D'Amico Tania, Miglionico Marzia, Cangemi Roberto, Romiti Giulio Francesco, De Fabrizio Benedetta, Fasano Salvatore, Recchia Fabrizio, Stefanini Lucia, Raparelli Valeria, Violi Francesco, Basili Stefania
Department of Translational and Precision Medicine, Sapienza-University of Rome, Viale del Policlinico 155, 00161, Rome, Italy.
Department of Translational Medicine, University of Ferrara, Ferrara, Italy.
Intern Emerg Med. 2025 May 20. doi: 10.1007/s11739-025-03955-x.
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.
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.
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.
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.
ClinicalTrials.gov Identifier: NCT01470547.
肝硬化(LC)是全球发病和死亡的主要原因,炎症在LC的疾病进展和临床并发症中起关键作用。中性粒细胞/淋巴细胞比值(NLR)是一种易于获得的全身炎症标志物,已被证明与LC的短期不良结局有关,但长期随访数据有限。本研究旨在调查在未选择的LC患者队列中NLR与长期全因死亡率之间的关系。
数据来自意大利多中心观察性研究“PRO-LIVER”。纳入了在基线时可获得计算NLR数据的患者。评估了NLR的基线临床决定因素以及NLR与2年随访时全因死亡率的关联。
在整个队列(n = 753)中,506例LC患者(31%为女性,平均年龄64.8±11.9岁)纳入分析。NLR的中位数为2.42(四分位间距[IQR]:1.61 - 3.52)。在基线时,NLR≥2.42的患者更有可能患有Child-Pugh B或C级、肝细胞癌(HCC)或门静脉血栓形成(PVT)。中位随访21个月后,129例患者死亡:NLR<2.42的患者中有44例(17%),NLR≥2.42的患者中有85例(34%)(p<0.001)。在多因素调整的Cox回归分析中,NLR≥2.42与全因死亡率独立相关(HR:1.65;95%CI:1.12 - 2.44;p = 0.012),同时与年龄、Child-Pugh C级、HCC和PVT相关。
NLR与LC的长期全因死亡率相关。NLR可能作为一种潜在的易于获得的工具,有助于细化LC的风险评估。
ClinicalTrials.gov标识符:NCT01470547。