2020
DOI: 10.5348/100088z04ny2020ra
|View full text |Cite
|
Sign up to set email alerts
|

Quantitative HBsAg titers in relation to disease progression and serum markers of iron metabolism among chronic hepatitis B patients

Abstract: Aims: To investigate quantitative hepatitis B surface antigen (HBsAg) titers in relation to disease progression and serum markers of iron metabolism in chronic hepatitis B (CHB) patients. Methods: A total of 99 treatment-naïve CHB patients [median (min/max) age: 39.0 (17-66) years, 61.6% were males] with HBsAg positivity for at least six months were included in this study. Data on patient demographics, quantitative HBsAg titers (IU/mL), liver enzymes, hepatitis B virus (HBV) DNA levels, fibrosis stage, necroin… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2021
2021
2021
2021

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 28 publications
(47 reference statements)
0
1
0
Order By: Relevance
“…Baseline levels of HBsAg (<3 log 10 IU/mL) and HBV DNA (<3.3 log 10 IU/mL) were associated with a minimal risk of developing HCC after 10–15 years of follow up, with qHBsAg levels as an independent risk factor in HBeAg-negative, treatment-naïve patients, while HBV DNA and ALT levels were better predictors in HBeAg-positive patients [ 125 ]. Although the correlation between qHBsAg and fibrosis stage is still a matter of debate in treatment-naïve patients [ 126 , 127 ], qHBsAg has been found to be a marker of HBV-specific T cell and B cell response. While HBsAg levels were reported to have no impact on the specific immune cell composition, higher HBsAg levels were associated with an exhausted phenotype in CD4+ T cells and with dysfunctional B cells [ 128 ].…”
Section: Novel Hbv Biomarkersmentioning
confidence: 99%
“…Baseline levels of HBsAg (<3 log 10 IU/mL) and HBV DNA (<3.3 log 10 IU/mL) were associated with a minimal risk of developing HCC after 10–15 years of follow up, with qHBsAg levels as an independent risk factor in HBeAg-negative, treatment-naïve patients, while HBV DNA and ALT levels were better predictors in HBeAg-positive patients [ 125 ]. Although the correlation between qHBsAg and fibrosis stage is still a matter of debate in treatment-naïve patients [ 126 , 127 ], qHBsAg has been found to be a marker of HBV-specific T cell and B cell response. While HBsAg levels were reported to have no impact on the specific immune cell composition, higher HBsAg levels were associated with an exhausted phenotype in CD4+ T cells and with dysfunctional B cells [ 128 ].…”
Section: Novel Hbv Biomarkersmentioning
confidence: 99%