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Time of injury affects urinary biomarker predictive values for acute kidney injury in critically ill, non-septic patients
by
de Geus, Hilde RH
, Groeneveld, AB Johan
, Betjes, Michiel GH
, van Schaik, Ron HN
, Fortrie, Gijs
in
Acute Kidney Injury - mortality
/ Acute Kidney Injury - urine
/ Acute renal failure
/ Acute-Phase Proteins - urine
/ Analysis
/ Biological markers
/ Biomarkers
/ Biomarkers - urine
/ Clinical Research
/ Confidence intervals
/ Consent
/ Critical Illness
/ Enzymes
/ Female
/ Glutathione Transferase - urine
/ Heart surgery
/ Hepatitis A Virus Cellular Receptor 1
/ Hospitals
/ Humans
/ Incidence
/ Intensive care
/ Internal Medicine
/ Kidney diseases
/ Lipocalin-2
/ Lipocalins - urine
/ Male
/ Medicine
/ Medicine & Public Health
/ Membrane Glycoproteins - urine
/ Middle Aged
/ Molecular weight
/ Mortality
/ Nephrology
/ Netherlands - epidemiology
/ Prognosis
/ Proto-Oncogene Proteins - urine
/ Receptors, Virus
/ Reproducibility of Results
/ Research Article
/ Risk Factors
/ Sensitivity and Specificity
/ Sepsis
/ Sepsis - mortality
/ Sepsis - urine
/ Studies
/ Survival Analysis
2013
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Time of injury affects urinary biomarker predictive values for acute kidney injury in critically ill, non-septic patients
by
de Geus, Hilde RH
, Groeneveld, AB Johan
, Betjes, Michiel GH
, van Schaik, Ron HN
, Fortrie, Gijs
in
Acute Kidney Injury - mortality
/ Acute Kidney Injury - urine
/ Acute renal failure
/ Acute-Phase Proteins - urine
/ Analysis
/ Biological markers
/ Biomarkers
/ Biomarkers - urine
/ Clinical Research
/ Confidence intervals
/ Consent
/ Critical Illness
/ Enzymes
/ Female
/ Glutathione Transferase - urine
/ Heart surgery
/ Hepatitis A Virus Cellular Receptor 1
/ Hospitals
/ Humans
/ Incidence
/ Intensive care
/ Internal Medicine
/ Kidney diseases
/ Lipocalin-2
/ Lipocalins - urine
/ Male
/ Medicine
/ Medicine & Public Health
/ Membrane Glycoproteins - urine
/ Middle Aged
/ Molecular weight
/ Mortality
/ Nephrology
/ Netherlands - epidemiology
/ Prognosis
/ Proto-Oncogene Proteins - urine
/ Receptors, Virus
/ Reproducibility of Results
/ Research Article
/ Risk Factors
/ Sensitivity and Specificity
/ Sepsis
/ Sepsis - mortality
/ Sepsis - urine
/ Studies
/ Survival Analysis
2013
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Time of injury affects urinary biomarker predictive values for acute kidney injury in critically ill, non-septic patients
by
de Geus, Hilde RH
, Groeneveld, AB Johan
, Betjes, Michiel GH
, van Schaik, Ron HN
, Fortrie, Gijs
in
Acute Kidney Injury - mortality
/ Acute Kidney Injury - urine
/ Acute renal failure
/ Acute-Phase Proteins - urine
/ Analysis
/ Biological markers
/ Biomarkers
/ Biomarkers - urine
/ Clinical Research
/ Confidence intervals
/ Consent
/ Critical Illness
/ Enzymes
/ Female
/ Glutathione Transferase - urine
/ Heart surgery
/ Hepatitis A Virus Cellular Receptor 1
/ Hospitals
/ Humans
/ Incidence
/ Intensive care
/ Internal Medicine
/ Kidney diseases
/ Lipocalin-2
/ Lipocalins - urine
/ Male
/ Medicine
/ Medicine & Public Health
/ Membrane Glycoproteins - urine
/ Middle Aged
/ Molecular weight
/ Mortality
/ Nephrology
/ Netherlands - epidemiology
/ Prognosis
/ Proto-Oncogene Proteins - urine
/ Receptors, Virus
/ Reproducibility of Results
/ Research Article
/ Risk Factors
/ Sensitivity and Specificity
/ Sepsis
/ Sepsis - mortality
/ Sepsis - urine
/ Studies
/ Survival Analysis
2013
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Time of injury affects urinary biomarker predictive values for acute kidney injury in critically ill, non-septic patients
Journal Article
Time of injury affects urinary biomarker predictive values for acute kidney injury in critically ill, non-septic patients
2013
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Overview
Background
The predictive value of acute kidney injury (AKI) urinary biomarkers may depend on the time interval following tubular injury, thereby explaining in part the heterogeneous performance of these markers that has been reported in the literature. We studied the influence of timing on the predictive values of tubular proteins, measured before the rise of serum creatinine (SCr) in critically ill, non-septic patients.
Methods
Seven hundred adult critically ill patients were prospectively included for urine measurements at four time-points prior to the rise in serum creatinine (T = 0, -16, -20 and -24 h). Patients with sepsis and or AKI at ICU entry were excluded. The urinary excretion of the proteins, neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1 (KIM-1), which are up-regulated in the distal and proximal tubules, respectively, were measured as well as the constitutive cytoplasmatic enzymes, π- and α-glutathione-S-transferase (GST), which are released by the distal and proximal tubules, respectively.
Results
Five hundred and forty-three subjects were eligible for further analyses; however, 49 developed AKI in the first 48 h. Both NGAL (P = 0.001 at T = -24 vs. non-AKI patients) and KIM-1 (P < 0.0001 at T = 0 vs. non-AKI patients) concentrations gradually increased until AKI diagnosis, whereas π- and α-GST peaked at T = -24 before AKI (P = 0.006 and P = 0.002, respectively vs. non-AKI patients) and showed a rapid decline afterwards. The predictive values at T = -24 prior to AKI were modest for π- and α-GST, whereas NGAL sufficiently predicted AKI at T = -24 and its predictive power improved as the time interval to AKI presentation decreased (area under the receiver operating characteristic curve; AUC = 0.79, P < 0.0001). KIM-1 was a good discriminator at T = 0 only (AUC = 0.73, P < 0.0001).
Conclusions
NGAL, KIM-1, pi- and alpha-GST displayed unique and mutually incomparable time dependent characteristics during the development of non-sepsis related AKI. Therefore, the time-relationship between the biomarker measurements and the injurious event influences the individual test results.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V
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