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Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study

BACKGROUND: The rates of hepatitis B virus (HBV) infection in rheumatoid arthritis (RA) patients are controversial when considering the reported outcomes. It was speculated that HBV infection status was altered after RA, and variations inn HBV infection rates became apparent. METHODS: To compare the...

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Autores principales: Jia, Yue, Zhang, Jingjing, Mo, Lingfei, Ju, Bomiao, Hu, Nan, Wang, Yanhua, Wang, Pei, Zheng, Jie, He, Lan, Wang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229421/
https://www.ncbi.nlm.nih.gov/pubmed/35751011
http://dx.doi.org/10.1186/s12879-022-07536-7
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author Jia, Yue
Zhang, Jingjing
Mo, Lingfei
Ju, Bomiao
Hu, Nan
Wang, Yanhua
Wang, Pei
Zheng, Jie
He, Lan
Wang, Jing
author_facet Jia, Yue
Zhang, Jingjing
Mo, Lingfei
Ju, Bomiao
Hu, Nan
Wang, Yanhua
Wang, Pei
Zheng, Jie
He, Lan
Wang, Jing
author_sort Jia, Yue
collection PubMed
description BACKGROUND: The rates of hepatitis B virus (HBV) infection in rheumatoid arthritis (RA) patients are controversial when considering the reported outcomes. It was speculated that HBV infection status was altered after RA, and variations inn HBV infection rates became apparent. METHODS: To compare the positive proportions of hepatitis B e antigen (HBeAg) and HBV DNA, a retrospective case–control study was performed between 27 chronic hepatitis B (CHB) patients with RA and 108 age- and gender-matched CHB patients. In addition, the positivity rates of hepatitis B surface antigen (HBsAg) and hepatitis B core antibody (anti-HBc) were surveyed among the 892 RA patients. RESULTS: Compared to CHB patients, CHB patients with RA exhibited lower rates of HBeAg positivity (11.1% vs. 35.2%, P = 0.003), HBV DNA positivity (37.0% vs. 63.9%, P = 0.007) and ALT elevation (11.1% vs. 35.2%, P = 0.024). In the 892 RA patients, the prevalence of HBsAg (3.0%) was lower than that reported in the Chinese national data (7.2%), whereas the anti-HBc positivity rate of 44.6% was higher than that of 34.1%. CONCLUSION: HBV infection status was altered after suffering from RA. Compared to the matched CHB patients, low positive proportions of HBeAg and HBV DNA were observed for CHB patients with RA.
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spelling pubmed-92294212022-06-25 Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study Jia, Yue Zhang, Jingjing Mo, Lingfei Ju, Bomiao Hu, Nan Wang, Yanhua Wang, Pei Zheng, Jie He, Lan Wang, Jing BMC Infect Dis Research BACKGROUND: The rates of hepatitis B virus (HBV) infection in rheumatoid arthritis (RA) patients are controversial when considering the reported outcomes. It was speculated that HBV infection status was altered after RA, and variations inn HBV infection rates became apparent. METHODS: To compare the positive proportions of hepatitis B e antigen (HBeAg) and HBV DNA, a retrospective case–control study was performed between 27 chronic hepatitis B (CHB) patients with RA and 108 age- and gender-matched CHB patients. In addition, the positivity rates of hepatitis B surface antigen (HBsAg) and hepatitis B core antibody (anti-HBc) were surveyed among the 892 RA patients. RESULTS: Compared to CHB patients, CHB patients with RA exhibited lower rates of HBeAg positivity (11.1% vs. 35.2%, P = 0.003), HBV DNA positivity (37.0% vs. 63.9%, P = 0.007) and ALT elevation (11.1% vs. 35.2%, P = 0.024). In the 892 RA patients, the prevalence of HBsAg (3.0%) was lower than that reported in the Chinese national data (7.2%), whereas the anti-HBc positivity rate of 44.6% was higher than that of 34.1%. CONCLUSION: HBV infection status was altered after suffering from RA. Compared to the matched CHB patients, low positive proportions of HBeAg and HBV DNA were observed for CHB patients with RA. BioMed Central 2022-06-24 /pmc/articles/PMC9229421/ /pubmed/35751011 http://dx.doi.org/10.1186/s12879-022-07536-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jia, Yue
Zhang, Jingjing
Mo, Lingfei
Ju, Bomiao
Hu, Nan
Wang, Yanhua
Wang, Pei
Zheng, Jie
He, Lan
Wang, Jing
Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study
title Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study
title_full Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study
title_fullStr Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study
title_full_unstemmed Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study
title_short Low positivity rates for HBeAg and HBV DNA in rheumatoid arthritis patients: a case–control study
title_sort low positivity rates for hbeag and hbv dna in rheumatoid arthritis patients: a case–control study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229421/
https://www.ncbi.nlm.nih.gov/pubmed/35751011
http://dx.doi.org/10.1186/s12879-022-07536-7
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