Department of Urology Surgery, Qilu Children's Hospital of Shandong University, Jinan, Shandong, China.
Eur Rev Med Pharmacol Sci. 2017 Sep;21(18):4141-4146.
Congenital hydronephrosis is induced by congenital obstruction of uretero pelvic junction, bladder vesicoureteral reflux, posterior urethral valve, stricture of ureter end and ureterocyst, which is extremely apt to cause end-stage renal failure in children. It becomes significant to explore the expression profile and clinical significance of aquaporin-1 (AQP-1) and ET-1 (endothelin-1) in the urine of children with congenital hydronephrosis.
80 cases of children with congenital hydronephrosis were selected to be the observation group and another 40 cases of children with other diseases were served as control group. Pre-operative morning urine, intra-operative renal pelvis urine and morning urine at the 7th day after the operation of all the children were collected for the detection of the level of ET-1, Cr level and AQP1 in the urine. Urine various indexes of different diseases stages in children of both groups were compared.
There was no significant difference between children with mild and children in control group (p > 0.05). In the observation group, the AQP-1 level during the operation was significantly lower than that before operation, but it was significantly higher in post-operation than that during the operation, which was still lower than that in control group (p < 0.05). Urine ET-1 level in observation group and its positive rate were significantly higher than that in control group (p < 0.05). Serum stress indexes in each stage of the observation group were significantly higher than that in control group (p < 0.05).
The expression levels of urine AQP-1 and ET-1 of children with congenital hydronephrosis were obviously increased. The AQP-1 level during the operation was lower than that before operation. This post-operation level was significantly higher than before the operation. The expression of AQP-1 and ET-1 could be used as important indexes for clinical diagnosis.
先天性肾积水是由输尿管肾盂交界处先天性梗阻、膀胱输尿管反流、后尿道瓣膜、输尿管末端和输尿管狭窄引起的,极易导致儿童终末期肾衰竭。探讨先天性肾积水患儿尿液中水通道蛋白-1(AQP-1)和内皮素-1(ET-1)的表达谱及其临床意义具有重要意义。
选择 80 例先天性肾积水患儿为观察组,另选同期 40 例其他疾病患儿为对照组。采集所有患儿术前晨尿、术中肾盂尿和术后第 7 天晨尿,检测尿液 ET-1 水平、Cr 水平和 AQP1。比较两组患儿不同疾病阶段的尿液各项指标。
观察组轻度肾积水患儿与对照组比较差异无统计学意义(p>0.05)。观察组术中 AQP-1 水平明显低于术前,但术后明显高于术中,仍低于对照组(p<0.05)。观察组尿液 ET-1 水平及其阳性率明显高于对照组(p<0.05)。观察组各期血清应激指标均明显高于对照组(p<0.05)。
先天性肾积水患儿尿液 AQP-1 和 ET-1 表达水平明显升高,术中 AQP-1 水平低于术前,术后明显高于术前。AQP-1 和 ET-1 的表达可作为临床诊断的重要指标。