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Neutrophil gelatinase‐associated lipocalin: An early biomarker for predicting acute kidney injury and severity in patients with acute pancreatitis
by
Siddappa, Pradeep K
, Jha, Vivekanand
, Kochhar, Rakesh
, Sarotra, Pooja
, Gupta, Vikas
, Medhi, Bikas
in
Alcohol
/ Biomarkers
/ Blood & organ donations
/ Failure
/ Intensive care
/ Kidney diseases
/ Mortality
/ Neutrophils
/ Original
/ Pancreatitis
/ Patients
/ Surgery
/ Urine
2019
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Neutrophil gelatinase‐associated lipocalin: An early biomarker for predicting acute kidney injury and severity in patients with acute pancreatitis
by
Siddappa, Pradeep K
, Jha, Vivekanand
, Kochhar, Rakesh
, Sarotra, Pooja
, Gupta, Vikas
, Medhi, Bikas
in
Alcohol
/ Biomarkers
/ Blood & organ donations
/ Failure
/ Intensive care
/ Kidney diseases
/ Mortality
/ Neutrophils
/ Original
/ Pancreatitis
/ Patients
/ Surgery
/ Urine
2019
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Do you wish to request the book?
Neutrophil gelatinase‐associated lipocalin: An early biomarker for predicting acute kidney injury and severity in patients with acute pancreatitis
by
Siddappa, Pradeep K
, Jha, Vivekanand
, Kochhar, Rakesh
, Sarotra, Pooja
, Gupta, Vikas
, Medhi, Bikas
in
Alcohol
/ Biomarkers
/ Blood & organ donations
/ Failure
/ Intensive care
/ Kidney diseases
/ Mortality
/ Neutrophils
/ Original
/ Pancreatitis
/ Patients
/ Surgery
/ Urine
2019
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Neutrophil gelatinase‐associated lipocalin: An early biomarker for predicting acute kidney injury and severity in patients with acute pancreatitis
Journal Article
Neutrophil gelatinase‐associated lipocalin: An early biomarker for predicting acute kidney injury and severity in patients with acute pancreatitis
2019
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Overview
Acute kidney injury (AKI) in severe acute pancreatitis (SAP) has a high mortality rate. Traditionally used serum creatinine is an insensitive biomarker for the early detection of AKI. We aimed to study the role of plasma and urinary neutrophil gelatinase-associated lipocalin (NGAL) in predicting AKI and a severe course in patients with acute pancreatitis (AP).
Consecutive patients of AP who presented within 72 h of symptom onset and age- and gender-matched healthy controls were included. Urinary and serum NGAL levels [enzyme-linked immunosorbent assay (ELISA)] were evaluated within 24 h of and 72 h after admission and once in controls. Urine and serum NGAL levels were correlated with development of AKI, severity, and outcomes of AP.
Fifty patients with AP and 30 controls were enrolled. The mean serum and urine NGAL levels in patients on day 1 were significantly higher than the serum and urine NGAL levels in controls (
< 0.001). After excluding patients with AKI on day 1 (
= 10), both serum and urinary NGAL levels on days 1 and 3 were significantly higher in patients who subsequently developed AKI (
= 11) compared to those who did not (
= 29) (
= 0.02, 0.01 and
< 0.001, 0.03). A urinary NGAL level of 221.03 ng/mL on day 1 predicted AKI with a sensitivity and specificity of 82 and 80%, respectively (AUC = 0.9). Mean serum and urinary NGAL levels on day 1 were significantly elevated in patients with SAP compared to those without SAP (
= 0.04 and <0.001).
NGAL levels in urine and serum can predict severity of AP and development of AKI.
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