Neutrophil gelatinase-associated lipocalin as a biomarker of acute kidney injury: a critical evaluation of current status

被引:195
作者
Haase-Fielitz, Anja [1 ]
Haase, Michael [1 ]
Devarajan, Prasad [2 ]
机构
[1] Univ Magdeburg, Dept Nephrol & Hypertens Diabet & Endocrinol, D-39106 Magdeburg, Germany
[2] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA
关键词
Acute kidney injury; biomarker; lipocalin; DELAYED GRAFT FUNCTION; EARLY URINARY BIOMARKER; CARDIAC-SURGERY; EPITHELIAL-CELLS; ILL CHILDREN; EARLY MARKER; CYSTATIN-C; CARDIOPULMONARY BYPASS; PREDICTIVE BIOMARKERS; RENAL-FUNCTION;
D O I
10.1177/0004563214521795
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background The early prediction of acute kidney injury (AKI) by current clinical and laboratory methods remains inadequate. Neutrophil gelatinase-associated lipocalin (NGAL) has emerged as a promising non-invasive biomarker of kidney injury. We systematically reviewed the utility of plasma and urine NGAL measurements for the prediction of AKI in humans. Methods We searched MEDLINE, PubMed and EMBASE for human biomarker studies that included NGAL (January 2005 to October 2013). Studies reporting on the use of NGAL for the early prediction and prognosis of AKI were analysed in three common clinical settings: cardiac surgery, critical illness and kidney transplantation. Results We identified 58 manuscripts that met our inclusion and exclusion criteria, reporting on more than 16,500 patients. Following cardiac surgery, NGAL measurement in over 7000 patients was predictive of AKI and its severity, with an overall area under the receiver operator characteristic curve (AUC) of 0.82-0.83. Similar results were obtained in over 8500 critically ill patients. In over 1000 patients undergoing kidney transplantation, NGAL measurements predicted delayed graft function with an overall AUC of 0.87. In all three settings, NGAL significantly improved the prediction of AKI risk over the clinical model alone. Conclusions We identified several studies that collectively strongly support the use of NGAL as a biomarker for the prediction of AKI. However, we noted some limitations, including lack of published studies that adhere to diagnostic study guidelines, heterogeneity in AKI definition, the lack of uniformly applicable cut-off values and variability in the performance of commercially available NGAL assays.
引用
收藏
页码:335 / 351
页数:17
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