素D治疗的继发性甲状旁腺功能亢进的CKD患者中,在48周期间,接受骨化三醇治疗的参与者与接受帕立骨化醇治疗的参与者相比,CAC或瓣膜进展无差异。
艾伯维公司。
NCT00752102。