Plasma neutrophil gelatinase-associated lipocalin for the prediction of acute kidney injury in acute heart failure
© Breidthardt et al.; licensee BioMed Central Ltd. 2012
Received: 20 June 2011
Accepted: 7 January 2012
Published: 7 January 2012
The accurate prediction of acute kidney injury (AKI) in patients with acute heart failure (AHF) is an unmet clinical need. Neutrophil gelatinase-associated lipocalin (NGAL) is a novel sensitive and specific marker of AKI.
A total of 207 consecutive patients presenting to the emergency department with AHF were enrolled. Plasma NGAL was measured in a blinded fashion at presentation and serially thereafter. The potential of plasma NGAL levels to predict AKI was assessed as the primary endpoint. We defined AKI according to the AKI Network classification.
Overall 60 patients (29%) experienced AKI. These patients were more likely to suffer from pre-existing chronic cardiac or kidney disease. At presentation, creatinine (median 140 (interquartile range (IQR), 91 to 203) umol/L versus 97 (76 to 132) umol/L, P < 0.01) and NGAL (114.5 (IQR, 67.1 to 201.5) ng/ml versus 74.5 (60 to 113.9) ng/ml, P < 0.01) levels were significantly higher in AKI compared to non-AKI patients. The prognostic accuracy for measurements obtained at presentation, as quantified by the area under the receiver operating characteristic curve was mediocre and comparable for the two markers (creatinine 0.69; 95%CI 0.59 to 0.79 versus NGAL 0.67; 95%CI 0.57 to 0.77). Serial measurements of NGAL did not further increase the prognostic accuracy for AKI. Creatinine, but not NGAL, remained an independent predictor of AKI (hazard ratio (HR) 1.12; 95%CI 1.00 to 1.25; P = 0.04) in multivariable regression analysis.
Plasma NGAL levels do not adequately predict AKI in patients with AHF.
Acute kidney injury (AKI) is an increasingly common complication in hospitalized patients. Over the last decade the incidence of AKI has steadily increased . Current estimates assume that annually about 17 million hospital admissions in the United States are complicated by AKI, resulting in additional health care costs of 10 billion dollars .
AKI occurring during acute heart failure (AHF) has been termed the cardiorenal syndrome Type I . AHF patients developing AKI have been shown to have increased morbidity, mortality and treatment costs [4, 5]. Unfortunately, the accurate prediction of AKI is an unmet clinical need .
Neutrophil gelatinase-associated lipocalin (NGAL; also known as human neutrophil lipocalin, lipocalin-2, siderocalin, 24p3, or LCN2) is a small molecule that belongs to the well-defined superfamily of proteins called lipocalins . Human NGAL was originally identified as a 25-kDa protein associated with purified gelatinase obtained from the supernatant of activated neutrophils, which normally are the main cellular source of circulating NGAL . Subsequent studies have identified tubularly secreted NGAL as a novel and specific biomarker for the early detection of AKI in several settings including cardiac surgery [8, 9], contrast agent administration [10, 11], unselected patients in the emergency department  and in critically ill patients [13–15].
As the main pathophysiological mechanisms of AKI in AHF as well as the timing of insults may differ from the settings mentioned above, it is unknown whether these promising initial findings can be extrapolated to AHF. Therefore, we aimed to examine NGAL levels in the prediction of AKI in patients with AHF.
Materials and methods
Setting and study population
This prospective study investigated the potential of plasma NGAL levels to predict the occurrence of AKI and worsening renal function (WRF) in consecutive AHF patients presenting to the participating emergency departments (University Hospital Basel, Kantonsspital Aarau, and Kantonsspital Luzern) from April 2006 to August 2009. To be eligible for enrollment, patients had to be over 18 years old and present with symptoms and signs of AHF. AHF was diagnosed and patients were treated according to current European Society of Cardiology (ESC) guidelines . Patients undergoing chronic hemodialysis were excluded. There were no other excluding factors that may have omitted patients with renal disease or biased their enrollment in the trial. AKI and WRF diagnoses could not be determined in four patients, who were treated in the emergency department on an outpatient basis only and for whom only one serum creatinine draw and no preadmission serum creatinine values were available. These patients were excluded from the analysis. The study was carried out according to the principles of the Declaration of Helsinki. It was approved by the local ethical committee (Ethikkomission beider Basel, Reference-Number: EK 52/06). Written informed consent was obtained from all participants.
Clinical evaluation and biomarker measurements
At the time of enrollment all patients underwent an initial clinical assessment including clinical history, physical examination, pulse oximetry, blood tests including B-type natriuretic peptide (BNP), and chest X-ray. Echocardiography, blood gas analyses and cardiac magnetic resonance imaging (MRI) were performed according to the treating physicians' recommendations. Creatinine levels were measured at presentation to the emergency department, daily for the next four days and at discharge from the hospital. Blood samples for determination of NGAL were collected at presentation, in six-hour intervals during the first 24 hours as well as after 36 hours and 48 hours. After centrifugation, samples were frozen at -80°C until assayed in a blinded fashion in a single batch using a fluorescence- immunoassay (Triage ® NGAL; Alere San Diego Incorporated; San Diego, CA, USA). According to Alere the lower detection limit of the assay is 45 ng/ml, the upper detection limit is 1,310 ng/ml. The product package insert describes the lot to lot coefficient of variance as 6.4%, 5.8%, and 3.9% for low, medium, and high NGAL values, respectively. The 95th percentile in 120 healthy individuals between 18 and 83 years old was 159 ng/ml. All investigated cardiovascular drugs tested at concentrations representing at least two times the maximal therapeutic dose, did not show crossreactivity or interference with the assay.
The potential of plasma NGAL levels to predict the occurrence of AKI during the first four days was assessed as the primary endpoint. We defined and graded AKI according to the Acute Kidney Injury Network (AKIN) classification as a new-onset increase in serum creatinine ≥ 0.3 mg/dl (26.4 mmol/l) over stable baseline creatinine values . AKI stage 1 included acute creatinine increases between ≥ 0.3 mg/dl (≥ 26.4 μmol/l) and up to 200% over stable baseline creatinine, while increases in serum creatinine between > 200% to 300% from stable baseline were considered stage 2. AKI stage 3 entailed acute increases of serum creatinine to more than 300% (> 3-fold) as well as serum creatinine values ≥ 354 μmol/l showing an acute increase of at least 0.5 mg/dl (44 μmol/l]) . We determined baseline kidney function for 189 (91%) patients by analysis of serum creatinine and medical history using the electronic medical records for the six months prior the index hospitalization. Baseline creatinine was defined as the lowest creatinine value obtained by the individual patient during the observational period. In the absence of pre-admission data the lowest creatinine value measured during the index hospitalization was accepted as the presumptive baseline value.
The statistical analyses were performed using the SPSS/PC (version 19.0,
SPSS Inc., USA) and the R-project (online at http://www.R-project.org) software packages. A statistical significance level of 0.05 was used. Discrete variables are expressed as counts (percentage) and continuous variables as means ± standard deviation (SD) or median and interquartile range [IQR], unless stated otherwise. The comparison between the two groups was done with the chi-square test and Fisher exact test for categorical variables and t-test for continuous variables if normally distributed or Mann-Whitney test if not normally distributed. The variation between the two groups of NGAL values was compared using the Kruskall-Wallis test, Mann-Whitney test and two-way analysis of variance (ANOVA) for repeated measurements. Comparisons between NGAL values at various time points for individual patients were done using Wilcoxon test. The Spearman rank correlation was used to perform correlation analyses. All hypothesis testing was two-tailed.
The prognostic accuracy of the different models was evaluated using receiver operating characteristic (ROC) curve analysis. Areas under ROC curves were compared using MedCalc software (version 9.2., MedCalc Software, Mariakerke, Belgium). Univariate and multivariate binary regression analysis was applied to identify predictors of AKI and WRF. Overall 37 candidate variables were assessed in univariate regression analysis. The variable inclusion method was used for multivariate regression analysis. Multivariate analysis included all significant candidate variables (P < 0.05) established in univariate analysis. To limit the effects of co-linearity between multiple variables of renal impairment a simplified multivariate analysis was also conducted. The Hosmer-Lemeshow test was conducted to compare the observed and expected frequencies of AKI and WRF based on the values of the estimated probabilities obtained by logistic regression analysis.
Baseline Characteristics of 207 patients
Total number of patients
Coronary artery disease
Chronic kidney disease
Long term medication use
Renin Angiotensin System-Blockers
Blood pressure (mmHg)
Heart rate (per minute)
Respiratory rate (per minute)
Oxygen saturation (%)
Body Mass Index (kg/m2)
Noninvasive CVP (cmH20)
LV ejection fraction (%)
C-reactive protein (mg/l)
Uric acid (mmol/l)
Baseline eGFR (ml/min)*
Troponin T (ug/l)
0.01 [0.01- 0.30]
Plasma NGAL levels in patients experiencing acute kidney injury
Of note, in the 108 patients presenting with creatinine levels within the normal range (< 110 mmol/l) no differences in NGAL levels could be observed between AKI and non-AKI patients (median NGAL 60 ng/ml versus 65 ng/ml; P = 0.40).
Importantly, in an ANOVA 2-way analysis for repeated measurements neither a change of NGAL values over time (P = 0.66), nor a significant difference between the NGAL levels of patients experiencing AKI and those not experiencing AKI could be detected (P = 0.25).
Plasma NGAL as a predictor of acute kidney injury
In patients presenting with creatinine levels within the normal range, the AUC for the prediction of AKI was poor and comparable for both markers (creatinine: 0.51 versus NGAL 0.52). Furthermore, the potential of the two markers to detect advanced AKI (stage 3) (AUC creatinine: 0.94 versus AUC NGAL 0.88) was similar.
Prediction of the occurrence of acute kidney injury in univariate and multivariate regression analysis Univariate analysis
HR 1.03 (95%CI 0.99-1.06)
Hx Heart Failure
HR 2.02 (95%CI 1.08-3.81)
Hx Chronic Kidney Disease
HR 2.15 (95%CI 1.16-3.99)
Steady State Creatinine > 110 μol/l
HR 2.21 (95%CI 1.16-4.23)
Outpatient Diuretic Treatment
HR 2.36 (95%CI 1.03-5.41)
Systolic Blood Pressure (mmHg)
HR 0.99 (95%CI 0.97-0.99)
Loop Diuretic Dose during first 72h
HR 1.00 (95%CI 1.00-1.01)
HR 1.09 (95%CI 1.04-1.15)
Uric Acid (mmol/l)
HR 1.00 (95%Ci 1.00-1.00)
C-reactive protein (mg/l)
HR 1.01 (95%CI 1.00-1.01)
Troponin T (ug/l)
HR 1.06 (95%CI 1.01-1.19)
B-type natriuretic peptide (pg/ml)
(for every increase of 100 pg/ml)
HR1.00 (95%CI 0.99-1.02)
LV ejection fraction (%)
HR 0.99 (95%CI 0.97-1.02)
(for every increase of 10 mml/l)
HR 1.13 (95%CI 1.01-1.20)
(for every increase of 10 ng/ml)
HR 1.01 (95%CI 1.04-1.15)
NGAL > 94 ng/ml
HR 1.44 (96%CI 0.15-14.20)
NGAL > 140 ng/ml
HR 3.40 (95%CI 1.61-7.15)
Hx Heart Failure
HR 1.75 (95%CI 0.64-4.80)
Steady State Creatinine > 110 μmol/l
HR 2.41 (95%CI 0.66-8.88)
Systolic Blood Pressure (mmHg)
HR 1.01 (95%CI 0.99-1.02)
Outpatient Diuretic Treatment
HR 1.25 (95%CI 0.32-4.02)
Loop Diuretic Dose during first 72h
HR 1.00 (95%CI 0.99-1.00)
C-reactive protein (mg/l)
HR 1.00 (95%CI 0.99-1.01)
Troponin T (ug/l)
HR 3.72 (95%CI 0.02-13.53)
(for every increase of 10 mml/l)
HR 1.12 (95%CI 1.00-1.24)
(for every increase of 10 ng/ml)
HR 1.05 (95%CI 0.98-1.13)
During serial sampling no significant changes in plasma NGAL levels were observed in the 41 patients experiencing AKI after presentation. Hence, NGAL changes over the first 24 hours did not provide additional predictive information.
Plasma NGAL as a predictor of in-hospital worsening renal function
In this investigation we examined the potential of plasma NGAL levels at admission and serially thereafter to predict the occurrence of AKI and WRF in 207 patients with AHF. There are several key findings in this study. First, in AHF patients, plasma NGAL levels are significantly correlated to renal indices at presentation but also to age and baseline renal function. However, plasma NGAL levels are not associated with the extent of hemodynamic cardiac stress as quantified by BNP, the extent of venous congestion or inflammation. Second and most importantly, we found that spot measurements of plasma NGAL at presentation failed to improve the prediction of AKI over creatinine measurement. While both markers were significantly higher in patients experiencing AKI, their accuracy for the prediction of AKI was only modest. Third, the combination of plasma NGAL levels and creatinine did not result in a higher accuracy than creatinine alone. Fourth, the accuracy of plasma NGAL was even lower in patients presenting with creatinine values within the normal range. Fifth, plasma NGAL levels did not show a clear trend preceding the occurrence of AKI. Consequently, serial measurements did not add to the diagnostic potential of plasma NGAL at presentation.
Our results represent the first larger scale study investigating the potential of plasma NGAL in the setting of AHF. The results of an earlier study enrolling 91 patients with AHF support our observations. Aghel and colleagues also found spot measurements of serum NGAL to be significantly higher in patients experiencing early AKI . Furthermore, their study described comparable AUCs for serum NGAL and estimated glomerular filtration rate (eGFR) for the prediction of early AKI (0.7 and 0.61, respectively). Unfortunately, due to the small number of patients in their study no extensive multivariate analysis could be performed. Contrastingly, a very recent study by Alvelos and co-workers found spot measurements of NGAL to powerfully predict AKI in 114 hospitalized AHF patients (AUC 0.93). However, their study differs significantly from the present study and also the work presented by Aghel, since it selectively assessed the predictive potential of NGAL levels drawn on the first in-hospital day and only considered AKI occurring between day two and day three. Applying these criteria to our population led to the exclusion of 24 (40%) early AKI cases, explaining the lower incidence of AKI occurring in the Alvelos study (12% versus 29%). Additionally, using the Alvelos definition of early AKI in a secondary analysis, we found the predictive accuracy of NGAL levels at presentation to be comparable to our primary analysis (AUC 0.61) and were therefore not able to confirm their findings. It can only be speculated that the narrower and sub-acute observational period in the Alvelos study reflects a more specific, NGAL-detectable AKI pathology, while the more inclusive observational period in this study might cover a wider range of AKI triggers.
The results obtained for AHF patients differ from the results obtained in other clinical settings, such as after cardiac surgery [8, 9] and contrast agent administration [10, 11], in which NGAL was established as a promising early marker of AKI. However, contrast-induced nephropathy and post-surgical AKI are marked by a clear time of injury. In these settings NGAL has repeatedly been proven to increase significantly three to four hours after the insult, while creatinine only increases 48 to 72 hours later. In contrast, the pathophysiological mechanisms underlying renal dysfunction in patients with AHF appear to be multifactorial and not well defined. Overall, an imbalance between the failing heart, the neurohumoral system and inflammatory responses has been associated with the occurrence of renal dysfunction . Additionally, hemodynamic factors including the adequacy of renal perfusion  and the degree of venous congestion [22, 23] as well as drug nephrotoxicity appear to contribute to the development of AKI in AHF. Hence, AKI in AHF might well be caused by serial insults making its prediction especially difficult. Similarly, two studies directly comparing the predictive potential of admission NGAL to admission creatinine  or clinical prediction models  in critically ill patients, found classical predictors of AKI to at least equal if not surpass the potential of NGAL. Hence, even in the setting of critically ill patients, NGAL levels might not be able to act as a stand-alone test [24, 25].
The significant correlation of admission NGAL levels with baseline creatinine levels observed in this study and the correlation of urinary NGAL levels with renal indices in stable chronic heart failure [26, 27] suggest that NGAL levels in AHF may reflect chronic structural tubular damage. This thesis is further supported by the stable NGAL levels over time in patients experiencing AKI in this study. A chronic structural tubular damage and persistently elevated NGAL levels appear to be widespread in the setting of heart failure  and elevated NGAL levels have been associated with increased short-term mortality [28, 29]. Consequently, the dampened kinetics of NGAL levels before the occurrence of AKI might contribute to the limited predictive potential of plasma NGAL in AHF.
Additionally, recent studies found circulating NGAL levels to be influenced by various extra-renal factors . Systemically elevated NGAL levels have been observed in infectious diseases , primary and secondary anemia , various human cancers  and animal models of obesity . In the setting of cardiovascular diseases, elevated NGAL levels were found in coronary plaques, the failing myocardium and in the circulation of heart failure patients . The combined influence of this systemic NGAL pool might contribute to the limited predictive potential of plasma NGAL in AHF. The predictive potential of urinary NGAL, which appears to be less impacted by extra-renal factors, has not been selectively examined in AHF patients yet. However, a recent meta-analysis including patients from 19 studies showed comparable performances for plasma and urinary NGAL .
Potential limitations of the current study merit consideration. First, only Swiss centers participated in this study. However as baseline characteristics, treatment and the frequency of AKI rates were similar to those observed in large registry studies, we consider our results representative. Second, we did not include the urine output criteria of the AKIN classification into the definition and grading of AKI, as loop diuretics impacting urine were used in the majority of our patients and adequate urine output collection is especially difficult during the early in-hospital period marked by repeated changes of the care-team. However, these difficulties are shared by previously published studies assessing the predictive potential of NGAL in the non-ICU setting, which also opted to exclude the urine output criteria for AKI diagnosis [12, 18, 19]. Third, we cannot differentiate between 'pre-renal' and 'structural" disturbances of kidney function as the reason for AKI. However, independent of the underlying pathology, minor changes of renal function have repeatedly been associated with a worse patient outcome [35, 36]. We therefore believe that adequate prediction of AKI in AHF should be able to foresee these prognostically important creatinine changes. Fourth, the definition of AKI is based on serial measurements of serum creatinine, hence an incorporation bias [37, 38] might have favored presentation values of serum creatinine in predicting AKI in ROC curve and regression analyses. However, in the absence of a non-creatinine based definition of AKI, we feel that to provide tangible clinical benefit plasma NGAL would have to improve the early detection of AKI over the current gold standard. Finally, clinical parameters (most importantly chronic kidney disease) previously shown to predict in-hospital AKI (observational period presentation to discharge) [6, 39, 40] failed to independently predict early AKI in this study. These differences most likely represent the increased importance of acute parameters (serum creatinine incorporating community acquired AKI and chronic kidney disease) versus chronic parameters (chronic kidney disease, outpatient diuretic therapy) in the prediction of early versus late AKI. Nevertheless, these clinical parameters remained non-significantly associated with an increased occurrence of early AKI.
Plasma NGAL levels do not adequately predict AKI and WRF in patients with AHF. This lack of predictive power is probably caused by the multifactorial pathomechanism underlying the cardiorenal syndrome and chronically elevated NGAL levels caused by chronic tubular injury and extrarenal NGAL production in heart failure patients.
Spot measurements of plasma NGAL at presentation do not improve the prediction of AKI over creatinine in patients with acute heart failure.
The combination of plasma NGAL levels and creatinine does not result in a higher predictive accuracy than creatinine alone.
In acute heart failure plasma NGAL levels do not show a clear trend preceding the occurrence of AKI.
Consequently, serial measurements do not add to the predictive potential of plasma NGAL at presentation.
acute heart failure
acute kidney injury
Acute Kidney Injury Network
area under the curve
analysis of variance
B-type natriuretic peptide
estimated glomerular filtration rate
magnetic resonance imaging
neutrophil gelatinase-associated lipocalin
receiver operating characteristic
worsening renal function
We are indebted to the patients who participated in the study and to the Emergency Department staff as well as the laboratory technicians for their most valuable efforts. Furthermore, the authors thank Dr. Etienne Gayat, Hôpital Lariboisière APHP; University Paris for his statistical support. This study was supported by research grants from the University of Basel (to Dr. Breidthardt), the Swiss National Science Foundation (to Dr. Mueller), and ALERE. The funding bodies had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
- Hsu CY, McCulloch CE, Fan D, Ordonez JD, Chertow GM, Go AS: Community-based incidence of acute renal failure. Kidney Int 2007, 72: 208-212. 10.1038/sj.ki.5002297PubMed CentralView ArticlePubMedGoogle Scholar
- Chertow GM, Burdick E, Honour M, Bonventre JV, Bates DW: Acute kidney injury, mortality, length of stay, and costs in hospitalized patients. J Am Soc Nephrol 2005, 16: 3365-3370. 10.1681/ASN.2004090740View ArticlePubMedGoogle Scholar
- Ronco C, McCullough P, Anker SD, Anand I, Aspromonte N, Bagshaw SM, Bellomo R, Berl T, Bobek I, Cruz DN, Daliento L, Davenport A, Haapio M, Hillege H, House AA, Katz N, Maisel A, Mankad S, Zanco P, Mebazaa A, Palazzuoli A, Ronco F, Shaw A, Sheinfeld G, Soni S, Vescovo G, Zamperetti N, Ponikowski P, Acute Dialysis Quality Initiative (ADQI) consensus group: Cardio-renal syndromes: report from the consensus conference of the acute dialysis quality initiative. Eur Heart J 2010, 31: 703-711. 10.1093/eurheartj/ehp507PubMed CentralView ArticlePubMedGoogle Scholar
- Hata N, Yokoyama S, Shinada T, Kobayashi N, Shirakabe A, Tomita K, Kitamura M, Kurihara O, Takahashi Y: Acute kidney injury and outcomes in acute decompensated heart failure: evaluation of the RIFLE criteria in an acutely ill heart failure population. Eur J Heart Fail 2010, 12: 32-37. 10.1093/eurjhf/hfp169View ArticlePubMedGoogle Scholar
- Damman K, Navis G, Voors AA, Asselbergs FW, Smilde TD, Cleland JG, van Veldhuisen DJ, Hillege HL: Worsening renal function and prognosis in heart failure: systematic review and meta-analysis. J Card Fail 2007, 13: 599-608. 10.1016/j.cardfail.2007.04.008View ArticlePubMedGoogle Scholar
- Breidthardt T, Socrates T, Noveanu M, Klima T, Heinisch C, Reichlin T, Potocki M, Nowak A, Tschung C, Arenja N, Bingisser R, Mueller C: Effect and Clinical Prediction of Worsening Renal Function in Acute Decompensated Heart Failure. Am J Cardiol 2011, 107: 730-735. 10.1016/j.amjcard.2010.10.056View ArticlePubMedGoogle Scholar
- Bolignano D, Donato V, Coppolino G, Campo S, Buemi A, Lacquaniti A, Buemi M: Neutrophil gelatinase-associated lipocalin (NGAL) as a marker of kidney damage. Am J Kidney Dis 2008, 52: 595-605. 10.1053/j.ajkd.2008.01.020View ArticlePubMedGoogle Scholar
- Wagener G, Jan M, Kim M, Mori K, Barasch JM, Sladen RN, Lee HT: Association between increases in urinary neutrophil gelatinase-associated lipocalin and acute renal dysfunction after adult cardiac surgery. Anesthesiology 2006, 105: 485-491. 10.1097/00000542-200609000-00011View ArticlePubMedGoogle Scholar
- Mishra J, Dent C, Tarabishi R, Mitsnefes MM, Ma Q, Kelly C, Ruff SM, Zahedi K, Shao M, Bean J, Mori K, Barasch J, Devarajan P: Neutrophil gelatinase-associated lipocalin (NGAL) as a biomarker for acute renal injury after cardiac surgery. Lancet 2005, 365: 1231-1238. 10.1016/S0140-6736(05)74811-XView ArticlePubMedGoogle Scholar
- Bachorzewska-Gajewska H, Malyszko J, Sitniewska E, Malyszko JS, Dobrzycki S: Neutrophil-gelatinase-associated lipocalin and renal function after percutaneous coronary interventions. Am J Nephrol 2006, 26: 287-292. 10.1159/000093961View ArticlePubMedGoogle Scholar
- Hirsch R, Dent C, Pfriem H, Allen J, Beekman RH, Ma Q, Dastrala S, Bennett M, Mitsnefes M, Devarajan P: NGAL is an early predictive biomarker of contrast-induced nephropathy in children. Pediatr Nephrol 2007, 22: 2089-2095. 10.1007/s00467-007-0601-4View ArticlePubMedGoogle Scholar
- Nickolas TL, O'Rourke MJ, Yang J, Sise ME, Canetta PA, Barasch N, Buchen C, Khan F, Mori K, Giglio J, Devarajan P, Barasch J: Sensitivity and specificity of a single emergency department measurement of urinary neutrophil gelatinase-associated lipocalin for diagnosing acute kidney injury. Ann Intern Med 2008, 148: 810-819.PubMed CentralView ArticlePubMedGoogle Scholar
- de Geus HR, Bakker J, Lesaffre EM, le Noble JL: Neutrophil gelatinase-associated lipocalin at ICU admission predicts for acute kidney injury in adult patients. Am J Respir Crit Care Med 2011, 183: 907-914. 10.1164/rccm.200908-1214OCView ArticlePubMedGoogle Scholar
- Wheeler DS, Devarajan P, Ma Q, Harmon K, Monaco M, Cvijanovich N, Wong HR: Serum neutrophil gelatinase-associated lipocalin (NGAL) as a marker of acute kidney injury in critically ill children with septic shock. Crit Care Med 2008, 36: 1297-1303. 10.1097/CCM.0b013e318169245aPubMed CentralView ArticlePubMedGoogle Scholar
- Siew ED, Ware LB, Gebretsadik T, Shintani A, Moons KG, Wickersham N, Bossert F, Ikizler TA: Urine neutrophil gelatinase-associated lipocalin moderately predicts acute kidney injury in critically ill adults. J Am Soc Nephrol 2009, 20: 1823-1832. 10.1681/ASN.2008070673PubMed CentralView ArticlePubMedGoogle Scholar
- Dickstein K: ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2008: application of natriuretic peptides. Reply. Eur Heart J 2008 2009, 30: 383.Google Scholar
- Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, Warnock DG, Levin A: Acute Kidney Injury Network: report of an initiative to improve outcomes in acute kidney injury. Crit Care 2007, 11: R31. 10.1186/cc5713PubMed CentralView ArticlePubMedGoogle Scholar
- Aghel A, Shrestha K, Mullens W, Borowski A, Tang WH: Serum neutrophil gelatinase-associated lipocalin (NGAL) in predicting worsening renal function in acute decompensated heart failure. J Card Fail 2010, 16: 49-54. 10.1016/j.cardfail.2009.07.003PubMed CentralView ArticlePubMedGoogle Scholar
- Alvelos M, Pimentel R, Pinho E, Gomes A, Lourenco P, Teles MJ, Almeida P, Guimaraes JT, Bettencourt P: Neutrophil gelatinase-associated lipocalin in the diagnosis of type 1 cardio-renal syndrome in the general ward. Clin J Am Soc Nephrol 2011, 6: 476-481. 10.2215/CJN.06140710PubMed CentralView ArticlePubMedGoogle Scholar
- Tang WH, Mullens W: Cardiorenal syndrome in decompensated heart failure. Heart 2010, 96: 255-260. 10.1136/hrt.2009.166256View ArticlePubMedGoogle Scholar
- Ljungman S, Laragh JH, Cody RJ: Role of the kidney in congestive heart failure. Relationship of cardiac index to kidney function. Drugs 1990,39(Suppl 4):10-21. discussion 22-14View ArticlePubMedGoogle Scholar
- Damman K, van Deursen VM, Navis G, Voors AA, van Veldhuisen DJ, Hillege HL: Increased central venous pressure is associated with impaired renal function and mortality in a broad spectrum of patients with cardiovascular disease. J Am Coll Cardiol 2009, 53: 582-588. 10.1016/j.jacc.2008.08.080View ArticlePubMedGoogle Scholar
- Uthoff H, Breidthardt T, Klima T, Aschwanden M, Arenja N, Socrates T, Heinisch C, Noveanu M, Frischknecht B, Baumann U, Jaeger KA, Mueller C: Central venous pressure and impaired renal function in patients with acute heart failure. Eur J Heart Fail 2011, 13: 432-439. 10.1093/eurjhf/hfq195View ArticlePubMedGoogle Scholar
- Endre ZH, Pickering JW, Walker RJ, Devarajan P, Edelstein CL, Bonventre JV, Frampton CM, Bennett MR, Ma Q, Sabbisetti VS, Vaidya VS, Walcher AM, Shaw GM, Henderson SJ, Nejat M, Schollum JB, George PM: Improved performance of urinary biomarkers of acute kidney injury in the critically ill by stratification for injury duration and baseline renal function. Kidney Int 2011, 79: 1119-1130. 10.1038/ki.2010.555View ArticlePubMedGoogle Scholar
- Lameire NH, Vanholder RC, Van Biesen WA: How to use biomarkers efficiently in acute kidney injury. Kidney Int 2011, 79: 1047-1050. 10.1038/ki.2011.21View ArticlePubMedGoogle Scholar
- Damman K, van Veldhuisen DJ, Navis G, Voors AA, Hillege HL: Urinary neutrophil gelatinase associated lipocalin (NGAL), a marker of tubular damage, is increased in patients with chronic heart failure. Eur J Heart Fail 2008, 10: 997-1000. 10.1016/j.ejheart.2008.07.001View ArticlePubMedGoogle Scholar
- Poniatowski B, Malyszko J, Bachorzewska-Gajewska H, Malyszko JS, Dobrzycki S: Serum neutrophil gelatinase-associated lipocalin as a marker of renal function in patients with chronic heart failure and coronary artery disease. Kidney Blood Press Res 2009, 32: 77-80. 10.1159/000208989View ArticlePubMedGoogle Scholar
- Maisel AS, Mueller C, Fitzgerald R, Brikhan R, Hiestand BC, Iqbal N, Clopton P, van Veldhuisen DJ: Prognostic utility of plasma neutrophil gelatinase-associated lipocalin in patients with acute heart failure: the NGAL EvaLuation Along with B-type NaTriuretic Peptide in acutely decompensated heart failure (GALLANT) trial. Eur J Heart Fail 2011, 13: 846-851. 10.1093/eurjhf/hfr087PubMed CentralView ArticlePubMedGoogle Scholar
- Alvelos M, Lourenco P, Dias C, Amorim M, Rema J, Leite AB, Guimaraes JT, Almeida P, Bettencourt P: Prognostic value of neutrophil gelatinase-associated lipocalin in acute heart failure. Int J Cardiol, in press.
- Devarajan P: Review: neutrophil gelatinase-associated lipocalin: a troponin-like biomarker for human acute kidney injury. Nephrology (Carlton) 2010, 15: 419-428. 10.1111/j.1440-1797.2010.01317.xView ArticleGoogle Scholar
- Bolignano D, Coppolino G, Donato V, Lacquaniti A, Bono C, Buemi M: Neutrophil gelatinase-associated lipocalin (NGAL): a new piece of the anemia puzzle? Med Sci Monit 2010, 16: RA131-135.PubMedGoogle Scholar
- Yan QW, Yang Q, Mody N, Graham TE, Hsu CH, Xu Z, Houstis NE, Kahn BB, Rosen ED: The adipokine lipocalin 2 is regulated by obesity and promotes insulin resistance. Diabetes 2007, 56: 2533-2540. 10.2337/db07-0007View ArticlePubMedGoogle Scholar
- Yndestad A, Landrø L, Ueland T, Dahl CP, Flo TH, Vinge LE, Espevik T, Frøland SS, Husberg C, Christensen G, Dickstein K, Kjekshus J, Øie E, Gullestad L, Aukrust P: Increased systemic and myocardial expression of neutrophil gelatinase-associated lipocalin in clinical and experimental heart failure. Eur Heart J 2009, 30: 1229-1236. 10.1093/eurheartj/ehp088View ArticlePubMedGoogle Scholar
- Haase M, Bellomo R, Devarajan P, Schlattmann P, Haase-Fielitz A: Accuracy of neutrophil gelatinase-associated lipocalin (NGAL) in diagnosis and prognosis in acute kidney injury: a systematic review and meta-analysis. Am J Kidney Dis 2009, 54: 1012-1024. 10.1053/j.ajkd.2009.07.020View ArticlePubMedGoogle Scholar
- Coca SG, Peixoto AJ, Garg AX, Krumholz HM, Parikh CR: The prognostic importance of a small acute decrement in kidney function in hospitalized patients: a systematic review and meta-analysis. Am J Kidney Dis 2007, 50: 712-720. 10.1053/j.ajkd.2007.07.018View ArticlePubMedGoogle Scholar
- Gottlieb SS, Abraham W, Butler J, Forman DE, Loh E, Massie BM, O'Connor CM, Rich MW, Stevenson LW, Young J, Krumholz HM: The prognostic importance of different definitions of worsening renal function in congestive heart failure. J Card Fail 2002, 8: 136-141. 10.1054/jcaf.2002.125289View ArticlePubMedGoogle Scholar
- Worster A, Carpenter C: Incorporation bias in studies of diagnostic tests: how to avoid being biased about bias. CJEM 2008, 10: 174-175.PubMedGoogle Scholar
- Whiting P, Rutjes AW, Reitsma JB, Glas AS, Bossuyt PM, Kleijnen J: Sources of variation and bias in studies of diagnostic accuracy: a systematic review. Ann Intern Med 2004, 140: 189-202.View ArticlePubMedGoogle Scholar
- Forman DE, Butler J, Wang Y, Abraham WT, O'Connor CM, Gottlieb SS, Loh E, Massie BM, Rich MW, Stevenson LW, Young JB, Krumholz HM: Incidence, predictors at admission, and impact of worsening renal function among patients hospitalized with heart failure. J Am Coll Cardiol 2004, 43: 61-67. 10.1016/j.jacc.2003.07.031View ArticlePubMedGoogle Scholar
- Cowie MR, Komajda M, Murray-Thomas T, Underwood J, Ticho B: Prevalence and impact of worsening renal function in patients hospitalized with decompensated heart failure: results of the prospective outcomes study in heart failure (POSH). Eur Heart J 2006, 27: 1216-1222.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.