肝脏 ›› 2022, Vol. 27 ›› Issue (2): 178-181.

• 肝纤维化及肝硬化 • 上一篇    下一篇

S基因突变对慢性乙型肝炎肝硬化患者血清AFP、PTX3表达及预后的影响

秦旭, 侯志云, 张松, 马丽, 朝浩鹏   

  1. 102600 北京市大兴区人民医院感染科(秦旭,侯志云,张松,马丽);中国中医科学院望京医院检验科(朝浩鹏)
  • 收稿日期:2021-04-27 出版日期:2022-02-28 发布日期:2022-04-19
  • 通讯作者: 朝浩鹏,Email:xqw466@163.com
  • 基金资助:
    北京市大兴区人民医院科技项目(4201810213)

Influence of S gene mutation on the expressions of serum AFP, PTX3 and prognosis of patients with hepatitis B virus-related cirrhosis

QIN Xu1, HOU Zhi-yun1, ZHANG Song1, MA Li1, CHAO Hao-peng2   

  1. 1. Department of Infectious Diseases, Daxing District People's Hospital of Beijing, Beijing 102600, China;
    2. Clinical Laboratory,Wangjing Hospital of China Academy of Chinese Medical Sciences,Beijing 100102,China
  • Received:2021-04-27 Online:2022-02-28 Published:2022-04-19
  • Contact: CHAO Hao-peng,Email:xqw466@163.com

摘要: 目的 探讨S基因突变与AFP、PTX3水平及患者预后的相关性。方法 选取2017年7月至2019年6月于北京市大兴区人民医院治疗的76例慢性乙型肝炎肝硬化患者为研究对象(肝硬化组);同期选取慢性乙型肝炎患者87例作为对照(肝炎组);根据S基因是否发生突变将慢性乙型肝炎肝硬化患者分为S基因突变组22例和S基因未突变组54例。采用半套式PCR检测HBV S基因突变情况;采用酶联免疫吸附(ELISA)法检测血清AFP、PTX3水平;采用全自动生化分析仪检测血清总胆红素(TBil)、天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)水平;Pearson法分析S基因突变慢性乙型肝炎肝硬化患者血清AFP、PTX3水平与肝功能指标相关性;多因素logistic回归分析影响慢性乙型肝炎肝硬化患者预后的因素。结果 肝硬化组TBil水平为(42.59±6.81)μmol/L,S基因突变患者比例为(22/54),高于肝炎组的(25.46±7.32)μmol/L和(9/78),AST(156.83±24.57)U/L、ALT水平(125.31±30.25)U/L低于肝炎组的(238.46±40.22)U/L、(193.74±42.81)U/L,差异均有统计学意义(t/χ2=15.395、9.114、15.362、11.626,均P<0.05);S基因突变组血清AFP(5.98±2.01)ng/mL、PTX3(5.24±1.43)μg/L高于S基因未突变组的(4.86±1.34)ng/mL和(3.84±1.05)μg/L,差异均有统计学意义(t=2.839、4.729,均P<0.05);S基因突变慢性乙型肝炎肝硬化患者血清中AFP、PTX3水平与TBil均呈正相关(r=0.502、0.479,均P<0.05),与AST、ALT均呈负相关(P<0.05);S基因突变与慢性乙型肝炎肝硬化患者预后有关(r=0.553,P<0.05),且发生S基因突变的慢性乙型肝炎肝硬化患者中预后不良比例高于预后良好(86.36%比13.64%);S基因突变、AFP是影响慢性乙型肝炎肝硬化患者发生不良预后的独立危险因素(P<0.05)。结论 S基因突变可能导致慢性乙型肝炎肝硬化患者血清AFP、PTX3水平升高,且可能对患者不良预后的预测具有重要意义。

关键词: 慢性乙型肝炎肝硬化, 乙型肝炎病毒S基因突变, 甲胎蛋白, 正五聚蛋白3, 预后

Abstract: Objective To investigate S gene mutation of hepatitis B virus (HBV) and to detect the levels of serum alpha fetoprotein (AFP) and pentraxin 3 (PTX3) in patients with HBV-related cirrhosis. Methods A total of 76 patients with HBV-related cirrhosis admitted to our hospital from July 2017 to June 2019 were selected as the study objects (cirrhosis group). Meanwhile, 87 patients with chronic hepatitis B (CHB) were selected as the control group (hepatitis group). Patients in cirrhosis group were divided into S gene mutation group (22 cases) and S gene nonmutation group (54 cases) according to whether the mutation of S gene occurred. The S gene mutation of HBV was detected by semi-nested polymerase chain reaction (PCR). The levels of AFP and PTX3 were detected by enzyme-linked immunosorbent assay (ELISA). The levels of serum total bilirubin (TBil), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were detected by automatic biochemical analyzer. Pearson method was used to analyze the correlation between liver function indexes and serum levels of AFP, PTX of patients in S gene mutation group. In addition, multivariate logistic regression was used to analyze factors affecting the prognosis of patients with HBV-related cirrhosis. Results The level of TBil [(42.59 ± 6.81) mol/L] and proportion of patients (22/54) with S gene mutation in cirrhosis group were higher than those in hepatitis group [(25.46 ± 7.32), (9/78)], the levels of AST [(156.83 ± 24.57) U/L], ALT [(125.31 ± 30.25) U/L] in cirrhosis group were lower than those in hepatitis group [(238.46 ± 40.22) U/L, (193.74 ± 42.81) U/L] (t=15.395, 9.114, 15.362, 11.626, all P<0.05); The levels of serum AFP (5.98 ± 2.01) ng/mL and PTX3 (5.24 ± 1.43) μg/L in S gene mutation group were higher than those in S gene nonmutation group [(4.86 ± 1.34) ng/mL, (3.84 ± 1.05) μg/L] (t=2.839, 4.729, all P<0.05). The levels of serum AFP and PTX3 were positively correlated with TBil (r=0.502, 0.479, all P<0.05), negatively correlated with AST and ALT (P<0.05) in patients with HBV-related cirrhosis and S gene mutation. S gene mutation was related to the prognosis of patients with HBV-related cirrhosis (r=0.553, P<0.05) and the proportion of poor prognosis was higher than that of good prognosis (86.36% VS 13.64%). S gene mutation and AFP were independent risk factors for the poor prognosis of patients with HBV-related cirrhosis (P<0.05). Conclusion S gene mutation may induce the increased levels of serum AFP and PTX3 in patients with HBV-related cirrhosis, and may be a significant index in predicting the adverse prognosis.

Key words: Hepatitis B virus-related cirrhosis, S gene mutation of hepatitis B virus, Alpha fetoprotein, Pentraxin 3, Prognosis