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本文引用的文献

1
Urine biomarkers predict acute kidney injury in newborns.尿液生物标志物可预测新生儿急性肾损伤。
J Pediatr. 2012 Aug;161(2):270-5.e1. doi: 10.1016/j.jpeds.2012.02.007. Epub 2012 Mar 16.
2
Acute kidney injury biomarkers: renal angina and the need for a renal troponin I.急性肾损伤生物标志物:肾绞痛和肾肌钙蛋白 I 的需求。
BMC Med. 2011 Dec 21;9:135. doi: 10.1186/1741-7015-9-135.
3
Role of circulating fibroblast growth factor-2 in lipopolysaccharide-induced acute kidney injury in mice.循环成纤维细胞生长因子-2 在脂多糖诱导的小鼠急性肾损伤中的作用。
Pediatr Nephrol. 2012 Mar;27(3):469-83. doi: 10.1007/s00467-011-2001-z. Epub 2011 Sep 30.
4
Acute kidney injury in children: prevention, treatment and rehabilitation.儿童急性肾损伤:预防、治疗与康复
Contrib Nephrol. 2011;174:163-172. doi: 10.1159/000329394. Epub 2011 Sep 9.
5
Urine biomarkers predict acute kidney injury and mortality in very low birth weight infants.尿生物标志物可预测极低出生体重儿的急性肾损伤和死亡率。
J Pediatr. 2011 Dec;159(6):907-12.e1. doi: 10.1016/j.jpeds.2011.05.045. Epub 2011 Jul 23.
6
Combinations of host biomarkers predict mortality among Ugandan children with severe malaria: a retrospective case-control study.宿主生物标志物的组合预测乌干达重症疟疾儿童的死亡率:一项回顾性病例对照研究。
PLoS One. 2011 Feb 25;6(2):e17440. doi: 10.1371/journal.pone.0017440.
7
Neutrophil gelatinase-associated lipocalin concentrations predict development of acute kidney injury in neonates and children after cardiopulmonary bypass.中性粒细胞明胶酶相关脂质运载蛋白浓度可预测体外循环后新生儿和儿童急性肾损伤的发生。
J Pediatr. 2011 Jun;158(6):1009-1015.e1. doi: 10.1016/j.jpeds.2010.12.057. Epub 2011 Feb 6.
8
The Ngal reporter mouse detects the response of the kidney to injury in real time.Ngal 报告鼠实时检测肾脏对损伤的反应。
Nat Med. 2011 Feb;17(2):216-22. doi: 10.1038/nm.2290. Epub 2011 Jan 16.
9
An update and review of acute kidney injury in pediatrics.儿科急性肾损伤的更新与回顾。
Pediatr Crit Care Med. 2011 May;12(3):339-47. doi: 10.1097/PCC.0b013e3181fe2e0b.
10
Acute kidney injury in childhood: should we be worried about progression to CKD?儿童急性肾损伤:我们是否应担心其进展为慢性肾脏病?
Pediatr Nephrol. 2011 Apr;26(4):509-22. doi: 10.1007/s00467-010-1653-4. Epub 2010 Oct 10.

一项关于尿成纤维细胞生长因子-2 和表皮生长因子作为危重症儿童急性肾损伤潜在生物标志物的初步研究。

A pilot study of urinary fibroblast growth factor-2 and epithelial growth factor as potential biomarkers of acute kidney injury in critically ill children.

机构信息

Division of Pediatric Critical Care, Children's National Medical Center, Washington, DC, USA.

出版信息

Pediatr Nephrol. 2013 Nov;28(11):2189-98. doi: 10.1007/s00467-013-2543-3. Epub 2013 Jul 20.

DOI:10.1007/s00467-013-2543-3
PMID:23872928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4096010/
Abstract

BACKGROUND

Acute kidney injury (AKI) increases the morbidity of critically ill children. Thus, it is necessary to identify better renal biomarkers to follow the outcome of these patients. This prospective case-control study explored the clinical value of a urinary biomarker profile comprised of neutrophil gelatinase lipocalin (uNGAL), fibroblast growth factor-2 (uFGF-2), and epidermal growth factor (uEGF) to follow these patients.

METHODS

Urine samples were collected from 21 healthy children, and 39 critically ill children (mean age 7.5 years ± 6.97 SD) admitted to a pediatric intensive care unit with sepsis or requiring extra corporeal membrane oxygenation (ECMO). uNGAL, uFGF-2, and uEGF levels were measured using ELISA kits during the first 24 h of admission to PICU, at peak of illness, and upon resolution of the critical illness.

RESULTS

On admission, the uNGAL and uFGF-2 levels were increased, and the uEGF levels were decreased, in critically ill children with AKI (n = 19) compared to those without AKI (n = 20), and healthy controls. A biomarker score using the combined cut-off values of uNGAL, uFGF-2, and uEGF (AUC = 0.90) showed the highest specificity to identify children with AKI, relative to each biomarker alone. uNGAL and uFGF-2 on admission showed high sensitivity and specificity to predict mortality (AUC = 0.82).

CONCLUSIONS

The biomarker profile comprised of uNGAL, uFGF-2, and uEGF increased the specificity to detect AKI in critically ill children, when compared to each biomarker used alone. uNGAL and uFGF-2 may also predict the risk of death. Further validation of these findings in a large sample size is warranted.

摘要

背景

急性肾损伤 (AKI) 会增加危重症患儿的发病率。因此,有必要寻找更好的肾脏生物标志物来监测这些患者的预后。本前瞻性病例对照研究探讨了由中性粒细胞明胶酶相关脂质运载蛋白 (uNGAL)、成纤维细胞生长因子-2 (uFGF-2) 和表皮生长因子 (uEGF) 组成的尿生物标志物谱来监测这些患者的临床价值。

方法

收集 21 名健康儿童和 39 名因脓毒症或需要体外膜氧合 (ECMO) 而入住儿科重症监护病房的危重症儿童 (平均年龄 7.5 ± 6.97 岁) 的尿液样本。在入住 PICU 的前 24 小时内、疾病高峰期和危重症缓解时,使用 ELISA 试剂盒测量 uNGAL、uFGF-2 和 uEGF 水平。

结果

在入住时,与无 AKI (n = 20) 和健康对照组相比,AKI (n = 19) 的危重症患儿的 uNGAL 和 uFGF-2 水平升高,uEGF 水平降低。使用 uNGAL、uFGF-2 和 uEGF 的联合截断值的生物标志物评分 (AUC = 0.90) 显示出最高的特异性,可识别出患有 AKI 的儿童,而不是每个生物标志物单独使用。uNGAL 和 uFGF-2 在入院时对预测死亡率具有较高的敏感性和特异性 (AUC = 0.82)。

结论

与单独使用每种生物标志物相比,由 uNGAL、uFGF-2 和 uEGF 组成的生物标志物谱可提高对危重症患儿 AKI 的检测特异性。uNGAL 和 uFGF-2 也可能预测死亡风险。需要在更大的样本量中进一步验证这些发现。