TY - JOUR
T1 - Urinary L-FABP is a promising prognostic biomarker of ACLF and mortality in patients with decompensated cirrhosis
AU - Juanola, Adrià
AU - Graupera, Isabel
AU - Elia, Chiara
AU - Piano, Salvatore
AU - Solé, Cristina
AU - Carol, Marta
AU - Pérez-Guasch, Martina
AU - Bassegoda, Octavi
AU - Escudé, Laia
AU - Rubio, Ana-Belén
AU - Cervera, Marta
AU - Napoleone, Laura
AU - Avitabile, Emma
AU - Ma, Ann T
AU - Fabrellas, Núria
AU - Pose, Elisa
AU - Morales-Ruiz, Manuel
AU - Jiménez, Wladimiro
AU - Torres, Ferran
AU - Crespo, Gonzalo
AU - Solà, Elsa
AU - Ginès, Pere
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Background & Aims: Decompensated cirrhosis (DC) is associated with high mortality, mainly owing to the development of acute-on-chronic liver failure (ACLF). Identifying the patients with DC who are at high risk of mortality and ACLF development is an unmet clinical need. Liver fatty acid-binding protein (L-FABP) is expressed in several organs and correlates with liver and systemic inflammation. Herein, we aimed to assess the prognostic value of L-FABP in patients with DC.Methods: A prospective series of 444 patients hospitalized for DC was divided into 2 cohorts: study cohort (305 patients) and validation cohort (139 patients). L-FABP was measured in urine and plasma samples collected at admission. Neutrophil gelatinase-associated lipocalin (NGAL) was also measured in urine samples for comparison.Results: Urine but not plasma L-FABP correlated with 3-month survival on univariate analysis. On multivariate analysis, urine L-FABP and model for end-stage liver disease (MELD)-Na were the only independent predictors of prognosis. Urine L-FABP levels were higher in patients with ACLF than in those without and also predicted the development of ACLF, together with MELD-Na, during follow-up. In patients with ACLF, urine L-FABP correlated with liver, coagulation, and circulatory failure. Urine L-FABP levels were also increased in patients with acute kidney injury, particularly in those with acute tubular necrosis. The ability of urinary L-FABP to predict survival and ACLF development was confirmed in the validation cohort. Urine NGAL predicted outcome on univariate but not multivariate analysis.Conclusions: Urinary L-FABP levels are independently associated with the 3-month clinical course in patients with DC, in terms of mortality and ACLF development. Urinary L-FABP is a promising prognostic biomarker for patients with DC.Lay summary: Increased levels of liver fatty acid-binding protein (L-FABP), a protein related to lipid metabolism, have been associated with liver-related diseases. The present study analyzed urinary L-FABP levels in 2 independent groups of patients with decompensated cirrhosis and showed that higher urinary L-FABP levels correlated with increased mortality and risk of acute-on- chronic liver failure development. Therefore, urinary L-FABP levels could be useful as a new tool to predict complications in patients with decompensated cirrhosis. (C) 2021 The Authors. Published by Elsevier B.V. on behalf of European Association for the Study of the Liver.
AB - Background & Aims: Decompensated cirrhosis (DC) is associated with high mortality, mainly owing to the development of acute-on-chronic liver failure (ACLF). Identifying the patients with DC who are at high risk of mortality and ACLF development is an unmet clinical need. Liver fatty acid-binding protein (L-FABP) is expressed in several organs and correlates with liver and systemic inflammation. Herein, we aimed to assess the prognostic value of L-FABP in patients with DC.Methods: A prospective series of 444 patients hospitalized for DC was divided into 2 cohorts: study cohort (305 patients) and validation cohort (139 patients). L-FABP was measured in urine and plasma samples collected at admission. Neutrophil gelatinase-associated lipocalin (NGAL) was also measured in urine samples for comparison.Results: Urine but not plasma L-FABP correlated with 3-month survival on univariate analysis. On multivariate analysis, urine L-FABP and model for end-stage liver disease (MELD)-Na were the only independent predictors of prognosis. Urine L-FABP levels were higher in patients with ACLF than in those without and also predicted the development of ACLF, together with MELD-Na, during follow-up. In patients with ACLF, urine L-FABP correlated with liver, coagulation, and circulatory failure. Urine L-FABP levels were also increased in patients with acute kidney injury, particularly in those with acute tubular necrosis. The ability of urinary L-FABP to predict survival and ACLF development was confirmed in the validation cohort. Urine NGAL predicted outcome on univariate but not multivariate analysis.Conclusions: Urinary L-FABP levels are independently associated with the 3-month clinical course in patients with DC, in terms of mortality and ACLF development. Urinary L-FABP is a promising prognostic biomarker for patients with DC.Lay summary: Increased levels of liver fatty acid-binding protein (L-FABP), a protein related to lipid metabolism, have been associated with liver-related diseases. The present study analyzed urinary L-FABP levels in 2 independent groups of patients with decompensated cirrhosis and showed that higher urinary L-FABP levels correlated with increased mortality and risk of acute-on- chronic liver failure development. Therefore, urinary L-FABP levels could be useful as a new tool to predict complications in patients with decompensated cirrhosis. (C) 2021 The Authors. Published by Elsevier B.V. on behalf of European Association for the Study of the Liver.
KW - Acute-On-Chronic Liver Failure
KW - Cirrhosis
KW - Fatty Acid-Binding Proteins
KW - L-FABP
KW - Liver
KW - Mortality
KW - Organ Failure
KW - SURVIVAL
KW - DIAGNOSIS
KW - INJURY
KW - MODEL
KW - SYSTEMIC INFLAMMATION
KW - CHRONIC LIVER-FAILURE
KW - HEPATOCELLULAR DAMAGE
KW - ACID-BINDING PROTEIN
KW - PREDICT MORTALITY
KW - PROGRESSION
KW - Acute-On-Chronic Liver Failure/blood
KW - Multivariate Analysis
KW - Prognosis
KW - Prospective Studies
KW - Biomarkers/analysis
KW - Humans
KW - Middle Aged
KW - Male
KW - Fatty Acid-Binding Proteins/analysis
KW - Statistics, Nonparametric
KW - Female
KW - Kaplan-Meier Estimate
KW - Proportional Hazards Models
KW - Aged
UR - https://portalrecerca.uab.cat/en/publications/f05d54f3-8630-40dc-a23e-16942c1896b7
UR - http://www.scopus.com/inward/record.url?scp=85118881444&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/cca954a2-9a63-3d84-bcab-492e8a04e31b/
U2 - 10.1016/j.jhep.2021.08.031
DO - 10.1016/j.jhep.2021.08.031
M3 - Article
C2 - 34530063
SN - 0168-8278
VL - 76
SP - 107
EP - 114
JO - Journal of hepatology
JF - Journal of hepatology
IS - 1
ER -