Peripartum ALT flares predict earlier postpartum HBeAg clearance in highly viremic HBV-infected women: A long-term follow-up study.

JHEP RepJun 25, 2026 (epub)

Wan-Hsin Wen, Chun-Jen Liu, Ming-Wei Lai et al.

✦ AI-curated · Sources linked

In 30 seconds

This multicentre long-term follow-up study examined postpartum HBeAg clearance in 293 HBeAg-positive pregnant women with high HBV viral loads, enrolled in prior trials of tenofovir for prevention of mother-to-child transmission. ALT trajectories from late pregnancy through six months postpartum were classified as flare or stable. Over a median postpartum follow-up of 27.1 months, 50 women cleared HBeAg. A flare-type ALT trajectory independently predicted earlier clearance (HR 10.37; 95% CI 5.44-19.76; p <0.001), with higher cumulative clearance rates than in the stable group at 12, 24, and 60 months.

Key findings

  • Fifty women achieved HBeAg clearance, an incidence of 5.03 per 100 person-years over a median postpartum follow-up of 27.1 months.
  • A flare-type peripartum ALT trajectory predicted earlier HBeAg clearance (HR 10.37; 95% CI 5.44-19.76; p <0.001), adjusted for multiple covariates.
  • Cumulative clearance in flare versus stable groups was 2.3% vs. 0.4% at 12 months, 25.3% vs. 3.9% at 24 months, and 85.9% vs. 11.9% at 60 months.
  • No adverse hepatic outcomes were observed.

Why it matters

The findings link peripartum ALT patterns with the timing of HBeAg clearance in women with high HBV viral loads, extending the focus beyond prevention of mother-to-child transmission. Recognising this association may help clinicians interpret postpartum disease course and consider maternal outcomes when planning follow-up, while the observational follow-up does not establish that ALT flares cause clearance.

What to keep in mind

Postpartum follow-up and antiviral initiation after six months were guided by routine-care reimbursement criteria and shared decision-making, rather than a uniform assigned treatment strategy.

Source

Published in JHEP Rep. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Gastroenterology

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.