Why do I treat HBeAg-positive chronic hepatitis B patients with a nucleoside analogue

Hong Ma1, Jidong Jia

  • 1Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

Insights

Nucleos(t)ide analogues (NAs) effectively suppress chronic hepatitis B virus (HBV) DNA replication, improving liver histology and patient survival. Long-term NA therapy is crucial for managing CHB and preventing disease progression.

Area of Science:

  • Hepatology
  • Virology
  • Pharmacology

Background:

  • Chronic hepatitis B (CHB) poses a significant global health and economic challenge.
  • Persistent hepatitis B virus (HBV) replication independently predicts disease progression.
  • Sustained HBV replication suppression is key to preventing CHB progression and improving survival.

Purpose of the Study:

  • To evaluate the efficacy and safety of nucleos(t)ide analogues (NAs) in managing CHB.
  • To highlight the role of sustained viral suppression in achieving clinical benefits.
  • To discuss treatment strategies for long-term HBV DNA suppression.

Main Methods:

  • Review of pivotal clinical trials and real-world studies on NA treatment for CHB.
  • Analysis of HBV DNA suppression rates, HBeAg seroconversion, and histological outcomes.
  • Evaluation of NA safety profiles and resistance patterns.

Main Results:

  • NAs demonstrate potent HBV DNA suppression with favorable safety profiles.
  • Extended NA treatment increases HBeAg seroconversion rates.
  • Profound HBV DNA suppression leads to histological improvement and reduced disease progression, even in cirrhosis.

Conclusions:

  • NAs are the preferred first-line treatment for CHB due to high efficacy, safety, and proven clinical benefits.
  • Long-term NA therapy can lead to sustained viral suppression and histological improvement.
  • Treatment strategies should prioritize potent, low-resistance regimens for optimal long-term outcomes.

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