Nie Caiyun, Zhang Lei, Chen Xiaobing, Li Ying, Ha Fushuang, Liu Hua, Han Tao
Department of Oncology, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Henan Cancer Hospital, Zhengzhou, Henan, China.
J Clin Transl Hepatol. 2020 Sep 28;8(3):240-245. doi: 10.14218/JCTH.2020.00045. Epub 2020 Jul 21.
Recent accumulating evidence indicates the biological actions of autotaxin (ATX) in liver disease. However, the relationship between ATX and liver failure has not been reported. The present study aimed to examine alterations of serum ATX in acute-on-chronic liver failure (ACLF) and evaluate whether serum ATX could be useful as an early warning biomarker of ACLF. Serum ATX was measured in 50 patients with hepatitis B-related ACLF, 14 patients with alcohol-related ACLF, 11 patients with hepatitis B-related pre-ACLF, 11 patients with alcohol-related Child-Pugh A cirrhosis, 39 patients with hepatitis B-related Child-Pugh A cirrhosis, 26 patients with chronic hepatitis B, and 38 healthy volunteers by enzyme-linked immunosorbent assay. Serum ATX level was significantly higher in the pre-ACLF group than in the Child-Pugh A cirrhosis and chronic hepatitis B groups but lower than in the ACLF group; furthermore, patients with pre-ACLF deteriorated to ACLF had significantly higher serum ATX levels than pre-ACLF patients that did not progress to ACLF. Serum ATX levels were significantly higher among male ACLF patients with preclinical infection, spontaneous bacterial peritonitis or pneumonia, as compared to patients with ACLF but no spontaneous bacterial peritonitis or pneumonia. Serum ATX levels were well correlated with serum biochemical parameters of liver function and model for end-stage liver disease score. Serum ATX ≥ 584.1 ng/mL was a poor prognostic factor for ACLF (hazard ratio of 4.750, 95% confidence interval of 1.106-20.392, =0.036). Serum ATX level may be a useful early warning biomarker for ACLF.
近期越来越多的证据表明自分泌运动因子(ATX)在肝脏疾病中具有生物学作用。然而,ATX与肝衰竭之间的关系尚未见报道。本研究旨在检测慢性肝病急性肝衰竭(ACLF)患者血清ATX的变化,并评估血清ATX是否可作为ACLF的早期预警生物标志物。采用酶联免疫吸附测定法检测了50例乙型肝炎相关ACLF患者、14例酒精相关ACLF患者、11例乙型肝炎相关ACLF前期患者、11例酒精相关Child-Pugh A级肝硬化患者、39例乙型肝炎相关Child-Pugh A级肝硬化患者、26例慢性乙型肝炎患者及38名健康志愿者的血清ATX。ACLF前期组血清ATX水平显著高于Child-Pugh A级肝硬化组和慢性乙型肝炎组,但低于ACLF组;此外,进展为ACLF的ACLF前期患者血清ATX水平显著高于未进展为ACLF的ACLF前期患者。与无自发性细菌性腹膜炎或肺炎的ACLF患者相比,合并临床前期感染、自发性细菌性腹膜炎或肺炎的男性ACLF患者血清ATX水平显著更高。血清ATX水平与肝功能血清生化参数及终末期肝病模型评分密切相关。血清ATX≥584.1 ng/mL是ACLF的不良预后因素(风险比为4.750,95%置信区间为1.106 - 20.392,P = 0.036)。血清ATX水平可能是ACLF有用的早期预警生物标志物。