# Long-term outcomes of baseline grey-zone patients with HBeAg-negative chronic hepatitis B virus infection

**Authors:** Margarita Papatheodoridi, Sofia Paraskevopoulou, Panagiota Ioannidou, Paraskevi Fytili, Dimitrios S. Karagiannakis, Alkistis Papatheodoridi, Stratigoula Sakellariou, Evangelos Cholongitas, Ioannis Vlachogiannakos, George Papatheodoridis

PMC · DOI: 10.1016/j.jhepr.2026.101771 · 2026-02-04

## TL;DR

This study shows that patients with grey-zone HBeAg-negative chronic HBV are at higher risk of liver cancer and other complications compared to typical cases, and need closer monitoring and better treatment strategies.

## Contribution

The study provides real-world data on the long-term outcomes and management of grey-zone HBeAg-negative chronic HBV patients, highlighting their increased risks and treatment needs.

## Key findings

- Grey-zone patients more frequently develop treatment indications and are treated more often than typical HBeAg-negative patients.
- Grey-zone patients have lower HBsAg loss rates and higher risks of hepatocellular carcinoma and liver-related events.
- They represent a large proportion of chronic HBV patients at tertiary centers and require careful monitoring.

## Abstract

The optimal management and outcomes of patients with HBeAg-negative grey-zone (GZe-) chronic HBV infection remain debatable. We assessed the outcomes and real-life management of GZe-patients and compared them to patients with typical HBeAg-negative chronic infection (CIe-).

We included all HBeAg-negative patients with baseline HBV DNA ≤20,000 IU/ml or HBV DNA >20,000 IU/ml and ALT <2x the upper limit of normal (ULN). Among patients without treatment indications in year 1, those with persistently normal ALT (≤ULN) and HBV DNA <2,000 IU/ml were defined as typical CIe-, and all others were classified as GZe-. Outcomes included treatment initiation, HBsAg loss, hepatocellular carcinoma (HCC), and liver-related events (LREs: HCC, decompensated cirrhosis, liver transplantation, or liver-related death).

In total, 1,501 patients with a mean follow-up of 6.0 ± 4.6 years were included (GZe-/CIe-baseline characteristics: 811/690; GZe-/CIe-at year 1: 719/677). Compared with CIe-patients, GZe-patients more frequently developed treatment indications after year 1 (year 5: 13.4% vs. 2.2%; log-rank, p <0.001) and were more frequently treated after year 1 (year 5: 37.6% vs. 4.6%; log-rank, p <0.001). GZe-patients, particularly those with GZe-baseline characteristics, were less likely to achieve HBsAg loss (1-/5-year: 0.1/1.0% vs. 1/3%; log-rank, p = 0.012) and more frequently developed HCC (1-/5-year: 1/3% vs. 0%; log-rank, p <0.001) and LREs (1-/5-year: 1/4% vs. 0.1%; log-rank, p <0.001).

GZe-patients represent a large proportion of patients with chronic HBV seen at tertiary centers and meet treatment indications more frequently than CIe-patients. They also have a lower probability of HBsAg loss and higher risks of HCC and LREs despite treatment initiation in most cases; therefore, their optimal management and timing of treatment initiation require further evaluation.

The outcomes of patients with grey-zone HBeAg-negative chronic HBV infection remain uncertain, hindering their optimal management and timely treatment in clinical practice. Our real-world data from a tertiary HBV center provide valuable insights to guide the management of this patient group. Grey-zone HBeAg-negative patients represent a substantial proportion of the chronic HBV population and require careful monitoring, as they are at increased risk of hepatocellular carcinoma and other liver-related events.

Image 1

•Outcomes of grey-zone HBeAg-negative chronic HBV remain uncertain, hindering optimal management and timely treatment.•Real-world data from an expert HBV center provide insights to guide management of grey-zone HBeAg-negative patients.•Grey-zone HBeAg-negative patients are a large HBV group at higher risk of cancer and liver-related events.

Outcomes of grey-zone HBeAg-negative chronic HBV remain uncertain, hindering optimal management and timely treatment.

Real-world data from an expert HBV center provide insights to guide management of grey-zone HBeAg-negative patients.

Grey-zone HBeAg-negative patients are a large HBV group at higher risk of cancer and liver-related events.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), chronic hepatitis B virus infection (MONDO:0005366)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** Liver fibrosis (MESH:D008103), liver decompensation (MESH:D017093), cancer (MESH:D009369), Cirrhosis (MESH:D005355), chronic (MESH:D002908), chronic hepatitis B virus infection (MESH:D019694), NA (MESH:D000069295), diabetes (MESH:D003920), HCC (MESH:D006528), alcohol abuse (MESH:D000437), chronic infection (MESH:D000088562), infection (MESH:D007239), HBV infection (MESH:D006509)
- **Chemicals:** alcohol (MESH:D000438), GZe (-)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13019599/full.md

---
Source: https://tomesphere.com/paper/PMC13019599