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Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection.

Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection. Research Abstract Details 

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  • Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection. Abstract Text:

    danny ka-ho wongDanny Ka-Ho Wong,yasuhito tanakaYasuhito Tanaka,ching-lung laiChing-Lung Lai,masashi mizokamiMasashi Mizokami,james fungJames Fung,man-fung yuenMan-Fung Yuen,danny ka-ho wongDanny Ka-Ho Wong,yasuhito tanakaYasuhito Tanaka,ching-lung laiChing-Lung Lai,masashi mizokamiMasashi Mizokami,james fungJames Fung,man-fung yuenMan-Fung Yuen,danny ka-ho wongDanny Ka-Ho Wong,yasuhito tanakaYasuhito Tanaka,ching-lung laiChing-Lung Lai,masashi mizokamiMasashi Mizokami,james fungJames Fung,man-fung yuenMan-Fung Yuen,

    A sensitive chemiluminescence enzyme immunoassay has been developed for hepatitis B virus (HBV) core-related antigen (HBcrAg) detection. We aimed to investigate the usefulness of HBcrAg measurement for monitoring chronic hepatitis B disease. HBcrAg levels were measured by a chemiluminescence enzyme immunoassay in 54 untreated patients and 39 patients treated with either entecavir or lamivudine. The HBcrAg concentration correlated positively with the levels of serum HBV DNA (r = 0.820), intrahepatic total HBV DNA (r = 0.700), and covalently closed circular DNA (cccDNA) (r = 0.664; for all, P values were <0.001). A higher HBcrAg concentration was associated with a greater proportion of hepatitis B core antigen immunostaining. Although the differences were not statistically significant, patients with higher Knodell necroinflammation and fibrosis scores tended to have higher serum HBcrAg concentration levels. In the treated patients, the logarithmic reduction in HBcrAg at week 48 correlated positively with the logarithmic reduction of serum HBV DNA, intrahepatic total HBV DNA, and cccDNA. Of the 31 patients with undetectable serum HBV DNA (<300 copies/ml) at the end of treatment, 20 (65%) still had detectable HBcrAg. A greater reduction in posttreatment HBcrAg concentration was associated with histological improvement and a decrease in hepatitis B core antigen immunostaining. HBcrAg concentrations of <40,000 kU/ml at baseline and <200 kU/ml at week 24 were associated with a higher chance of having undetectable HBV DNA at week 48. In conclusion, serum HBcrAg levels correlated with HBV virological markers and reflected the chronic hepatitis B disease activity in the liver.

    Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection. Publishing Authors By Initials

    dk wongDK Wong,y tanakaY Tanaka,cl laiCL Lai,m mizokamiM Mizokami,j fungJ Fung,mf yuenMF Yuen,dk wongDK Wong,y tanakaY Tanaka,cl laiCL Lai,m mizokamiM Mizokami,j fungJ Fung,mf yuenMF Yuen,dk wongDK Wong,y tanakaY Tanaka,cl laiCL Lai,m mizokamiM Mizokami,j fungJ Fung,mf yuenMF Yuen,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of clinical microbiology

    VOLUME: 45

    Page Numbers: 3942-7

    Journal Abbreviation: J. Clin. Microbiol.

    ISSN: 0095-1137

    DAY: 17

    MONTH: 10

    YEAR: 2007

    Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7505564

    Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection. Keywords Mesh Terms:

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    Grant and Affiliation Information for Hepatitis B virus core-related antigens as markers for monitoring chronic hepatitis B infection.

    AFFILIATION: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Pokfulam Road, Hong Kong SAR, China.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Clin Microbiol

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