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.
Neutrophil-lymphocyte ratio is associated with worse outcomes in patients with cirrhosis: insights from the PRO-LIVER Registry / D'Amico, Tania; Miglionico, Marzia; Cangemi, Roberto; Francesco Romiti, Giulio; De Fabrizio, Benedetta; Fasano, Salvatore; Recchia, Fabrizio; Stefanini, Lucia; Raparelli, Valeria; Violi, Francesco; Basili, Stefania; -LIVER Collaborators, P. R. O.; Palasciano, Giuseppe; D'Alitto, Felicia; Ostilio Palmieri, Vincenzo; Santovito, Daniela; Di Michele, Dario; Croce, Giuseppe; Sacerdoti, David; Brocco, Silvia; Fasolato, Silvano; Cecchetto, Lara; Bombonato, Giancarlo; Bertoni, Michele; Restuccia, Tea; Andreozzi, Paola; Livia Liguori, Maria; Perticone, Francesco; Caroleo, Benedetto; Perticone, Maria; Staltari, Orietta; Manfredini, Roberto; De Giorgi, Alfredo; Averna, Maurizio; Giammanco, Antonina; Granito, Alessandro; Pettinari, Irene; Marinelli, Sara; Bolondi, Luigi; Falsetti, Lorenzo; Salvi, Aldo; Durante-Mangoni, Emanuele; Cesaro, Flavio; Farinaro, Vincenza; Ragone, Enrico; Morana, Ignazio; Andriulli, Angelo; Ippolito, Antonio; Iacobellis, Angelo; Niro, Grazia; Merla, Antonio; Raimondo, Giovanni; Maimone, Sergio; Cacciola, Irene; Varvara, Doriana; Drenaggi, Davide; Staffolani, Silvia; Picardi, Antonio; Vespasiani-Gentilucci, Umberto; Galati, Giovanni; Gallo, Paolo; Davì, Giovanni; Schiavone, Cosima; Santilli, Francesca; Tana, Claudio; Licata, Anna; Soresi, Maurizio; Battista Bianchi, Giovanni; Carderi, Isabella; Pinto, Antonio; Tuttolomondo, Antonino; Ferrari, Giovanni; Gresele, Paolo; Fierro, Tiziana; Morelli, Olivia; Laffi, Giacomo; Giulio Romanelli, Roberto; Arena, Umberto; Stasi, Cristina; Gasbarrini, Antonio; Gargovich, Matteo; Assunta Zocco, Maria; Riccardi, Laura; Elena Ainora, Maria; Capeci, William; Martino, GIUSEPPE PIO; Nobili, Lorenzo; Cavallo, Maurizio; Frugiuele, Pierluigi; Greco, Antonio; Pietrangelo, Antonello; Ventura, Paolo; Cuoghi, Chiara; Marcacci, Matteo; Serviddio, Gaetano; Vendemiale, Gianluigi; Villani, Rosanna; Gargano, Ruggiero; Vidili, Gianpaolo; Di Cesare, Valentina; Masala, Maristella; Delitala, Giuseppe; Invernizzi, Pietro; Di Minno, Giovanni; Tufano, Antonella; Purrello, Francesco; Privitera, Graziella; Forgione, Alessandra; Curigliano, Valentina; Senzolo, Marco; Isabel Rodríguez-Castro, Kryssia; Giannelli, Gianluigi; Serra, Carla; Neri, Sergio; Rizzetto, Mario; Debernardi Venon, Wilma; SVEGLIATI BARONI, Gianluca; Bergamaschi, Gaetano; Masotti, Michela; Costanzo, Filippo; Corazza, GINO ROBERTO; Hugh Caldwell, Stephen; Angelico, Francesco; Del Ben, Maria; Napoleone, Laura; Polimeni, Licia; Proietti, Marco; Raparelli, Valeria; Francesco Romiti, Giulio; Ruscio, Eleonora; Severoni, Andrea; Talerico, Giovanni; Toriello, Filippo; Vestri, Annarita; Stefanini, Lucia; Rumbolà, Lucas; Buoninfante, Giovanni; Maiorca, Francesca; Sabetta, Annamaria; Di Cola, Simone. - In: INTERNAL AND EMERGENCY MEDICINE. - ISSN 1828-0447. - ELETTRONICO. - (2025). [Epub ahead of print] [10.1007/s11739-025-03955-x]
Neutrophil-lymphocyte ratio is associated with worse outcomes in patients with cirrhosis: insights from the PRO-LIVER Registry
Lorenzo FalsettiMembro del Collaboration Group
;Aldo SalviMembro del Collaboration Group
;Silvia StaffolaniMembro del Collaboration Group
;William CapeciMembro del Collaboration Group
;Giuseppe Pio MartinoMembro del Collaboration Group
;Lorenzo NobiliMembro del Collaboration Group
;Gianluca Svegliati BaroniMembro del Collaboration Group
;Gino Roberto CorazzaMembro del Collaboration Group
;
2025-01-01
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.File | Dimensione | Formato | |
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