Sensitivity and specificity of a single emergency department measurement of urinary neutrophil gelatinase-associated lipocalin for diagnosing acute kidney injury

被引:515
作者
Nickolas, Thomas L.
O'Rourke, Matthew J.
Yang, Jun
Sise, Meghan E.
Canetta, Pietro A.
Barasch, Nicholas
Buchen, Charles
Khan, Faris
Mori, Kiyoshi
Gigllo, James
Devarajan, Prasad
Barasch, Jonathan
机构
[1] Columbia University, PH 4 Stem, New York, NY 10032
[2] Department of Medicine, Columbia University, New York, NY 10032
[3] College of Physicians and Surgeons, Columbia University Medical School, New York, NY 10032
[4] Saint Luke's Roosevelt Hospital, Columbia University, New York, NY 10019
[5] Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Sakyo-ku hio 45229-3039, Kyoto 606-8507
[6] Department of Emergency Medicine, Columbia University, New York, NY 10032
[7] Section of Nephrology, Cincinnati Children's Hospital, University of Cincinnati, Cincinnati, OH 45229-3039
关键词
D O I
10.7326/0003-4819-148-11-200806030-00003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: A single serum creatinine measurement cannot distinguish acute kidney injury from chronic kidney disease or prerenal azotemia. Objective: To test the sensitivity and specificity of a single measurement of urinary neutrophil gelatinase-associated lipocalin (NGAL) and other urinary proteins to detect acute kidney injury in a spectrum of patients. Design: Prospective cohort study. Setting: Emergency department of Columbia University Medical Center, New York, New York. Participants: 635 patients admitted to the hospital with acute kidney injury, prerenal azotemia, chronic kidney disease, or normal kidney function. Measurements: Diagnosis of acute kidney injury was based on the RIFLE (risk, injury, failure, loss, and end-stage) criteria and assigned by researchers who were blinded to experimental measurements. Urinary NGAL was measured by immunoblot, N-acetyl-beta-D-glucosaminidase (NAG) by enzyme measurement, alpha(1)-microglobulin and alpha(1)-acid glycoprotein by immunonephelometry, and serum creatinine by Jaffe kinetic reaction. Experimental measurements were not available to treating physicians. Results: Patients with acute kidney injury had a significantly elevated mean urinary NGAL level compared with the other kidney function groups (416 mu g/g creatinine [SD, 387]; P = 0.001). At a cutoff value of 130 mu g/g creatinine, sensitivity and specificity of NGAL for detecting acute injury were 0.900 (95% CI, 0.73 to 0.98) and 0.995 (CI, 0.990 to 1.00), respectively, and positive and negative likelihood ratios were 181.5 (CI, 58.33 to 564.71) and 0.10 (CI, 0.03 to 0.29); these values were superior to those for NAG, alpha(1)-microglobulin, alpha(1)-acid glycoprotein, fractional excretion of sodium, and serum creatinine. In multiple logistic regression, urinary NGAL level was highly predictive of clinical outcomes, including nephrology consultation, dialysis, and admission to the intensive care unit (odds ratio, 24.71 [CI, 7.69 to 79.42]). Limitations: All patients came from a single center. Few kidney biopsies were performed. Conclusion: A single measurement of urinary NGAL helps to distinguish acute injury from normal function, prerenal azotemia, and chronic kidney disease and predicts poor inpatient outcomes.
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页码:810 / U21
页数:11
相关论文
共 52 条
[1]  
Åhlström A, 2004, CLIN NEPHROL, V62, P344
[2]  
[Anonymous], 2011, Categorical data analysis
[3]   Acute renal failure - definition, outcome measures, animal models, fluid therapy and information technology needs: the Second International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) Group [J].
Bellomo, R ;
Ronco, C ;
Kellum, JA ;
Mehta, RL ;
Palevsky, P .
CRITICAL CARE, 2004, 8 (04) :R204-R212
[4]   Lipocalin 2-deficient mice exhibit increased sensitivity to Escherichia coli infection but not to ischemia-reperfusion injury [J].
Berger, T ;
Togawa, A ;
Duncan, GS ;
Elia, AJ ;
You-Ten, A ;
Wakeham, A ;
Fong, HEH ;
Cheung, CC ;
Mak, TW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (06) :1834-1839
[5]   Recent advances in the pathophysiology of ischemic acute renal failure [J].
Bonventre, JV ;
Weinberg, JM .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (08) :2199-2210
[6]   Acute renal failure in intensive care units - Causes, outcome, and prognostic factors of hospital mortality: A prospective, multicenter study [J].
Brivet, FG ;
Kleinknecht, DJ ;
Loirat, P ;
Landais, PJM ;
Bedock, B ;
Bleichner, G ;
Richard, C ;
Coste, F ;
BrunBuisson, C ;
Sicot, C ;
Tenaillon, A ;
Gajdos, P ;
Blin, F ;
Saulnier, F ;
Agostini, MM ;
Nicolas, F ;
FeryLemonnier, E ;
Staikowski, F ;
Carlet, J ;
Guivarch, G ;
Fraisse, F ;
Ricome, J ;
Tempe, JD ;
Mezzarobba, P .
CRITICAL CARE MEDICINE, 1996, 24 (02) :192-198
[7]   MOLECULAR-CLONING AND EXPRESSION OF A CDNA-ENCODING NGAL - A LIPOCALIN EXPRESSED IN HUMAN NEUTROPHILS [J].
BUNDGAARD, JR ;
SENGELOV, H ;
BORREGAARD, N ;
KJELDSEN, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 202 (03) :1468-1475
[8]   Acute kidney injury, mortality, length of stay, and costs in hospitalized patients [J].
Chertow, GM ;
Burdick, E ;
Honour, M ;
Bonventre, JV ;
Bates, DW .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (11) :3365-3370
[9]   PROGNOSTIC STRATIFICATION IN CRITICALLY ILL PATIENTS WITH ACUTE-RENAL-FAILURE REQUIRING DIALYSIS [J].
CHERTOW, GM ;
CHRISTIANSEN, CL ;
CLEARY, PD ;
MUNRO, C ;
LAZARUS, JM .
ARCHIVES OF INTERNAL MEDICINE, 1995, 155 (14) :1505-1511
[10]   Exogenous alpha-1-acid glycoprotein protects against renal ischemia-reperfusion injury by inhibition of inflammation and apoptosis [J].
de Vries, B ;
Walter, SJ ;
Wolfs, TGAM ;
Hochepied, T ;
Räbinä, J ;
Heeringa, P ;
Parkkinen, J ;
Libert, C ;
Buurman, WA .
TRANSPLANTATION, 2004, 78 (08) :1116-1124