Peiyao Fan , Fuchuan Wang , Yi Dong , Jianguo Yan , Lili Cao , Yinjie Gao , Zhiqiang Xu , Yanwei Zhong , Min Zhang
{"title":"Early serum PreS1 levels are predictive of HBsAg loss in interferon-alpha treated children with HBeAg-positive chronic hepatitis B","authors":"Peiyao Fan , Fuchuan Wang , Yi Dong , Jianguo Yan , Lili Cao , Yinjie Gao , Zhiqiang Xu , Yanwei Zhong , Min Zhang","doi":"10.1016/j.cca.2025.120661","DOIUrl":null,"url":null,"abstract":"<div><h3>Background and Aim(s)</h3><div>The PreS1 surface antigen of large surface proteins (LHBs) plays an important role in predicting clinical outcomes in adults with chronic hepatitis B (CHB). This study aimed to determine whether PreS1 levels can predict HBsAg loss in children with HBeAg-positive CHB undergoing a 48-week interferon-alpha (IFN-α) therapy protocol.</div></div><div><h3>Methods</h3><div>We conducted a retrospective analysis of 133 children with CHB. Biomarkers and clinical outcomes were assessed every three months. The area under the receiver operating characteristic (AUROC) curve was calculated to evaluate the predictive value of different biomarkers for HBsAg loss at the 48-week end-point.</div></div><div><h3>Results</h3><div>At the end of the 48-week IFN-α therapy, HBsAg loss was achieved in 16.5 % (22/133) of patients. PreS1 levels were positively correlated with serum quantitative HBsAg (qHBsAg) and hepatitis B virus (HBV) DNA levels. At baseline, only the PreS1/qHBsAg ratio predicted HBsAg loss at week 48 (AUROC = 0.661, <em>p</em> = 0.015). At week 12, PreS1 levels also predicted HBsAg loss at week 48 (AUROC = 0.875, <em>p</em> < 0.001).</div></div><div><h3>Conclusions</h3><div>Early serum PreS1 levels and the PreS1/qHBsAg ratio may serve as useful predictors of HBsAg loss in children with CHB receiving IFN-α therapy, providing potential guidance for clinical decision-making.</div></div>","PeriodicalId":10205,"journal":{"name":"Clinica Chimica Acta","volume":"579 ","pages":"Article 120661"},"PeriodicalIF":2.9000,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinica Chimica Acta","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009898125005406","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background and Aim(s)
The PreS1 surface antigen of large surface proteins (LHBs) plays an important role in predicting clinical outcomes in adults with chronic hepatitis B (CHB). This study aimed to determine whether PreS1 levels can predict HBsAg loss in children with HBeAg-positive CHB undergoing a 48-week interferon-alpha (IFN-α) therapy protocol.
Methods
We conducted a retrospective analysis of 133 children with CHB. Biomarkers and clinical outcomes were assessed every three months. The area under the receiver operating characteristic (AUROC) curve was calculated to evaluate the predictive value of different biomarkers for HBsAg loss at the 48-week end-point.
Results
At the end of the 48-week IFN-α therapy, HBsAg loss was achieved in 16.5 % (22/133) of patients. PreS1 levels were positively correlated with serum quantitative HBsAg (qHBsAg) and hepatitis B virus (HBV) DNA levels. At baseline, only the PreS1/qHBsAg ratio predicted HBsAg loss at week 48 (AUROC = 0.661, p = 0.015). At week 12, PreS1 levels also predicted HBsAg loss at week 48 (AUROC = 0.875, p < 0.001).
Conclusions
Early serum PreS1 levels and the PreS1/qHBsAg ratio may serve as useful predictors of HBsAg loss in children with CHB receiving IFN-α therapy, providing potential guidance for clinical decision-making.
期刊介绍:
The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)
Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells.
The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.