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Detection of early renal injury in children with solid tumors undergoing chemotherapy by urinary neutrophil gelatinase-associated lipocalin

机译:尿中性粒细胞明胶酶相关脂质运载蛋白检测儿童接受化疗的实体瘤早期肾脏损伤

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摘要

Acute kidney injury (AKI) is a complication in children with solid tumors undergoing chemotherapy, as it may prevent the use of therapy protocols and also hinder the supportive and diagnostic procedures. Thus, there is an urgent requirement for early predictive biomarkers of AKI. The most promising novel AKI biomarker is neutrophil gelatinase-associated lipocalin (NGAL). The aim of the present study was to compare the predictability of NGAL as a biomarker of AKI with creatinine as a traditional biomarker in children with solid tumors under chemotherapy. The study was performed on 30 patients with different types of solid tumors (reuroblastoma, Wilms tumor, medulloblastoma, rhabdomyosarcoma and Ewing sarcoma) and 20 control subjects. Urinary NGAL (uNGAL) and serum creatinine samples were taken three times: Baseline before the beginning of the treatment, one week after chemotherapy and at the end of the chemotherapy protocol. AKI is defined as a change in creatinine level by >50% of the baseline. The creatinine level only rises to this level in the third sample, while uNGAL increases significantly in the second and third samples with percentage of change 376.8 and 698.2%, respectively, which is highly significant (P<0.001). When comparing the predictive value of serum creatinine for AKI depending on the receiver operating characteristic curve with that of uNGAL, the area under the curve (AUC) for creatinine was 0.60 with a standard error (SE) of 0.086 and 95% confidence interval (CI) between 0.432 and 0.768, while that of uNGAL was highly predictive with an AUC of 0.847, SE 0.55 and 95% CI between 0.739 and 0.955. Depending only on the creatinine level for detecting the AKI will markedly delay the diagnosis; however, uNGAL is detected earlier, and is easier and more reliable as a marker for AKI in children with solid tumors undergoing chemotherapy.
机译:患有实体瘤的儿童在接受化疗的过程中会发生急性肾损伤(AKI),因为它可能会阻止使用治疗方案,还会阻碍支持和诊断程序。因此,迫切需要AKI的早期预测生物标志物。最有前途的新型AKI生物标志物是中性粒细胞明胶酶相关的脂蛋白(NGAL)。本研究的目的是比较化疗后实体瘤患儿中NGAL作为AKI生物标志物与肌酐作为传统生物标志物的可预测性。这项研究是针对30名患有不同类型实体瘤(成神经母细胞瘤,Wilms肿瘤,髓母细胞瘤,横纹肌肉瘤和尤因肉瘤)的患者和20名对照受试者进行的。尿液NGAL(uNGAL)和血清肌酐样本采集了3次:治疗开始前,化疗后1周和化疗方案结束时的基线。 AKI被定义为肌酐水平变化超过基线的50%。肌酐水平仅在第三个样品中上升到该水平,而uNGAL在第二个和第三个样品中显着增加,变化百分比分别为376.8和698.2%,这是非常显着的(P <0.001)。当比较血清肌酐对AKI的预测值(取决于接受者的操作特征曲线)和uNGAL的预测值时,肌酐的曲线下面积(AUC)为0.60,标准误(SE)为0.086,置信区间为95%(CI) )介于0.432和0.768之间,而uNGAL的预测值则具有较高的预测性,AUC为0.847,SE为0.55,95%CI在0.739和0.955之间。仅依靠肌酐水平检测AKI会明显延迟诊断;然而,uNGAL较早发现,并且在接受化疗的实体瘤患儿中作为AKI的标记物更容易,更可靠。

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