Salević Petar, Radović Pavle, Milić Nataša, Bogdanović Radovan, Paripović Dušan, Paripović Aleksandra, Golubović Emilija, Milosević Biljana, Mulić Bilsana, Peco-Antić Amira
Medical Faculty, University of Belgrade, Belgrade, Serbia,
J Nephrol. 2014 Oct;27(5):537-44. doi: 10.1007/s40620-014-0094-8. Epub 2014 Apr 23.
Growth retardation is one of the most visible comorbid conditions of chronic kidney disease (CKD) in children. To our knowledge, published data on longitudinal follow-up of growth in pediatric patients with CKD is lacking from the region of South-East Europe. Herein we report the results from the Serbian Pediatric Registry of Chronic Kidney Disease.
The data reported in the present prospective analysis were collected between 2000 and 2012. A total of 324 children with CKD were enrolled in the registry.
Prevalence of growth failure at registry entry was 29.3 %. Mean height standard deviation scores (HtSDS) in children with stunting and those with normal stature were -3.00 [95 % confidence interval (CI) -3.21 to -2.79] and -0.08 (95 % CI -0.22 to 0.05) (p < 0.001), respectively. Children with hereditary nephropathy had worse growth at registration (-1.51; 95 % CI -1.97 to -1.04, p = 0.008). Those with CKD stages 4 and 5 before registration had more chance to have short stature at registration than those with CKD stages 2 and 3 [odds ratio (OR) = 0.458, CI 0.268-0.782, p = 0.004]. Dialysis was an independent negative predictor for maintaining optimal stature during the follow-up period (OR = 0.324, CI = 0.199-0.529, p < 0.001), while transplantation was an independent positive predictor for improvement of small stature during follow-up (OR = 3.706, CI = 1.785-7.696, p < 0.001).
Growth failure remains a significant problem in children with CKD, being worst in patients with hereditary renal disease. Growth is not improved by standard dialysis, but transplantation has a positive impact on growth in children.
生长发育迟缓是儿童慢性肾脏病(CKD)最常见的合并症之一。据我们所知,东南欧地区缺乏关于CKD儿科患者生长发育纵向随访的已发表数据。在此,我们报告塞尔维亚儿童慢性肾脏病登记处的结果。
本前瞻性分析报告的数据收集于2000年至2012年之间。共有324例CKD儿童登记入册。
登记时生长发育不良的患病率为29.3%。发育迟缓儿童和身材正常儿童的平均身高标准差评分(HtSDS)分别为-3.00[95%置信区间(CI)-3.21至-2.79]和-0.08(95%CI-0.22至0.05)(p<0.001)。遗传性肾病儿童登记时生长情况较差(-1.51;95%CI-1.97至-1.04,p=0.008)。登记前处于CKD 4期和5期的儿童比处于CKD 2期和3期的儿童在登记时身材矮小的可能性更大[比值比(OR)=0.458,CI 0.268-0.782,p=0.004]。透析是随访期间维持最佳身高的独立负性预测因素(OR=0.324,CI=0.199-0.529,p<0.001),而移植是随访期间改善身材矮小的独立正性预测因素(OR=3.706,CI=1.785-7.696,p<0.001)。
生长发育迟缓仍是CKD儿童的一个重要问题,在遗传性肾病患者中最为严重。标准透析不能改善生长发育,但移植对儿童生长有积极影响。