Meena Jitendra, Thergaonkar Ranjeet W, Sinha Aditi, Lakshmy R, Bagga Arvind, Hari Pankaj
Division of Nephrology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Department of Pediatrics, Command Hospital, Kolkata, India.
Int Urol Nephrol. 2025 Jun 29. doi: 10.1007/s11255-025-04623-x.
Reducing proteinuria in children with chronic kidney disease (CKD) has been shown to slow the progression of kidney damage. Hence, we examined the efficacy of a combination of calcitriol and enalapril as compared to enalapril alone in reducing proteinuria in children with CKD.
Children aged 3 to 18 years with CKD and proteinuria > 250 mg/m/day were randomized to receive enalapril (0.6 mg/kg/daily) with or without calcitriol (0.25 µg twice weekly) for 6 months. Children with estimated GFR (eGFR) < 30 ml/min/1.73 m, serum calcium > 10.5 mg/dl, and phosphate > 5.5 mg/dl were excluded. A primary outcome was a mean difference in the change in proteinuria at 6 months compared to baseline. Secondary outcomes included changes in PTH and eGFR.
Of 212 screened children with CKD and proteinuria, 72 (56 boys, mean age 11.2 ± 3.4 yr) were randomized. Baseline characteristics were similar in both groups. Proteinuria decreased from the baseline to the end of therapy by median 1.05 (IQR: 0.04 to 1.87) g/day with the combination therapy as compared to median 0.49 (IQR: 0.03 to 1.33) g/day in enalapril group (P = 0.54). The percentage reduction in proteinuria was 60.4% with the combination therapy and 50.1% with enalapril therapy (P = 0.48). Three patients developed hyperphosphatemia in enalapril therapy; hypercalcemia and hyperkalemia were not observed.
In children with CKD, the combination of calcitriol and enalapril did not result in significant reduction in proteinuria than enalapril alone. Combination therapy was tolerated well. Further studies with a larger sample size and a longer duration of follow-up studies are needed. Trial registration https://ctri.nic.in CTRI/2011/10/002086. Registered in October 21, 2011.
已证明降低慢性肾脏病(CKD)患儿的蛋白尿可减缓肾脏损害的进展。因此,我们比较了骨化三醇与依那普利联合用药和单独使用依那普利在降低CKD患儿蛋白尿方面的疗效。
将年龄在3至18岁、患有CKD且蛋白尿>250mg/m²/天的儿童随机分为两组,分别接受依那普利(0.6mg/kg/天)联合或不联合骨化三醇(0.25μg,每周两次)治疗6个月。排除估计肾小球滤过率(eGFR)<30ml/min/1.73m²、血清钙>10.5mg/dl以及磷酸盐>5.5mg/dl的儿童。主要结局是与基线相比,6个月时蛋白尿变化的平均差异。次要结局包括甲状旁腺激素(PTH)和eGFR的变化。
在212名筛查出的患有CKD和蛋白尿的儿童中,72名(56名男孩,平均年龄11.2±3.4岁)被随机分组。两组的基线特征相似。联合治疗组蛋白尿从基线降至治疗结束时的中位数为1.05(四分位间距:0.04至1.87)g/天,依那普利组为中位数0.49(四分位间距:0.03至1.33)g/天(P=0.54)。联合治疗组蛋白尿降低百分比为60.4%,依那普利治疗组为50.1%(P=0.48)。依那普利治疗组有3名患者发生高磷血症;未观察到高钙血症和高钾血症。
在CKD患儿中,骨化三醇与依那普利联合用药在降低蛋白尿方面并不比单独使用依那普利有显著效果。联合治疗耐受性良好。需要进行更大样本量和更长随访时间的进一步研究。试验注册:https://ctri.nic.in CTRI/2011/10/002086。于2011年10月21日注册。