Comparison of HBV RNA and Hepatitis B Core Related Antigen With Conventional HBV Markers Among Untreated Adults With Chronic Hepatitis B in North America. Issue 5 (9th September 2021)
- Record Type:
- Journal Article
- Title:
- Comparison of HBV RNA and Hepatitis B Core Related Antigen With Conventional HBV Markers Among Untreated Adults With Chronic Hepatitis B in North America. Issue 5 (9th September 2021)
- Main Title:
- Comparison of HBV RNA and Hepatitis B Core Related Antigen With Conventional HBV Markers Among Untreated Adults With Chronic Hepatitis B in North America
- Authors:
- Ghany, Marc G.
King, Wendy C.
Lisker‐Melman, Mauricio
Lok, Anna S.F.
Terrault, Norah
Janssen, Harry L.A.
Khalili, Mandana
Chung, Raymond T.
Lee, William M.
Lau, Daryl T.Y.
Cloherty, Gavin A.
Sterling, Richard K. - Abstract:
- Abstract : Background and Aims: The clinical utility of two biomarkers, hepatitis B virus (HBV) RNA and hepatitis B core‐related antigen (HBcrAg), as compared to conventional markers of HBV replication and disease activity, is unclear. Approach and Results: Untreated participants in the North American Hepatitis B Research Network Adult Cohort Study were categorized by chronic hepatitis B (CHB) phases based on HBsAg and HBeAg status and HBV DNA and alanine aminotransferase (ALT) levels. HBV RNA and HBcrAg were measured (Abbott HBV pgRNA Research Assay and Fujirebio Lumipulse Immunoassay, respectively), and cross‐sectional associations with conventional CHB markers were tested. Among 1, 409 participants across all CHB phases, median HBV DNA was 3.8 log10 IU/mL and ALT was 34 U/L. HBV RNA was quantifiable in 99% of HBeAg + and 58% of HBeAg − participants; HBcrAg was quantifiable in 20% of HBeAg + (above linear range in the other 80%) and 51% of HBeAg − participants. Both markers differed across CHB phases ( P < 0.001), with higher levels in the HBeAg + and HBeAg − immune active phases. HBV RNA and HBcrAg correlated moderately strongly with HBV DNA in both HBeAg + and HBeAg − phases (HBV RNA: e + ρ = 0.84; e − ρ = 0.78; HBcrAg: e + ρ = 0.66; e − ρ = 0.56; P for all, <0.001), but with HBsAg levels among HBeAg + phases only (HBV RNA: e + ρ = 0.71; P < 0.001; e − ρ = 0.18; P = 0.56; HBcrAg: e + ρ = 0.51; P < 0.001; e − ρ = 0.27; P < 0.001). Associations of higher HBV RNA andAbstract : Background and Aims: The clinical utility of two biomarkers, hepatitis B virus (HBV) RNA and hepatitis B core‐related antigen (HBcrAg), as compared to conventional markers of HBV replication and disease activity, is unclear. Approach and Results: Untreated participants in the North American Hepatitis B Research Network Adult Cohort Study were categorized by chronic hepatitis B (CHB) phases based on HBsAg and HBeAg status and HBV DNA and alanine aminotransferase (ALT) levels. HBV RNA and HBcrAg were measured (Abbott HBV pgRNA Research Assay and Fujirebio Lumipulse Immunoassay, respectively), and cross‐sectional associations with conventional CHB markers were tested. Among 1, 409 participants across all CHB phases, median HBV DNA was 3.8 log10 IU/mL and ALT was 34 U/L. HBV RNA was quantifiable in 99% of HBeAg + and 58% of HBeAg − participants; HBcrAg was quantifiable in 20% of HBeAg + (above linear range in the other 80%) and 51% of HBeAg − participants. Both markers differed across CHB phases ( P < 0.001), with higher levels in the HBeAg + and HBeAg − immune active phases. HBV RNA and HBcrAg correlated moderately strongly with HBV DNA in both HBeAg + and HBeAg − phases (HBV RNA: e + ρ = 0.84; e − ρ = 0.78; HBcrAg: e + ρ = 0.66; e − ρ = 0.56; P for all, <0.001), but with HBsAg levels among HBeAg + phases only (HBV RNA: e + ρ = 0.71; P < 0.001; e − ρ = 0.18; P = 0.56; HBcrAg: e + ρ = 0.51; P < 0.001; e − ρ = 0.27; P < 0.001). Associations of higher HBV RNA and HBcrAg levels with higher ALT, APRI, and Fibrosis‐4 levels were consistent in HBeAg −, but not HBeAg +, phases. Conclusions: Despite clear relationships between HBV RNA and HBcrAg levels and CHB phases, these markers have limited additional value in differentiating CHB phases because of their strong association with HBV DNA and, to a lesser extent, with clinical disease indicators. … (more)
- Is Part Of:
- Hepatology. Volume 74:Issue 5(2021)
- Journal:
- Hepatology
- Issue:
- Volume 74:Issue 5(2021)
- Issue Display:
- Volume 74, Issue 5 (2021)
- Year:
- 2021
- Volume:
- 74
- Issue:
- 5
- Issue Sort Value:
- 2021-0074-0005-0000
- Page Start:
- 2395
- Page End:
- 2409
- Publication Date:
- 2021-09-09
- Subjects:
- Heart -- Diseases -- Nursing -- Periodicals
Lungs -- Diseases -- Nursing -- Periodicals
Intensive care nursing -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1527-3350 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/hep.32018 ↗
- Languages:
- English
- ISSNs:
- 0270-9139
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.836000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26996.xml