肝脏 ›› 2016, Vol. 21 ›› Issue (2): 85-88.

• 论著 •    下一篇

血清M30抗原水平对HBV相关慢加急性肝衰竭的预后评估价值

陈榕, 曹竹君, 王云, 项晓刚, 安宝燕, 谢青, 王晖, 郭清   

  1. 200025 上海交通大学医学院附属瑞金医院感染科
  • 收稿日期:2015-11-05 出版日期:2016-02-29 发布日期:2020-06-28
  • 通讯作者: 郭清,Email:13901922856@163.com
  • 基金资助:
    国家自然科学基金(81570560); “十二五”重大专项资助项目(2012ZX10005004-002); 上海市科学技术委员会科技支撑项目(13401902903); 上海市卫生和计划生育委员会重点项目(20134004); 国家临床重点专科建设项目(2012ZX09303-001-001); 苏州市医疗器械与新药专项(ZXY2013003)

The prognostic value of serum M30-antigen levels in patients with HBV-related acute-on-chronic liver failure

CHEN Rong, CAO Zhu-jun, WANG Yun, XIANG Xiao-gang, AN Bao-yan, XIE Qing, WANG Hui, GUO Qing   

  1. Department of Infectious Diseases, Ruijin Hospital, Shanghai 200025, China
  • Received:2015-11-05 Online:2016-02-29 Published:2020-06-28
  • Contact: GUO Qing,Email:13901922856@163.com

摘要: 目的 探索HBV感染后不同疾病阶段的肝细胞凋亡水平及其对HBV相关慢加急性肝衰竭(HBV-ACLF)预后的评估价值。方法 前瞻性纳入40例慢性乙型肝炎(CHB)、40例乙型肝炎肝硬化(HBV-LC)以及54例HBV-ACLF患者,同时设立40例健康对照(HC)。针对HBV-ACLF患者随访3个月,根据随访结果分为存活组及死亡组。检测所有研究对象血清角蛋白18凋亡特异性裂解片段M30抗原水平作为反映肝细胞凋亡水平的间接指标。结果 CHB、HBV-LC及HBV-ACLF组血清M30抗原水平分别为145.24(IQR 86.31,206.39)U/L,213.42(IQR 147.30,391.28)U/L及762.67(IQR 492.45,1395.24)U/L,均显著高于HC组[60.34(IQR 50.58,67.64)U/L](P<0.01)。随着疾病严重程度升高,血清M30抗原呈现递增趋势,尤以HBV-ACLF组最高,显著高于CHB(P<0.01)及HBV-LC组(P<0.01)。M30抗原与ALT、AST、TBil、PT、INR以及HBV DNA呈显著正相关(均P<0.01),与Alb呈显著负相关(P<0.01)。HBV-ACLF 随访3个月死亡组患者血清M30抗原水平[1175.18(IQR 756.57,3224.94)U/L]显著高于存活组患者[491.39(IQR 264.23,657.17)U/L](P<0.01)。血清M30抗原能够良好地预测HBV-ACLF患者3个月预后情况,曲线下面积为0.86(95% CI 0.75~0.96,P<0.01)。结论 肝细胞凋亡水平与HBV感染后的疾病严重程度密切相关,血清M30抗原可能成为HBV相关慢加急性肝衰竭早期预后的候选指标。

关键词: 慢加急性肝衰竭, 乙型肝炎病毒, 细胞凋亡, 预后

Abstract: Objective To investigate the apoptotic level of hepatocytes in patients with chronic hepatitis B virus (HBV) infection at different stages, and to evaluate its prognostic value on HBV-related acute-on-chronic liver failure (HBV-ACLF). Methods A prospective study was carried out in 174 patients including 40 chronic hepatitis B (CHB), 40 HBV-related liver cirrhosis (HBV-LC), 54 HBV-ACLF patients and 40 healthy controls (HC). HBV-ACLF group were followed up for 3 months and classified into survival and death group. Apoptotic levels of hepatocytes were measured by detecting keratin-18 associated caspase-cleaved fragment, M30-antigen. Results Serum M30-antigen levels in CHB, HBV-LC and HBV-ACLF were 145.24 [interquartile range (IQR 86.31-206.39) U/L, 213.42 (IQR 147.30-391.28) U/L and 762.67 (IQR 492.45-1395.24) U/L respectively, which were significantly (P<0.01) higher than those in HC group [60.34 (IQR 50.58-67.64)U/L]. Moreover, serum M30-antigen levels were gradually elevated as disease severity increased, reaching to peek in HBV-ACLF group, which was significantly higher (P<0.01) than those in CHB and HBV-LC group. M30-antigen level was significantly positively correlated with alanine aminotransferase (ALT), aspartate transaminase (AST), total bilirubin (TBil), prothrombin time (PT), international normalized ratio (INR) and HBV-DNA (all P<0.01), while reversely correlated with albumin (P<0.01). More importantly, serum levels of M30-antigen in the death group [1175.18 (IQR 756.57-3224.94) U/L] were significantly (P<0.01) higher than those in the survival group [491.39 (IQR 264.23-657.17) U/L]. Receiver operating characteristic (ROC) curve analysis demonstrated that serum M30-antigen could well predict 3-month outcome of HBV-ACLF patients, as the area under the curve (AUROC) was 0.86 (95% CI 0.75-0.96, P<0.01). Conclusion Hepatocyte apoptosis is closely associated with the disease severity of chronic HBV infection and markedly elevated in patients with HBV-ACLF. Hepatocytes apoptosis biomarker, M30-antigen, might be a potential indicator for the early prognosis of HBV-ACLF.

Key words: Acute-on-chronic liver failure, Hepatitis B virus, Apoptosis, Prognosis