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Article: Evidence of serologic activity in chronic hepatitis B after surface antigen (HBsAg) seroclearance documented by conventional HBsAg assay
Title | Evidence of serologic activity in chronic hepatitis B after surface antigen (HBsAg) seroclearance documented by conventional HBsAg assay |
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Authors | |
Keywords | HBcrAg HBsAg Linearized HBsAg Seroclearance Serology |
Issue Date | 2013 |
Publisher | Springer New York LLC. The Journal's web site is located at http://www.springer.com/west/home/medicine?SGWID=4-10054-70-173733513-0 |
Citation | Hepatology International, 2013, v. 7 n. 1, p. 98-105 How to Cite? |
Abstract | Background: Possible serologic activity after hepatitis B surface antigen (HBsAg) seroclearance documented by conventional assays in chronic hepatitis B (CHB) has not been thoroughly investigated. Methods: We determined the levels of serum hepatitis B virus (HBV) DNA, hepatitis B core-related antigen (HBcrAg), and linearized HBsAg (CLEIA prototype) in 329 CHB patients (72.0% male) after HBsAg seroclearance was documented by a conventional HBsAg assay. Results: The median interval between presentation and HBsAg seroclearance was 69.4 months. The median age at HBsAg seroclearance was 50 years. Assays for serum HBV DNA, HBcrAg, and linearized HBsAg were performed at a median time interval of 11.2 months after HBsAg loss. Linearized HBsAg and HBcrAg were detectable in 85 (25.8%) and 69 (21%) patients, respectively, and one or both serologic markers were detectable in 133 patients (40.4%). Serum HBV DNA was detectable in only 7 patients (2.1%). There was no correlation between linearized HBsAg and HBcrAg levels (r = 0.095, p = 0.924). The incidences of detectable linearized HBsAg and HBcrAg did not differ between patient samples taken at 6-12 and >12 months after HBsAg seroclearance (p = 0.146 and 0.079, respectively). Among patients with detectable serologic markers, median levels of linearized HBsAg (p = 0.581) and HBcrAg (p = 0.951) did not significantly change with time after HBsAg seroclearance. Conclusion: Using novel HBcrAg and linearized HBsAg assays, viral serologic activity after HBsAg seroclearance was demonstrated in more than 40% of CHB patients. These tests have potential applications in diagnosing and prognosticating CHB patients with HBsAg seroclearance. © 2012 Asian Pacific Association for the Study of the Liver. |
Persistent Identifier | http://hdl.handle.net/10722/163465 |
ISSN | 2023 Impact Factor: 5.9 2023 SCImago Journal Rankings: 1.813 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Seto, WK | en_HK |
dc.contributor.author | Tanaka, Y | en_HK |
dc.contributor.author | Wong, DKH | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.contributor.author | Shinkai, N | en_HK |
dc.contributor.author | Yuen, JCH | en_HK |
dc.contributor.author | Tong, T | en_HK |
dc.contributor.author | Fung, J | en_HK |
dc.contributor.author | Hung, IFN | en_HK |
dc.contributor.author | Yuen, MF | en_HK |
dc.date.accessioned | 2012-09-05T05:31:43Z | - |
dc.date.available | 2012-09-05T05:31:43Z | - |
dc.date.issued | 2013 | en_HK |
dc.identifier.citation | Hepatology International, 2013, v. 7 n. 1, p. 98-105 | en_HK |
dc.identifier.issn | 1936-0533 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/163465 | - |
dc.description.abstract | Background: Possible serologic activity after hepatitis B surface antigen (HBsAg) seroclearance documented by conventional assays in chronic hepatitis B (CHB) has not been thoroughly investigated. Methods: We determined the levels of serum hepatitis B virus (HBV) DNA, hepatitis B core-related antigen (HBcrAg), and linearized HBsAg (CLEIA prototype) in 329 CHB patients (72.0% male) after HBsAg seroclearance was documented by a conventional HBsAg assay. Results: The median interval between presentation and HBsAg seroclearance was 69.4 months. The median age at HBsAg seroclearance was 50 years. Assays for serum HBV DNA, HBcrAg, and linearized HBsAg were performed at a median time interval of 11.2 months after HBsAg loss. Linearized HBsAg and HBcrAg were detectable in 85 (25.8%) and 69 (21%) patients, respectively, and one or both serologic markers were detectable in 133 patients (40.4%). Serum HBV DNA was detectable in only 7 patients (2.1%). There was no correlation between linearized HBsAg and HBcrAg levels (r = 0.095, p = 0.924). The incidences of detectable linearized HBsAg and HBcrAg did not differ between patient samples taken at 6-12 and >12 months after HBsAg seroclearance (p = 0.146 and 0.079, respectively). Among patients with detectable serologic markers, median levels of linearized HBsAg (p = 0.581) and HBcrAg (p = 0.951) did not significantly change with time after HBsAg seroclearance. Conclusion: Using novel HBcrAg and linearized HBsAg assays, viral serologic activity after HBsAg seroclearance was demonstrated in more than 40% of CHB patients. These tests have potential applications in diagnosing and prognosticating CHB patients with HBsAg seroclearance. © 2012 Asian Pacific Association for the Study of the Liver. | en_HK |
dc.language | eng | en_US |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://www.springer.com/west/home/medicine?SGWID=4-10054-70-173733513-0 | en_HK |
dc.relation.ispartof | Hepatology International | en_HK |
dc.subject | HBcrAg | en_HK |
dc.subject | HBsAg | en_HK |
dc.subject | Linearized HBsAg | en_HK |
dc.subject | Seroclearance | en_HK |
dc.subject | Serology | en_HK |
dc.title | Evidence of serologic activity in chronic hepatitis B after surface antigen (HBsAg) seroclearance documented by conventional HBsAg assay | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Seto, WK: wkseto2@hku.hk | en_HK |
dc.identifier.email | Wong, DKH: danywong@hku.hk | en_HK |
dc.identifier.email | Lai, CL: hrmelcl@hku.hk | en_HK |
dc.identifier.email | Hung, IFN: ivanhung@hkucc.hku.hk | en_HK |
dc.identifier.email | Yuen, MF: mfyuen@hku.hk | en_HK |
dc.identifier.authority | Seto, WK=rp01659 | en_HK |
dc.identifier.authority | Wong, DKH=rp00492 | en_HK |
dc.identifier.authority | Lai, CL=rp00314 | en_HK |
dc.identifier.authority | Hung, IFN=rp00508 | en_HK |
dc.identifier.authority | Yuen, MF=rp00479 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/s12072-012-9354-7 | en_HK |
dc.identifier.scopus | eid_2-s2.0-84875241425 | en_HK |
dc.identifier.hkuros | 213662 | - |
dc.identifier.spage | 98 | en_HK |
dc.identifier.epage | 105 | en_HK |
dc.identifier.isi | WOS:000316350600012 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Seto, WK=23390675900 | en_HK |
dc.identifier.scopusauthorid | Tanaka, Y=7405315865 | en_HK |
dc.identifier.scopusauthorid | Wong, DKH=7401535819 | en_HK |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_HK |
dc.identifier.scopusauthorid | Shinkai, N=7003826116 | en_HK |
dc.identifier.scopusauthorid | Yuen, JCH=7102620480 | en_HK |
dc.identifier.scopusauthorid | Tong, T=7102587364 | en_HK |
dc.identifier.scopusauthorid | Fung, J=55032286400 | en_HK |
dc.identifier.scopusauthorid | Hung, IFN=7006103457 | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.citeulike | 10463261 | - |
dc.identifier.issnl | 1936-0533 | - |