实用肝脏病杂志 ›› 2025, Vol. 28 ›› Issue (5): 659-662.doi: 10.3969/j.issn.1672-5069.2025.05.005

• 病毒性肝炎 • 上一篇    下一篇

ApoB基因多态性对接受聚乙二醇干扰素α治疗的HBeAg阳性慢性乙型肝炎患者疗效的影响*

陈文哲, 王清园, 陈天, 许宇文   

  1. 201203 上海市 上海中医药大学附属曙光医院西药房(陈文哲,许宇文);肝病科(王清园,陈天)
  • 收稿日期:2024-03-01 出版日期:2025-09-10 发布日期:2025-09-19
  • 作者简介:陈文哲,男,38岁,大学本科,主管药师。E-mail:18616017558@163.com
  • 基金资助:
    *上海市卫生健康委员会科研基金青年基金资助项目(编号:20214Y0502)

Impact of apolipoprotein B gene polymorphisms on response to pegylated interferon alpha-2b treatment in patients with serum HBeAg-positive chronic hepatitis B

Chen Wenzhe, Wang Qingyuan, Chen Tian, et al   

  1. Department of Western Pharmacy, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 200000, China
  • Received:2024-03-01 Online:2025-09-10 Published:2025-09-19

摘要: 目的 探讨载脂蛋白B(ApoB)基因多态性对聚乙二醇干扰素-α2b(peg-IFN-α2b)治疗的血清HBeAg阳性的慢性乙型肝炎(CHB)患者应答的影响。方法 2019年5月~2022年5月我院收治的血清HBeAg阳性CHB患者65例,均接受peg-IFN-α治疗48周。采用PCR法检测血清HBV DNA载量,采用电化学发光法检测血清HBsAg和HBeAg水平,采用Asian Screening Array芯片技术检测ApoB基因单核苷酸多态性(SNP)位点。应用多因素Logistic回归分析影响治疗应答的因素。结果 在治疗48 w结束时,本组65例CHB患者获得完全应答(CR)25例(38.5%),部分应答(PR)40例(61.5%);CR组基线血清HBsAg和HBV DNA载量分别为(2.2±0.5)lg IU/mL和(6.1±1.5)lg IU/mL,均显著低于PR组【分别为(6.2±1.7)IU/mL和(7.1±1.3)lg IU/mL,P<0.05】,而血清ALT和AST水平分别为(134.6±17.6)U/L和(112.6±16.3)U/L,均显著高于PR组【分别为(62.6±14.8)U/L和(60.6±10.2)U/L,P<0.05】;在ApoB基因rs10199768基因,CR组AC基因型和A等位基因型占比分别为80.0%和60.0%,均显著高于PR组的37.5%和25.0%(P<0.05);在rs1367117基因,CR组GG基因型和G等位基因频率分别为28.0%和20.0%,均显著低于PR组的67.5%和60.0%,差异均具有统计学意义(P<0.05);多因素Logistic回归分析显示,rs10199768和rs1367117基因多态性是接受peg-IFN-α治疗的HBeAg阳性CHB患者应答的独立影响因素(OR=5.078,OR=4.933,均P<0.05)。结论 影响peg-IFN-α治疗HBeAg阳性CHB患者应答的因素可能很多,开展ApoB基因多态性监测无疑提供了一个崭新的研究方向。

关键词: 乙型肝炎, 聚乙二醇干扰素-α2b, 载脂蛋白B, 基因多态性, 治疗, 应答

Abstract: Objective This study was conducted to explore impact of apolipoprotein B (ApoB) gene polymorphisms on response to pegylated interferon alpha-2b (peg-IFN-α2b) treatment in patients with serum HBeAg-positive chronic hepatitis B (CHB). Methods Sixty-five serum HBeAg-positive patients with CHB were encountered in our hospital between May 2019 and May 2022, and all received peg- IFN-α2b antiviral treatment for 48 weeks. Serum HBsAg and HBeAg, and HBV DNA loads were routinely assayed, and single nucleotide polymorphism (SNP) of ApoB gene was determined by gene chip. Multivariate Logistic regression analysis was applied to predict impacting factors. Results By end of 48-week antiviral treatment, complete response (CR) was 38.5% and partial response (PR) was 61.5%; baseline serum HBsAg and HBV DNA loads in patients with CR were (2.2±0.5)lg IU/mL and (6.1±1.5)lg IU/mL, both significantly lower than [(6.2±1.7)lg IU/mL and (7.1±1.3)lg IU/mL, respectively, P<0.05], while serum ALT and AST levels were (134.6±17.6)U/L and (112.6±16.3)U/L, both significantly higher than [(62.6±14.8)U/L and (60.6±10.2)U/L, respectively, P<0.05] in those with PR; as for ApoB gene rs10199768 locus, percentage of AC genotype and A allele frequencies in patients with CR were 80.0% and 60.0%, both significantly higher than 37.5% and 25.0%(P<0.05) in those with PR; as for rs1367117 gene, percentage of GG genotype and G allele frequencies in patients with CR were 28.0% and 20.0%, both significantly lower than 67.5% and 60.0% in those with PR (P<0.05); multivariate Logistic regression analysis showed that rs10199768 and rs1367117 SNP were independent factors impacting response to peg-IFN-α2b treatment in patients with serum HBeAg positive CHB (OR=5.078, OR=4.933, both P<0.05). Conclusion SNP of ApoB gene might impact response to peg-IFN-α2b antiviral treatment in patients with serum HBeAg positive CHB, and needs further clinical verification.

Key words: Hepatitis B, Pegylated interferon alpha-2b, Apolipoprotein B gene, Polymorphism, Therapy, Response