Background Liver cirrhosis (LC) is a leading global cause of morbidity and mortality, with inflammation playing a key role in disease progression and clinical complications of LC. The Neutrophil/Lymphocyte Ratio (NLR), a readily available marker of systemic inflammation, has been linked to short-term adverse outcomes in LC, but data on long-term follow-up are limited. This study aimed to investigate the relationship between NLR and long-term all-cause mortality in an unselected cohort of LC patients. Methods Data were gathered from the Italian multicenter observational study "PRO-LIVER". Patients with available data to calculate NLR at baseline were included. Baseline clinical determinants of NLR and the association of NRL with all-cause mortality at 2-year follow-up were evaluated. Results From the overall cohort (n = 753), 506 patients with LC (31% female, mean age 64.8 +/- 11.9 years) were included in the analysis. Median value of NLR was 2.42 (Interquartile Range [IQR]: 1.61-3.52). At baseline, patients with NLR >= 2.42 were more likely to have Child-Pugh B or C, hepatocellular carcinoma (HCC), or portal vein thrombosis (PVT). After a median follow-up of 21 months, 129 patients died: 44 (17%) with NLR < 2.42 and 85 (34%) with NLR >= 2.42 (p < 0.001). At multiple-adjusted Cox regression analysis, NLR >= 2.42 was independently associated with all-cause mortality (HR: 1.65; 95% CI: 1.12-2.44; p = 0.012), along with age, Child-Pugh C class, HCC and PVT. Conclusions NLR is associated with long-term all-cause mortality in LC. NLR may serve as a potentially easily available tool to aid risk refinement in LC. Trial registration numberClinicalTrials.gov Identifier: NCT01470547.
Neutrophil–lymphocyte ratio is associated with worse outcomes in patients with cirrhosis: insights from the PRO-LIVER Registry / D'Amico, T., Miglionico, M., Cangemi, R., Romiti, G.F., De Fabrizio, B., Fasano, S., Recchia, F., Stefanini, L., Raparelli, V., Violi, F., Basili, S., Di Cola, S., Sabetta, A., Maiorca, F., Buoninfante, G., Rumbolà, L., Stefanini, L., Vestri, A., Toriello, F., Talerico, G., et al.. - In: INTERNAL AND EMERGENCY MEDICINE. - ISSN 1828-0447. - 20:5(2025), pp. 1371-1380. [10.1007/s11739-025-03955-x]
Neutrophil–lymphocyte ratio is associated with worse outcomes in patients with cirrhosis: insights from the PRO-LIVER Registry
Fasano S.;Stefanini L.;Violi F.;Stefanini L.;Vestri A.;Costanzo F.;Purrello F.;Marcacci M.;Cuoghi C.;Ventura P.;Pietrangelo A.;Nobili L.;Santilli F.;Schiavone C.;Gallo P.;Raimondo G.
2025
Abstract
Background Liver cirrhosis (LC) is a leading global cause of morbidity and mortality, with inflammation playing a key role in disease progression and clinical complications of LC. The Neutrophil/Lymphocyte Ratio (NLR), a readily available marker of systemic inflammation, has been linked to short-term adverse outcomes in LC, but data on long-term follow-up are limited. This study aimed to investigate the relationship between NLR and long-term all-cause mortality in an unselected cohort of LC patients. Methods Data were gathered from the Italian multicenter observational study "PRO-LIVER". Patients with available data to calculate NLR at baseline were included. Baseline clinical determinants of NLR and the association of NRL with all-cause mortality at 2-year follow-up were evaluated. Results From the overall cohort (n = 753), 506 patients with LC (31% female, mean age 64.8 +/- 11.9 years) were included in the analysis. Median value of NLR was 2.42 (Interquartile Range [IQR]: 1.61-3.52). At baseline, patients with NLR >= 2.42 were more likely to have Child-Pugh B or C, hepatocellular carcinoma (HCC), or portal vein thrombosis (PVT). After a median follow-up of 21 months, 129 patients died: 44 (17%) with NLR < 2.42 and 85 (34%) with NLR >= 2.42 (p < 0.001). At multiple-adjusted Cox regression analysis, NLR >= 2.42 was independently associated with all-cause mortality (HR: 1.65; 95% CI: 1.12-2.44; p = 0.012), along with age, Child-Pugh C class, HCC and PVT. Conclusions NLR is associated with long-term all-cause mortality in LC. NLR may serve as a potentially easily available tool to aid risk refinement in LC. Trial registration numberClinicalTrials.gov Identifier: NCT01470547.| File | Dimensione | Formato | |
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