Evidence map›Paper›PMID 42630452›Full record

ArticleAmerican journal of translational research2026

Serum PreS1 antigen combined with vascular endothelial growth factor can identify low-level hepatitis B virus DNA replication in patients with hepatitis B e antigen-negative chronic infection.

Yue Xie, Yuan Su, Yahui Chen, Yu Wang, Runshi Zhang

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Article in American journal of translational research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yue XieDepartment of Laboratory, Xi'an No. 1 Hospital Xi'an 710002, Shaanxi, China.
Yuan SuSchool of Basic Medicine, Yan'an University School of Medicine Yan'an 716000, Shaanxi, China.
Yahui ChenDepartment of Critical Care Medicine, Xi'an Chang'an District Hospital Xi'an 710118, Shaanxi, China.
Yu WangDepartment of Blood Transfusion, Xi'an No. 1 Hospital Xi'an 710002, Shaanxi, China.
Runshi ZhangDepartment of Laboratory, Xi'an No. 1 Hospital Xi'an 710002, Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with hepatitis B e antigen (HBeAg)-negative chronic hepatitis B virus (HBV) infection exhibiting low-level viremia (HBV DNA 20-2000 IU/mL) represent a clinical "gray zone" with uncertain disease activity. Simple serologic markers are needed when high-sensitivity HBV DNA testing is unavailable.

objectiveTo evaluate serum PreS1 antigen combined with vascular endothelial growth factor (VEGF) for identifying low-level HBV DNA replication in HBeAg-negative chronic HBV infection.

methodsThis single-center retrospective study enrolled 178 patients with HBeAg-negative chronic HBV infection (Xi'an No.1 Hospital, January-June 2025). Based on HBV DNA quantification, patients were classified into suppressed (< 20 IU/mL, n = 118) and low-level HBV DNA replication (20-2000 IU/mL, n = 60) groups. Serum PreS1 antigen (by enzyme-linked immunosorbent assay [ELISA]), and VEGF (by quantitative ELISA) were measured. Logistic regression and receiver operating characteristic (ROC) curves were used.

resultsThe low-level HBV DNA replication group had higher PreS1 positivity (53.3% vs. 4.2%, P < 0.001) and higher VEGF levels (191.75 ± 64.15 vs. 123.36 ± 39.74 pg/mL, P < 0.001). PreS1 positivity (adjusted odds ratio [OR] = 37.209) and each one-standard-deviation increase in VEGF (adjusted OR = 4.596) were independent risk factors. Area under the ROC curve (AUC) for PreS1 alone was 0.745 (sensitivity 53.3%, specificity 95.8%); for VEGF alone, 0.812 (sensitivity 61.7%, specificity 91.5% at 172.32 pg/mL cutoff). The combined model achieved AUC 0.900 (sensitivity 80.0%, specificity 93.2% at probability cutoff 0.328).

conclusionsSerum PreS1 antigen combined with VEGF showed excellent diagnostic performance for identifying low-level HBV DNA replication in HBeAg-negative chronic HBV infection, offering a practical adjunct to high-sensitivity HBV DNA testing.

Indexed as

diagnostic performancehepatitis B e antigen-negativeHepatitis B viruslow viremiaPreS1 antigenvascular endothelial growth factor

Identifiers

PMID42630452
PMCPMC13494419

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.