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Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment
BACKGROUND: Hepatitis B surface antigen (HBsAg) loss/seroconversion is considered to be an ideal endpoint for antiviral therapy and a final therapeutic target for chronic hepatitis (CHB). This study aimed to evaluate the HBsAg kinetics in CHB patients during peginterferon-a (Peg-IFN-a) treatment. MA...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7339975/ https://www.ncbi.nlm.nih.gov/pubmed/32587233 http://dx.doi.org/10.12659/MSM.921487 |
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author | Wang, Kaifa Huang, Guangyu Chen, Yagang Wang, Yuming |
author_facet | Wang, Kaifa Huang, Guangyu Chen, Yagang Wang, Yuming |
author_sort | Wang, Kaifa |
collection | PubMed |
description | BACKGROUND: Hepatitis B surface antigen (HBsAg) loss/seroconversion is considered to be an ideal endpoint for antiviral therapy and a final therapeutic target for chronic hepatitis (CHB). This study aimed to evaluate the HBsAg kinetics in CHB patients during peginterferon-a (Peg-IFN-a) treatment. MATERIAL/METHODS: A retrospective cohort study was performed using a case database, which included 151 patients who received Peg-IFN-a treatment and with HBsAg load of no less than 4 time points from May 1, 2018 to January 31, 2019. The HBsAg kinetic pattern was analyzed by Q-type clustering, and a clinical prognostic empirical model was constructed based on the HBsAg kinetic pattern of uncured patients. RESULTS: Changes of HBsAg in 13 functionally cured patients were attributed to 3 kinetic patterns by cluster analysis, and there was a significant positive correlation between functionally cure time and baseline HBsAg. For uncured 116 patients with treatment duration longer than or equal to 56 days, 5 HBsAg kinetic patterns were obtained by cluster analysis, and the clinical prognosis empirical model was established. Finally, 13 new functionally cured patients preliminarily confirmed the rationality of the proposed empirical model. CONCLUSIONS: According to empirical model, we recommend that the therapeutic regime should be timely adjusted to improve sustained response rate and reduce patients’ medical burden for patients with second (Z type) and fifth (Z+W type) kinds of patterns. While for the rest of patterns’ patients, it is recommended to continue treatment for a longer period of time to achieve the desired therapeutic goal. |
format | Online Article Text |
id | pubmed-7339975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73399752020-07-09 Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment Wang, Kaifa Huang, Guangyu Chen, Yagang Wang, Yuming Med Sci Monit Clinical Research BACKGROUND: Hepatitis B surface antigen (HBsAg) loss/seroconversion is considered to be an ideal endpoint for antiviral therapy and a final therapeutic target for chronic hepatitis (CHB). This study aimed to evaluate the HBsAg kinetics in CHB patients during peginterferon-a (Peg-IFN-a) treatment. MATERIAL/METHODS: A retrospective cohort study was performed using a case database, which included 151 patients who received Peg-IFN-a treatment and with HBsAg load of no less than 4 time points from May 1, 2018 to January 31, 2019. The HBsAg kinetic pattern was analyzed by Q-type clustering, and a clinical prognostic empirical model was constructed based on the HBsAg kinetic pattern of uncured patients. RESULTS: Changes of HBsAg in 13 functionally cured patients were attributed to 3 kinetic patterns by cluster analysis, and there was a significant positive correlation between functionally cure time and baseline HBsAg. For uncured 116 patients with treatment duration longer than or equal to 56 days, 5 HBsAg kinetic patterns were obtained by cluster analysis, and the clinical prognosis empirical model was established. Finally, 13 new functionally cured patients preliminarily confirmed the rationality of the proposed empirical model. CONCLUSIONS: According to empirical model, we recommend that the therapeutic regime should be timely adjusted to improve sustained response rate and reduce patients’ medical burden for patients with second (Z type) and fifth (Z+W type) kinds of patterns. While for the rest of patterns’ patients, it is recommended to continue treatment for a longer period of time to achieve the desired therapeutic goal. International Scientific Literature, Inc. 2020-06-26 /pmc/articles/PMC7339975/ /pubmed/32587233 http://dx.doi.org/10.12659/MSM.921487 Text en © Med Sci Monit, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Clinical Research Wang, Kaifa Huang, Guangyu Chen, Yagang Wang, Yuming Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment |
title | Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment |
title_full | Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment |
title_fullStr | Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment |
title_full_unstemmed | Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment |
title_short | Hepatitis B Surface Antigen (HBsAg) Kinetics in Chronic Hepatitis B Patients during Peginterferon Treatment |
title_sort | hepatitis b surface antigen (hbsag) kinetics in chronic hepatitis b patients during peginterferon treatment |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7339975/ https://www.ncbi.nlm.nih.gov/pubmed/32587233 http://dx.doi.org/10.12659/MSM.921487 |
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