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Long-Term Follow-up and Quantitative Hepatitis B Surface Antigen Monitoring in North American Chronic HBV Carriers.

Authors :
O'Neil, Conar R.
Congly, Stephen E.
Rose, M. Sarah
Lee, Samuel S.
Borman, Meredith A.
Charlton, Carmen L.
Osiowy, Carla
Swain, Mark G.
Burak, Kelly W.
Coffin, Carla S.
Source :
Annals of Hepatology: Official Journal of the Mexican Association of Hepatology; Mar/Apr2017, Vol. 17 Issue 2, p232-241, 10p
Publication Year :
2018

Abstract

Introduction. Quantitative hepatitis B surface antigen (qHBsAg) combined with HBV DNA may be useful for predicting chronic hepatitis B (CHB) activity and nucleoside analogue (NA) response. Material and methods. In this retrospective cohort study we evaluated qHBsAg levels according to CHB disease phase and among patients on treatment. Random effect logistic regression analysis was used to analyze qHBsAg change with time in the NA-treated cohort. Results. 545 CHB carriers [56% M, median age 48 y (IQR 38-59), 73% Asian] had qHBsAg testing. In the untreated group (44%), 8% were classified as immune tolerant, 10% immune clearance, 40% inactive, and 43% had HBeAg- CHB and the median HBsAg levels were 4.6 (IQR 3.4-4.9), 4.0 (IQR 3.4-4.5), 2.9 (IQR 1.4-3.8), and 3.2 log IU/mL (IQR 2.6-4.0), respectively; p < 0.001. In the NA-treated group (28% entecavir, 68% tenofovir, 4% lamivudine), no significant change in qHBsAg levels occured with time. However, 19% of patients on long-term NA had sustained qHBsAg < 2 log<subscript>10</subscript> IU/mL. Conclusion. qHBsAg titers were associated with CHB phase and remained stable in those on long-term NA. A significant number of treated patients had low-level qHBsAg, of which some may be eligible for treatment discontinuation without risk of flare. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16652681
Volume :
17
Issue :
2
Database :
Complementary Index
Journal :
Annals of Hepatology: Official Journal of the Mexican Association of Hepatology
Publication Type :
Academic Journal
Accession number :
128269485
Full Text :
https://doi.org/10.5604/01.3001.0010.8640