# Is there any role for HBV pgRNA in fibrosis and HCC predisposition?

**Authors:** Aikaterini Skeva, Theocharis Konstantinidis, Vasileios Papadopoulos, Maria Panopoulou, Konstantinos Mimidis

PMC · DOI: 10.3389/fmed.2025.1678116 · 2025-11-12

## TL;DR

This study explores whether HBV pgRNA can predict liver fibrosis and HCC risk in patients undergoing treatment for chronic hepatitis B.

## Contribution

The study investigates the potential of HBV pgRNA as a biomarker for fibrosis and HCC, independent of existing scores.

## Key findings

- HBV pgRNA was not independently correlated with FIB-4 after adjusting for multiple factors.
- HBV pgRNA showed no independent correlation with PAGE-B after adjusting for clinical variables.
- HBV pgRNA positivity was associated with cirrhosis but not with treatment duration.

## Abstract

In this cohort, we aimed to study the evolution of pregenomic RNA (pgRNA) during treatment and compare it with other disease scores such as FIB-4 and PAGE-B.

Eighty-eight HBeAg negative CHB who received long-term treatment with NAs were included. A quantitative HBV S antigen (HBsAg) assay was performed, and viral HBV DNA was quantified by Polymerase Chain Reaction (PCR). Finally, viral RNA levels (pre-core RNA (preC RNA) and pgRNA) were analyzed using the RTPCR protocol. The FIB-4 score was calculated for all patients, depicting the cirrhosis course, while the platelet-related PAGE-B score contributed to the 5-year cumulative prognosis of hepatocellular carcinoma (HCC). Statistical multivariate analysis was performed using the R studio and CATREG SPSS optimal scaling algorithm of SPSS 26.0.0.0.

A total of 18.1% of our sample was positive for HBV pgRNA, delineating a positive correlation with cirrhosis and an apparently negative correlation with therapy duration. HBV pgRNA was not independently correlated with FIB-4 (p = 0.137) after adjustment for aminotransferase/alanine transaminase (AST/ALT)1/2, (AST)1/2, 1/platelets (PLT), age, sex, HBsAg, HBV viral load, regimen administered, and therapy duration (ordinal regression ANOVA p < 10−12; Rreg2: 0.794). Moreover, HBV pgRNA was not independently correlated with PAGE-B (p = 0.459) after adjustment for age, sex, AST, 1/PLT, duration of therapy, HBsAg, HBV viral load, regimen administered, and the presence of cirrhosis (ordinal regression ANOVA p < 10−12; Rreg2: 0.800).

Based on our results, further longitudinal studies are needed to assess the potential usefulness of HBV pgRNA as prognosticator of liver fibrosis and susceptibility to HCC.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), chronic hepatitis B (MONDO:0005344), cirrhosis (MONDO:0005155)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** liver fibrosis (MESH:D008103), HCC (MESH:D006528), cirrhosis (MESH:D005355)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12647073/full.md

---
Source: https://tomesphere.com/paper/PMC12647073