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Volume 54, Issue 6, Pages 1012-1024 (December 2009)


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Accuracy of Neutrophil Gelatinase-Associated Lipocalin (NGAL) in Diagnosis and Prognosis in Acute Kidney Injury: A Systematic Review and Meta-analysis

NGAL Meta-analysis Investigator GroupMichael Haase, MD1Corresponding Author Informationemail address, Rinaldo Bellomo, MD2, Prasad Devarajan, MD3, Peter Schlattmann, MD, MSc4, Anja Haase-Fielitz, PharmD1

Received 15 April 2009; accepted 27 July 2009. published online 22 October 2009.

Refers to article:
Testing New Biomarkers for Acute Kidney Injury: Association, Prediction, and Intervention
Chirag R. Parikh, Amit X. Garg
American Journal of Kidney Diseases
December 2009 (Vol. 54, Issue 6, Pages 987-989)
Full Text | Full-Text PDF (138 KB)
Background

Neutrophil gelatinase-associated lipocalin (NGAL) appears to be a promising biomarker for the early diagnosis of acute kidney injury (AKI); however, a wide range in its predictive value has been reported.

Study Design

Meta-analysis of diagnostic test studies using custom-made standardized data sheets sent to each author.

Setting & Population

Different clinical settings of AKI.

Selection Criteria for Studies

MEDLINE, EMBASE, and CENTRAL databases and congress abstracts were searched for studies reporting the value of NGAL to predict AKI.

Index Tests

Plasma/serum and urine NGAL within 6 hours from the time of insult (if known) or 24-48 hours before the diagnosis of AKI if the time of insult was not known.

Reference Tests

The primary outcome was AKI, defined as an increase in serum creatinine level > 50% from baseline within 7 days or contrast-induced nephropathy (creatinine increase > 25% or concentration > 0.5 mg/dL in adults or > 50% increase in children within 48 hours). Other outcomes predicted using NGAL were renal replacement therapy initiation and in-hospital mortality.

Results

Using a hierarchical bivariate generalized linear model to calculate the diagnostic odds ratio (DOR) and sample size–weighted area under the curve for the receiver-operating characteristic (AUC-ROC), we analyzed data from 19 studies and 8 countries involving 2,538 patients, of whom 487 (19.2%) developed AKI. Overall, the DOR/AUC-ROC of NGAL to predict AKI was 18.6 (95% CI, 9.0-38.1)/0.815 (95% CI, 0.732-0.892). The DOR/AUC-ROC when standardized platforms were used was 25.5 (95% CI, 8.9-72.8)/0.830 (95% CI, 0.741-0.918) with a cutoff value > 150 ng/mL for AKI compared with 16.7 (95% CI, 7.1-39.7)/0.732 (95% CI, 0.656-0.830) for “research-based” NGAL assays. In cardiac surgery patients, the DOR/AUC-ROC of NGAL was 13.1 (95% CI, 5.7-34.8)/0.775 (95% CI, 0.669-0.867); in critically ill patients, 10.0 (95% CI, 3.0-33.1)/0.728 (95% CI, 0.615-0.834); and after contrast infusion, 92.0 (95% CI, 10.7-794.1)/0.894 (95% CI, 0.826-0.950). The diagnostic accuracy of plasma/serum NGAL (17.9 [95% CI, 6.0-53.7]/0.775 [95% CI, 0.679-0.869]) was similar to that of urine NGAL (18.6 [95% CI, 7.2-48.4]/0.837 [95% CI, 0.762-0.906]). We identified age to be an effective modifier of NGAL value with better predictive ability in children (25.4 [95% CI, 8.9-72.2]/0.930 [95% CI, 0.883-0.968]) compared with adults (10.6 [95% CI, 4.8-23.4]/0.782 [95% CI, 0.689-0.872]). NGAL level was a useful prognostic tool with regard to the prediction of renal replacement therapy initiation (12.9 [95% CI, 4.9-33.9]/0.782 [95% CI, 0.648-0.917]) and in-hospital mortality (8.8 [95% CI, 1.9-40.8]/0.706 [95% CI, 0.530-0.747]).

Limitations

Serum creatinine level was used for AKI definition.

Conclusions

NGAL level appears to be of diagnostic and prognostic value for AKI.

1 Department of Nephrology and Intensive Care Medicine, Charité University Medicine, Berlin, Germany

2 Department of Intensive Care, Austin Health, Melbourne, Australia

3 Department of Pediatrics and Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

4 Department of Biometry and Clinical Epidemiology, Charité University Medicine, Campus Mitte, Berlin, Germany

Corresponding Author InformationAddress correspondence to Michael Haase, MD, Department of Nephrology and Intensive Care Medicine, Charité-University Medicine Berlin, Campus Virchow-Klinikum, 13353 Berlin, Germany

 Originally published online as doi:10.1053/j.ajkd.2009.07.020 on October 22, 2009.

 Members of the NGAL Meta-analysis Investigator Group are listed at the end of this article.

PII: S0272-6386(09)01075-0

doi:10.1053/j.ajkd.2009.07.020


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