Gerber Claire, Harel Miriam, Lynch Miranda L, Herbst Katherine W, Ferrer Fernando A, Shapiro Linda H
Center for Vascular Biology, University of Connecticut Health Center, Farmington, CT, USA.
Center for Vascular Biology, University of Connecticut Health Center, Farmington, CT, USA; Division of Urology, Department of Surgery, Connecticut Children's Medical Center, Hartford, CT, USA.
J Pediatr Urol. 2016 Apr;12(2):120.e1-7. doi: 10.1016/j.jpurol.2015.10.008. Epub 2015 Nov 28.
Ureteropelvic junction obstruction (UPJO) is the major cause of hydronephrosis in children and may lead to renal injury and early renal dysfunction. However, diagnosis of the degree of obstruction and severity of renal injury relies on invasive and often inconclusive renal scans. Biomarkers from voided urine that detect early renal injury are highly desirable because of their noninvasive collection and their potential to assist in earlier and more reliable diagnosis of the severity of obstruction. Early in response to UPJO, increased intrarenal pressure directly impacts the proximal tubule brush border. We hypothesize that single-pass, apically expressed proximal tubule brush border proteins will be shed into the urine early and rapidly and will be reliable noninvasive urinary biomarkers, providing the tools for a more reliable stratification of UPJO patients.
We performed a prospective cohort study at Connecticut Children's Medical Center. Bladder urine samples from 12 UPJO patients were obtained prior to surgical intervention. Control urine samples were collected from healthy pediatric patients presenting with primary nocturnal enuresis. We determined levels of NGAL, KIM-1 (previously identified biomarkers), CD10, CD13, and CD26 (potentially novel biomarkers) by ELISA in control and experimental urine samples. Urinary creatinine levels were used to normalize the urinary protein levels measured by ELISA.
Each of the proximal tubule proteins outperformed the previously published biomarkers. No differences in urinary NGAL and KIM-1 levels were observed between control and obstructed patients (p = 0.932 and p = 0.799, respectively). However, levels of CD10, CD13, and CD26 were significantly higher in the voided urine of obstructed individuals when compared with controls (p = 0.002, p = 0.024, and p = 0.007, respectively) (Figure).
Targeted identification of reliable, noninvasive biomarkers of renal injury is critical to aid in diagnosing patients at risk, guiding therapeutic decisions and monitoring treatment efficacy. Proximal tubule brush border proteins are reliably detected in the urine of obstructed patients and may be more effective at predicting UPJO.
肾盂输尿管连接部梗阻(UPJO)是儿童肾积水的主要原因,可能导致肾损伤和早期肾功能障碍。然而,梗阻程度和肾损伤严重程度的诊断依赖于侵入性且往往不确定的肾脏扫描。由于其非侵入性采集以及有助于更早、更可靠地诊断梗阻严重程度的潜力,检测早期肾损伤的晨尿生物标志物非常可取。在对UPJO的早期反应中,肾内压力升高直接影响近端小管刷状缘。我们假设,单次通过、顶端表达的近端小管刷状缘蛋白会早期快速地排入尿液,并且将成为可靠的非侵入性尿液生物标志物,为更可靠地对UPJO患者进行分层提供工具。
我们在康涅狄格州儿童医疗中心进行了一项前瞻性队列研究。在手术干预前,从12例UPJO患者中获取膀胱尿液样本。对照尿液样本取自患有原发性夜间遗尿症的健康儿科患者。我们通过酶联免疫吸附测定法(ELISA)测定对照和实验尿液样本中中性粒细胞明胶酶相关脂质运载蛋白(NGAL)、肾损伤分子-1(KIM-1,先前已鉴定的生物标志物)、CD10、CD13和CD26(潜在的新型生物标志物)的水平。尿肌酐水平用于标准化ELISA测定的尿蛋白水平。
每种近端小管蛋白的表现均优于先前发表的生物标志物。对照患者和梗阻患者之间未观察到尿NGAL和KIM-1水平的差异(分别为p = 0.932和p = 0.799)。然而,与对照组相比,梗阻个体晨尿中CD10、CD13和CD26的水平显著更高(分别为p = 0.002、p = 0.024和p = 0.007)(图)。
靶向识别可靠的肾损伤非侵入性生物标志物对于帮助诊断有风险的患者、指导治疗决策和监测治疗效果至关重要。在梗阻患者的尿液中可可靠检测到近端小管刷状缘蛋白,并且在预测UPJO方面可能更有效。