Division of Pediatric Critical Care, Children's National Medical Center, Washington, DC, USA.
Pediatr Nephrol. 2013 Nov;28(11):2189-98. doi: 10.1007/s00467-013-2543-3. Epub 2013 Jul 20.
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.
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.
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).
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.
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。
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。
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)。
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。