Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/126252
Title: Neutrophil gelatinase-associated lipocalin is a biomarker of acute-on-chronic liver failure and prognosis in cirrhosis
Author: Ariza Cardenal, Javier
Graupera, Isabel
Coll, M.
Solà, E.
Barreto, R.
García, E.
Moreira, R.
Elia, C.
Morales-Ruiz, M.
Llopis, M.
Huelin, P.
Solé, C.
Fabrellas i Padrès, Núria
Weiss, E.
Nevens, F.
Gerbes, A.
Trebicka, J.
Saliba, F.
Fondevila Campo, Constantino
Hernández-Gea, V.
Fernández, J.
Bernardi, M.
Arroyo, V.
Jiménez Povedano, Wladimiro
Deulofeu, C.
Pavesi, M.
Angeli, Paolo
Jalan, R.
Moreau, R.
Sancho-Bru, P.
Ginès i Gibert, Pere
CANONIC Investigators
EASL CLIF Consortium
Keywords: Insuficiència hepàtica
Cirrosi hepàtica
Pronòstic mèdic
Liver failure
Hepatic cirrhosis
Prognosis
Issue Date: 14-Mar-2016
Publisher: Elsevier
Abstract: BACKGROUND & AIMS: Acute-on-chronic liver failure (ACLF) is a syndrome that occurs in cirrhosis characterized by organ failure(s) and high mortality rate. There are no biomarkers of ACLF. The LCN2 gene and its product, neutrophil gelatinase-associated lipocalin (NGAL), are upregulated in experimental models of liver injury and cultured hepatocytes as a result of injury by toxins or proinflammatory cytokines, particularly Interleukin-6. The aim of this study was to investigate whether NGAL could be a biomarker of ACLF and whether LCN2 gene may be upregulated in the liver in ACLF. METHODS: We analyzed urine and plasma NGAL levels in 716 patients hospitalized for complications of cirrhosis, 148 with ACLF. LCN2 expression was assessed in liver biopsies from 29 additional patients with decompensated cirrhosis with and without ACLF. RESULTS: Urine NGAL was markedly increased in ACLF vs. no ACLF patients (108(35-400) vs. 29(12-73)μg/g creatinine; p<0.001) and was an independent predictive factor of ACLF; the independent association persisted after adjustment for kidney function or exclusion of variables present in ACLF definition. Urine NGAL was also an independent predictive factor of 28day transplant-free mortality together with MELD score and leukocyte count (AUROC 0.88(0.83-0.92)). Urine NGAL improved significantly the accuracy of MELD in predicting prognosis. The LCN2 gene was markedly upregulated in the liver of patients with ACLF. Gene expression correlated directly with serum bilirubin and INR (r=0.79; p<0.001 and r=0.67; p<0.001), MELD (r=0.68; p<0.001) and Interleukin-6 (r=0.65; p<0.001). CONCLUSIONS: NGAL is a biomarker of ACLF and prognosis and correlates with liver failure and systemic inflammation. There is remarkable overexpression of LCN2 gene in the liver in ACLF syndrome. LAY SUMMARY: Urine NGAL is a biomarker of acute-on-chronic liver failure (ACLF). NGAL is a protein that may be expressed in several tissues in response to injury. The protein is filtered by the kidneys due to its small size and can be measured in the urine. Ariza, Graupera and colleagues found in a series of 716 patients with cirrhosis that urine NGAL was markedly increased in patients with ACLF and correlated with prognosis. Moreover, gene coding NGAL was markedly overexpressed in the liver tissue in ACLF.
Note: Versió postprint del document publicat a: https://doi.org/10.1016/j.jhep.2016.03.002
It is part of: Journal of Hepatology, 2016, vol. 65, num. 1, p. 57-65
Related resource: https://doi.org/10.1016/j.jhep.2016.03.002
URI: http://hdl.handle.net/2445/126252
ISSN: 0168-8278
Appears in Collections:Articles publicats en revistes (Infermeria de Salut Pública, Salut mental i Maternoinfantil)
Articles publicats en revistes (Medicina)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Biomedicina)
Articles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)

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