Prognostic value of M30/M65 for outcome of hepatitis B virus-related acute-on-chronic liver failure

被引:45
作者
Zheng, Su-Jun [1 ]
Liu, Shuang [1 ]
Liu, Mei [1 ]
McCrae, Malcolm A. [2 ]
Li, Jun-Feng [1 ,3 ]
Han, Yuan-Ping [4 ]
Xu, Chun-Hui [5 ,6 ,7 ]
Ren, Feng [1 ]
Chen, Yu [1 ]
Duan, Zhong-Ping [1 ]
机构
[1] Capital Med Univ, Beijing Youan Hosp, Artificial Liver Ctr, Beijing 100069, Peoples R China
[2] Pirbright Inst, Pirbright GU24 ONF, England
[3] Lanzhou Univ, Hosp 1, Dept Infect Dis, Lanzhou 730000, Gansu, Peoples R China
[4] Sichuan Univ, Coll Life Sci, Ctr Growth Metab & Aging Res, Chengdu 610065, Sichuan Provinc, Peoples R China
[5] Chinese Acad Med Sci, Inst Hematol, Tianjin 300020, Peoples R China
[6] Chinese Acad Med Sci, Hosp Blood Dis, Tianjin 300020, Peoples R China
[7] Peking Union Med Coll, Tianjin 300020, Peoples R China
基金
中国国家自然科学基金;
关键词
Acute-on-chronic liver failure; Chronic hepatitis B virus infection; Liver disease stage; Liver disease severity; Serum M65 level; Serum M30 level; Prognostic value; CELL-DEATH; CASPASE ACTIVATION; SOLUBLE FORMS; APOPTOSIS; NECROSIS; CYTOKERATIN-18; PREDICTION; BIOMARKERS; MARKERS;
D O I
10.3748/wjg.v20.i9.2403
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
AIM: To determine the prognostic value of circulating indicators of cell death in acute-on-chronic liver failure (ACLF) patients with chronic hepatitis B virus (HBV) infection as the single etiology. METHODS: Full length and caspase cleaved cytokeratin 18 (detected as M65 and M30 antigens) represent circulating indicators of necrosis and apoptosis. M65 and M30 were identified by enzyme-linked immunosorbent assay in 169 subjects including healthy controls (n = 33), patients with chronic hepatitis B (CHB, n = 55) and patients with ACLF (n = 81). According to the 3-mo survival period, ACLF patients were defined as having spontaneous recovery (n = 33) and non-spontaneous recovery which included deceased patients and those who required liver transplantation (n = 48). RESULTS: Both biomarker levels significantly increased gradually as liver disease progressed (for M65: P < 0.001 for all; for M30: control vs CHB, P = 0.072; others: P < 0.001 for all). In contrast, the M30/M65 ratio was significantly higher in controls compared with CHB patients (P = 0.010) or ACLF patients (P < 0.001). In addition, the area under receiver operating characteristic curve (AUC) analysis demonstrated that both biomarkers had diagnostic value (AUC >= 0.80) in identifying ACLF from CHB patients. Interestingly, it is worth noting that the M30/M65 ratio was significantly different between spontaneous and non-spontaneous recovery in ACLF patients (P = 0.032). The prognostic value of the M30/M65 ratio was compared with the Model for End-Stage Liver Disease (MELD) and Child-Pugh scores at the 3-mo survival period, the AUC of the M30/M65 ratio was 0.66 with a sensitivity of 52.9% and the highest specificity of 92.6% (MELD:AUC = 0.71; sensitivity, 79.4%; specificity, 63.0%; Child-Pugh: AUC = 0.77; sensitivity, 61.8%; specificity, 88.9%). CONCLUSION: M65 and M30 are strongly associated with liver disease severity. The M30/M65 ratio may be a potential prognostic marker for spontaneous recovery in patients with HBV-related ACLF. (C) 2014 Baishideng Publishing Group Co., Limited. All rights reserved.
引用
收藏
页码:2403 / 2411
页数:9
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