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Correlation between HBV viral load and other paraclinical parameters in patients with chronic hepatitis B Cover

Correlation between HBV viral load and other paraclinical parameters in patients with chronic hepatitis B

Open Access
|Sep 2025

Abstract

Background: Hepatitis B virus (HBV) infections cause approximately 1.2 million deaths annually, mainly due to complications such as hepatocellular carcinoma and cirrhosis. The key marker used to monitor HBV viraemia and guide treatment is the viral load, often unavailable in resource-limited settings. This study aimed to identify surrogate markers predicting hepatitis viral activity, valuable in areas with limited access to molecular diagnostics.

Methods: A retrospective observational study of 178 chronic hepatitis B patients was conducted at Târgu Mureș Clinical County Hospital between April 2022 and April 2025. The dataset included demographic data, hepatitis B viral load, serological viral markers, blood counts, liver function tests and coagulation parameters. Exclusion criteria consisted of duplicate samples, as well as those with detectable viral loads but missing laboratory determinations. Univariable logistic regression was used to assess associations between abnormal serological parameters and the odds of viral DNA detectability.

Results: Altogether, 178 samples tested for hepatitis viral load were included in the final analysis. Detectable viral DNA was found in 64 (35.96%) patients. A viral load positivity was significantly associated with positive HBsAg (OR = 41.7, 95% CI: 5.50-315.70, p<0.0001), elevated AST levels (OR = 2.46, 95% CI:1.23-4.92, p=0.01), and negative HBeAb (OR = 0.3, 95% CI: 0.09-0.94, p=0.04). Other tested associations were not statistically significant.

Conclusion: HBsAg, HBeAb, and AST levels were significantly associated with hepatitis B DNA detectability, highlighting their potential use in settings lacking molecular assays. Further research with larger cohorts may help identify accessible predictors of viral replication and disease progression.

DOI: https://doi.org/10.2478/amma-2025-0036 | Journal eISSN: 2668-7763 | Journal ISSN: 2668-7755
Language: English
Page range: 223 - 226
Submitted on: Jun 13, 2025
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Accepted on: Jul 30, 2025
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Published on: Sep 18, 2025
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2025 Silvia Donica, Cristina Nicoleta Ciurea, Mihaela-Alexandra Budianu, Anca Cighir, Razvan Lucian Coseriu, Alexandrina Maria Bunea, Adrian Man, published by University of Medicine, Pharmacy, Science and Technology of Targu Mures
This work is licensed under the Creative Commons Attribution 4.0 License.