中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

Current status of the research on low-level viremia in chronic hepatitis B patients receiving nucleos(t)ide analogues

DOI: 10.3969/j.issn.1001-5256.2021.06.007
  • Received Date: 2021-05-04
  • Accepted Date: 2021-05-12
  • Published Date: 2021-06-20
  • Nucleos(t)ide analogues (NAs), which are widely used as the first-line anti-hepatitis B virus (HBV) drugs in clinical practice, can effectively inhibit the replication of HBV DNA, significantly slow down disease progression in chronic hepatitis B (CHB) patients, and reduce the development of end-stage liver diseases such as liver failure and liver cancer. However, for some CHB patients receiving first-line NAs for 48 weeks or longer, serum HBV DNA is still persistently or intermittently higher than the lower detection of limit of sensitive nucleic acid detection reagents. After discussion by the authors, low-level viremia (LLV) is defined as follows: persistent LLV refers to the condition in which CHB patients, who receive entecavir, tenofovir disoproxil fumarate, or tenofovir alafenamide fumarate for ≥48 weeks, have positive for HBV DNA are positive by two consecutive detections with sensitive quantitative PCR, with an interval of 3-6 months, but < 2000 IU/ml; intermittent LLV refers to serum HBV DNA are positive intermittently by at least three consecutive detections, with an interval of 3-6 months, but HBV DNA < 2000 IU/ml. For the diagnosis of LLV, the issues of poor compliance and drug-resistant mutations should be excluded. LLV might be associated with the increased risk of progression to liver fibrosis, or hepatocellular carcinoma in patients with liver cirrhosis under NA treatment, but there are still controversies over whether the original treatment regimen with NAs should be changed after the onset of LLV. This article summarizes the incidence rate of LLV under NA treatment and the influence of LLV on prognosis and analyzes the possible mechanisms of the osnet of LLV, so as to provide a reference for the management of LLV in patients treated with NAs.

     

  • 志谢参与线上研讨及线下讨论的专家(按姓氏拼音顺序):陈香梅、成军、段钟平、高沿航、韩涛、胡鹏、黄燕、贾继东、江建宁、李军、林炳亮、刘军平、刘燕娜、吕君、王豪、王晖、王磊、魏来、谢青、徐京杭、余祖江、张大志、张缭云、张欣欣、张跃新。此外,本文还经部分中华医学会肝病学分会肝病基础医学与实验诊断协作组成员共同讨论成文。李德瑶、张鹏参与了文献查阅和整理工作。
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