Gungor, GokhanAtaseven, HuseyinDemir, AliSolak, YalcinGaipov, AbduzhapparBiyik, MuratOzturk, Bahadir2020-03-262020-03-2620141478-32231478-3231https://dx.doi.org/10.1111/liv.12232https://hdl.handle.net/20.500.12395/31017Background & AimsHepatorenal syndrome (HRS) is a severe complication of cirrhosis which is characterized by renal dysfunction and associated with poor survival. Neutrophil gelatinase-associated lipocalin (NGAL) is a troponin-like biomarker for human acute kidney injury. We aimed to investigate levels of plasma and urine NGAL in HRS and predictive ability of these markers for all-cause mortality, in HRS, stable cirrhosis and control subjects. MethodsA total of 64 patients with cirrhosis (8 patients with type 1 HRS, 22 with type 2 HRS, and 34 without HRS) and 23 control subjects were included in the study. Blood and urine samples were measured with Human NGAL sandwich ELISA. Patients were followed up prospectively. ResultsPatients with type 1 and type 2 HRS had significantly higher plasma and urine NGAL levels compared with stable cirrhosis and control subjects. Cox regression analysis showed that plasma NGAL and MELD-Na scores were independent predictors of mortality. ROC-curve analysis showed that the plot of the plasma NGAL, urine NGAL, MELD-Na and Child-Turcot-Pugh score could predict all-cause mortality in cirrhotic patients' area under the curve (AUC 0.819, 0.686, 0.807 and 0.795 respectively). ConclusionsNGAL could predict mortality in patients with HRS independent of other commonly used risk factors.en10.1111/liv.12232info:eu-repo/semantics/closedAccessacute kidney injurycirrhosishepatorenal syndromemortalityneutrophil gelatinase-associated lipocalinArticle341495723799980Q1WOS:000327977700009Q1