Prognostic nomogram incorporating neutrophil-to-lymphocyte ratio for early mortality in decompensated liver cirrhosis

被引:54
作者
Lin, Lin
Yang, Fang
Wang, Ya
Su, Shuai
Su, Zhengyan
Jiang, Xihui
Zheng, Yanmin
Deng, You
Lv, Houning
Zhao, Jingwen
Lin, Rui
Wang, Bangmao
Sun, Chao [1 ]
机构
[1] Tianjin Med Univ Gen Hosp, Dept Gastroenterol & Hepatol, Anshan Rd 154, Tianjin 300052, Peoples R China
基金
中国国家自然科学基金;
关键词
Neutrophil-to-lymphocyte ratio; Prognosis; Chronic liver disease; Cytokine; SYSTEMIC INFLAMMATION; IMMUNE DYSFUNCTION; FAILURE; CYTOKINES; DISEASE; MARKER; MODEL;
D O I
10.1016/j.intimp.2018.01.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Neutrophil-to-lymphocyte ratio (NLR) is a marker of systemic inflammation. However, its pre-dictive utility of 30-day mortality remains elusive in decompensated cirrhotics. Aims: We aimed to combine NLR and other variables associated with early mortality of cirrhotics with acute insults in to a predictive nomogram. Methods: We retrospectively analyzed 352 decompensated cirrhotics. The 30-day mortality was regarded as primary outcome. Multivariate Cox analysis was performed, and a NLR-based nomogram was developed. The performance of nomogram was determined in terms of its calibration, discrimination and clinical usefulness. Serum cytokines were evaluated by Milliplex cytokine assay. Results: On multiple analysis, independent factors for early mortality were albumin, MELD and NLR, which were all selected into the nomogram. The nomogram showed good discrimination, with a concordance index of 0.88. Calibration of the nomogram predicted survival corresponding optimally with the actual outcomes. Decision curve analysis indicated our nomogram was useful in clinical practice. Among circulating cytokines we investigated , IL-6 and IL-8 were substantially elevated in cirrhotics compared to healthy subjects. High NLR was positively correlated with the expression of IL-6 and IL-8. Conclusion: The proposed nomogram incorporating NLR offered an individualized predictive tool for 30-day mortality in decompensated cirrhotics. The escalating value of NLR likely implicated excessive inflammatory response.
引用
收藏
页码:58 / 64
页数:7
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