Cargando…

Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment

BACKGROUND: Serum hepatitis B virus RNA (HBV RNA) has been reported to be a surrogate marker of intrahepatic cccDNA during nucleos(t)ide analogs therapy. However, in HBeAg-positive patients treated with peg-interferon (peg-IFN), whether HBV RNA is superior to other HBV markers in reflecting cccDNA p...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xiaomei, Chi, Xiumei, Wu, Ruihong, Xu, Hongqin, Gao, Xiuzhu, Yu, Lei, Liu, Longgen, Zhang, Mingxiang, Tan, Youwen, Niu, Junqi, Jin, Qinglong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789711/
https://www.ncbi.nlm.nih.gov/pubmed/33407619
http://dx.doi.org/10.1186/s12985-020-01471-2
_version_ 1783633300071383040
author Wang, Xiaomei
Chi, Xiumei
Wu, Ruihong
Xu, Hongqin
Gao, Xiuzhu
Yu, Lei
Liu, Longgen
Zhang, Mingxiang
Tan, Youwen
Niu, Junqi
Jin, Qinglong
author_facet Wang, Xiaomei
Chi, Xiumei
Wu, Ruihong
Xu, Hongqin
Gao, Xiuzhu
Yu, Lei
Liu, Longgen
Zhang, Mingxiang
Tan, Youwen
Niu, Junqi
Jin, Qinglong
author_sort Wang, Xiaomei
collection PubMed
description BACKGROUND: Serum hepatitis B virus RNA (HBV RNA) has been reported to be a surrogate marker of intrahepatic cccDNA during nucleos(t)ide analogs therapy. However, in HBeAg-positive patients treated with peg-interferon (peg-IFN), whether HBV RNA is superior to other HBV markers in reflecting cccDNA profile is still unclear. METHODS: Serum HBV RNA, HBcrAg, HBV DNA, and HBsAg were longitudinally assessed among 30 HBeAg-positive patients during 48-week peg-IFN treatment. Besides, intrahepatic cccDNA was detected at baseline and week 48 respectively. Then, the individual correlations between HBV RNA, HBcrAg, HBV DNA, HBsAg, and cccDNA were statistically analyzed. RESULTS: HBV RNA levels decreased more rapidly in patients with HBeAg seroconversion than those without HBeAg seroconversion. Among all patients, cccDNA correlated better with HBV RNA than with HBcrAg, HBV DNA, and HBsAg at baseline. After 48 weeks peg-IFN treatment, cccDNA still correlated more strongly with HBV RNA than other HBV markers. Further analysis indicated that in patients with HBeAg seroconversion cccDNA strongly correlated with HBV RNA and HBcrAg, whereas not correlate with HBV DNA and HBsAg. While in patients without HBeAg seroconversion, cccDNA highly correlated with HBV RNA and HBV DNA, moderately correlated with HBcrAg, and not correlated with HBsAg. CONCLUSION: Compared to HBcrAg, HBV DNA, and HBsAg, serum HBV RNA correlated more strongly with intrahepatic cccDNA levels before and after 48-week peg-IFN treatment. The level of serum HBV RNA may be a superior surrogate marker in reflecting the intrahepatic cccDNA profile in HBeAg-positive patients during peg-IFN treatment. Trial registration ClinicalTrials, NCT03546530. Registered 1 January 2015. https://clinicaltrials.gov/ct2/results?cond=&term=NCT03546530.
format Online
Article
Text
id pubmed-7789711
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-77897112021-01-07 Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment Wang, Xiaomei Chi, Xiumei Wu, Ruihong Xu, Hongqin Gao, Xiuzhu Yu, Lei Liu, Longgen Zhang, Mingxiang Tan, Youwen Niu, Junqi Jin, Qinglong Virol J Research BACKGROUND: Serum hepatitis B virus RNA (HBV RNA) has been reported to be a surrogate marker of intrahepatic cccDNA during nucleos(t)ide analogs therapy. However, in HBeAg-positive patients treated with peg-interferon (peg-IFN), whether HBV RNA is superior to other HBV markers in reflecting cccDNA profile is still unclear. METHODS: Serum HBV RNA, HBcrAg, HBV DNA, and HBsAg were longitudinally assessed among 30 HBeAg-positive patients during 48-week peg-IFN treatment. Besides, intrahepatic cccDNA was detected at baseline and week 48 respectively. Then, the individual correlations between HBV RNA, HBcrAg, HBV DNA, HBsAg, and cccDNA were statistically analyzed. RESULTS: HBV RNA levels decreased more rapidly in patients with HBeAg seroconversion than those without HBeAg seroconversion. Among all patients, cccDNA correlated better with HBV RNA than with HBcrAg, HBV DNA, and HBsAg at baseline. After 48 weeks peg-IFN treatment, cccDNA still correlated more strongly with HBV RNA than other HBV markers. Further analysis indicated that in patients with HBeAg seroconversion cccDNA strongly correlated with HBV RNA and HBcrAg, whereas not correlate with HBV DNA and HBsAg. While in patients without HBeAg seroconversion, cccDNA highly correlated with HBV RNA and HBV DNA, moderately correlated with HBcrAg, and not correlated with HBsAg. CONCLUSION: Compared to HBcrAg, HBV DNA, and HBsAg, serum HBV RNA correlated more strongly with intrahepatic cccDNA levels before and after 48-week peg-IFN treatment. The level of serum HBV RNA may be a superior surrogate marker in reflecting the intrahepatic cccDNA profile in HBeAg-positive patients during peg-IFN treatment. Trial registration ClinicalTrials, NCT03546530. Registered 1 January 2015. https://clinicaltrials.gov/ct2/results?cond=&term=NCT03546530. BioMed Central 2021-01-06 /pmc/articles/PMC7789711/ /pubmed/33407619 http://dx.doi.org/10.1186/s12985-020-01471-2 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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
Wang, Xiaomei
Chi, Xiumei
Wu, Ruihong
Xu, Hongqin
Gao, Xiuzhu
Yu, Lei
Liu, Longgen
Zhang, Mingxiang
Tan, Youwen
Niu, Junqi
Jin, Qinglong
Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment
title Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment
title_full Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment
title_fullStr Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment
title_full_unstemmed Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment
title_short Serum HBV RNA correlated with intrahepatic cccDNA more strongly than other HBV markers during peg-interferon treatment
title_sort serum hbv rna correlated with intrahepatic cccdna more strongly than other hbv markers during peg-interferon treatment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789711/
https://www.ncbi.nlm.nih.gov/pubmed/33407619
http://dx.doi.org/10.1186/s12985-020-01471-2
work_keys_str_mv AT wangxiaomei serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT chixiumei serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT wuruihong serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT xuhongqin serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT gaoxiuzhu serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT yulei serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT liulonggen serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT zhangmingxiang serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT tanyouwen serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT niujunqi serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment
AT jinqinglong serumhbvrnacorrelatedwithintrahepaticcccdnamorestronglythanotherhbvmarkersduringpeginterferontreatment