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Neutrophil-to-Lymphocyte Ratio Correlates With Proinflammatory Neutrophils and Predicts Death in Low Model for End-Stage Liver Disease Patients with Cirrhosis

机译:中性粒细胞与淋巴细胞的比例与促炎性中性粒细胞相关并预测低水平肝硬化终末期肝病患者的死亡

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摘要

The Model for End-Stage Liver Disease (MELD) score has reduced accuracy for liver transplantation (LT) wait-list mortality when MELD ≤20. Neutrophil-to-lymphocyte ratio (NLR) is a biomarker associated with systemic inflammation and may predict cirrhotic decompensation and death. We aimed to evaluate the prognostic utility of high NLR (≥4) for liver-related death among low MELD patients listed for LT, controlling for stage of cirrhosis. In a nested case-control study of cirrhotic adults awaiting LT (February 2002 to May 2011), cases were LT candidates with a liver-related death and MELD ≤20 within 90 days of death. Controls were similar LT candidates who were alive for ≥90 days after LT listing. NLR and other covariates were assessed at the date of lowest MELD, within 90 days of death for cases and within 90 days after listing for controls. There were 41 cases and 66 controls; MELD scores were similar. NLR 25th, 50th, 75th percentile cutoffs were 1.9, 3.1, and 6.8. NLR was ≥4 in 25/41 (61%) cases and in 17/66 (26%) controls. In univariate analysis, NLR (continuous ≥1.9, ≥4, ≥6.8), increasing cirrhosis stage, jaundice, encephalopathy, serum sodium, and albumin and nonselective beta-blocker use were significantly (P < 0.01) associated with liver-related death. In multivariate analysis, NLR of ≥1.9, ≥4, ≥6.8 were each associated with liver-related death. Furthermore, we found that NLR correlated with the frequency of circulating low-density granulocytes, previously identified as displaying proinflammatory properties, as well as monocytes. In conclusion, elevated NLR is associated with liver-related death, independent of MELD and cirrhosis stage. High NLR may aid in determining risk for cirrhotic decompensation, need for increased monitoring, and urgency for expedited LT in candidates with low MELD.
机译:终末期肝病模型(MELD)评分降低了当MELD≤20时肝移植(LT)等候名单死亡率的准确性。中性粒细胞与淋巴细胞的比率(NLR)是与全身性炎症相关的生物标志物,可以预测肝硬化失代偿和死亡。我们的目的是评估在接受LT治疗的低MELD患者中,高NLR(≥4)对肝相关死亡的预后效用,以控制肝硬化的阶段。在一项针对等待肝硬化的肝硬化成人的巢式病例对照研究(2002年2月至2011年5月)中,病例为90岁以下肝相关死亡且其MELD≤20的肝相关死亡。对照组是LT上市后存活≥90天的相似LT候选者。在最低MELD日期,病例死亡后90天内和对照列表列出后90天内评估NLR和其他协变量。病例41例,对照组66例。 MELD分数​​相似。 NLR第25、50、75个百分点的截止值为1.9、3.1和6.8。 25/41(61%)病例和17/66(26%)对照者的NLR≥4。在单变量分析中,NLR(连续≥1.9,≥4,≥6.8),肝硬化阶段增加,黄疸,脑病,血清钠和白蛋白以及非选择性β-受体阻滞剂的使用与肝相关死亡显着相关(P <0.01)。在多变量分析中,NLR≥1.9,≥4,≥6.8均与肝脏相关的死亡有关。此外,我们发现NLR与循环低密度粒细胞和单核细胞的频率有关。总之,NLR升高与肝脏相关的死亡相关,独立于MELD和肝硬化阶段。较高的NLR可能有助于确定肝硬化代偿失调的风险,需要加强监测以及在MELD较低的候选人中加快LT的紧迫性。

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