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临床背景对急性肾损伤生物标志物性能的影响:中性粒细胞明胶酶相关脂质运载蛋白与 L 型脂肪酸结合蛋白的差异。

Impact of clinical context on acute kidney injury biomarker performances: differences between neutrophil gelatinase-associated lipocalin and L-type fatty acid-binding protein.

机构信息

Department of Emergency and Critical Care Medicine, The University of Tokyo, Tokyo, Japan.

Department of Nephrology and Endocrinology, The University of Tokyo, Tokyo, Japan.

出版信息

Sci Rep. 2016 Sep 8;6:33077. doi: 10.1038/srep33077.

Abstract

Application of acute kidney injury (AKI) biomarkers with consideration of nonrenal conditions and systemic severity has not been sufficiently determined. Herein, urinary neutrophil gelatinase-associated lipocalin (NGAL), L-type fatty acid-binding protein (L-FABP) and nonrenal disorders, including inflammation, hypoperfusion and liver dysfunction, were evaluated in 249 critically ill patients treated at our intensive care unit. Distinct characteristics of NGAL and L-FABP were revealed using principal component analysis: NGAL showed linear correlations with inflammatory markers (white blood cell count and C-reactive protein), whereas L-FABP showed linear correlations with hypoperfusion and hepatic injury markers (lactate, liver transaminases and bilirubin). We thus developed a new algorithm by combining urinary NGAL and L-FABP with stratification by the Acute Physiology and Chronic Health Evaluation score, presence of sepsis and blood lactate levels to improve their AKI predictive performance, which showed a significantly better area under the receiver operating characteristic curve [AUC-ROC 0.940; 95% confidential interval (CI) 0.793-0.985] than that under NGAL alone (AUC-ROC 0.858, 95% CI 0.741-0.927, P = 0.03) or L-FABP alone (AUC-ROC 0.837, 95% CI 0.697-0.920, P = 0.007) and indicated that nonrenal conditions and systemic severity should be considered for improved AKI prediction by NGAL and L-FABP as biomarkers.

摘要

急性肾损伤(AKI)标志物的应用,考虑到非肾脏情况和全身严重程度,尚未得到充分确定。在此,我们评估了在我院重症监护病房治疗的 249 例危重症患者的尿中性粒细胞明胶酶相关脂质运载蛋白(NGAL)、L 型脂肪酸结合蛋白(L-FABP)和非肾脏疾病,包括炎症、低灌注和肝功能障碍。主成分分析显示 NGAL 和 L-FABP 具有不同的特征:NGAL 与炎症标志物(白细胞计数和 C 反应蛋白)呈线性相关,而 L-FABP 与低灌注和肝损伤标志物(乳酸、肝转氨酶和胆红素)呈线性相关。因此,我们通过结合尿 NGAL 和 L-FABP 并根据急性生理学和慢性健康评估评分、脓毒症和血乳酸水平进行分层,开发了一种新的算法,以提高其 AKI 预测性能,该算法的受试者工作特征曲线下面积 [AUC-ROC 0.940;95%置信区间(CI)0.793-0.985] 明显优于单独使用 NGAL (AUC-ROC 0.858,95%CI 0.741-0.927,P=0.03)或单独使用 L-FABP(AUC-ROC 0.837,95%CI 0.697-0.920,P=0.007),表明非肾脏情况和全身严重程度应考虑用于改善 NGAL 和 L-FABP 作为生物标志物的 AKI 预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39a7/5015077/db7d47caf437/srep33077-f1.jpg

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