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Article: Clinical outcome and virologic profiles of severe hepatitis B exacerbation due to YMDD mutations
Title | Clinical outcome and virologic profiles of severe hepatitis B exacerbation due to YMDD mutations |
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Authors | |
Keywords | Hepatitic decompensation Mortality Severe hepatitis B exacerbation YMDD mutation |
Issue Date | 2003 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jhep |
Citation | Journal Of Hepatology, 2003, v. 39 n. 5, p. 850-855 How to Cite? |
Abstract | Background/Aims: To study the outcome and the virologic profiles of severe hepatitis exacerbations due to YMDD mutants in lamivudine-treated patients. Methods: Eighteen lamivudine-treated patients with severe hepatitis exacerbations due to YMDD mutants were recruited. Laboratory and clinical parameters were monitored. Viral genotypes and YMDD mutations were determined. Results: None of the 18 patients had YMDD wild-type during exacerbations. Three (17%) and 15 (83%) patients had genotypes B and C, respectively. Elevated bilirubin levels and prolonged prothrombin time were found in 11 (61%) and six patients (33%) respectively. Three patients (17%) had adverse outcome with the development of ascites and/or encephalopathy. One of these patients required liver transplantation and one died. Both patients had evidence of cirrhosis before treatment and hepatitis B e antigen (HBeAg) seroreversion from anti-HBe positivity. The remaining 16 patients (89%) have no evidence of pre-existing cirrhosis. Thirty seven percent of patients had normal alanine aminotransferase levels at the last follow-up. The median HBV DNA level at the last follow-up was significantly lower than the pre-treatment level (P = 0.009). Conclusions: Though the majority of patients with severe hepatitis exacerbations due to YMDD mutants had uneventful course, early liver transplantation should be considered in patients with pre-existing cirrhosis and HBeAg seroreversion. © 2003 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/77168 |
ISSN | 2023 Impact Factor: 26.8 2023 SCImago Journal Rankings: 9.857 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yuen, MF | en_HK |
dc.contributor.author | Kato, T | en_HK |
dc.contributor.author | Mizokami, M | en_HK |
dc.contributor.author | Chan, AOO | en_HK |
dc.contributor.author | Yuen, JCH | en_HK |
dc.contributor.author | Yuan, HJ | en_HK |
dc.contributor.author | Wong, DKH | en_HK |
dc.contributor.author | Sum, SM | en_HK |
dc.contributor.author | Ng, IOL | en_HK |
dc.contributor.author | Fan, ST | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.date.accessioned | 2010-09-06T07:29:01Z | - |
dc.date.available | 2010-09-06T07:29:01Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | Journal Of Hepatology, 2003, v. 39 n. 5, p. 850-855 | en_HK |
dc.identifier.issn | 0168-8278 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77168 | - |
dc.description.abstract | Background/Aims: To study the outcome and the virologic profiles of severe hepatitis exacerbations due to YMDD mutants in lamivudine-treated patients. Methods: Eighteen lamivudine-treated patients with severe hepatitis exacerbations due to YMDD mutants were recruited. Laboratory and clinical parameters were monitored. Viral genotypes and YMDD mutations were determined. Results: None of the 18 patients had YMDD wild-type during exacerbations. Three (17%) and 15 (83%) patients had genotypes B and C, respectively. Elevated bilirubin levels and prolonged prothrombin time were found in 11 (61%) and six patients (33%) respectively. Three patients (17%) had adverse outcome with the development of ascites and/or encephalopathy. One of these patients required liver transplantation and one died. Both patients had evidence of cirrhosis before treatment and hepatitis B e antigen (HBeAg) seroreversion from anti-HBe positivity. The remaining 16 patients (89%) have no evidence of pre-existing cirrhosis. Thirty seven percent of patients had normal alanine aminotransferase levels at the last follow-up. The median HBV DNA level at the last follow-up was significantly lower than the pre-treatment level (P = 0.009). Conclusions: Though the majority of patients with severe hepatitis exacerbations due to YMDD mutants had uneventful course, early liver transplantation should be considered in patients with pre-existing cirrhosis and HBeAg seroreversion. © 2003 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jhep | en_HK |
dc.relation.ispartof | Journal of Hepatology | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Hepatitic decompensation | en_HK |
dc.subject | Mortality | en_HK |
dc.subject | Severe hepatitis B exacerbation | en_HK |
dc.subject | YMDD mutation | en_HK |
dc.subject.mesh | Hepatitis B - drug therapy - genetics - physiopathology - virology | - |
dc.subject.mesh | Hepatitis B virus - genetics | - |
dc.subject.mesh | Lamivudine - therapeutic use | - |
dc.subject.mesh | Mutation | - |
dc.subject.mesh | Reverse Transcriptase Inhibitors - therapeutic use | - |
dc.title | Clinical outcome and virologic profiles of severe hepatitis B exacerbation due to YMDD mutations | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0168-8278&volume=39&issue=5&spage=850&epage=855&date=2003&atitle=Clinical+outcome+and+virologic+profiles+of+severe+hepatitis+B+exacerbation+due+to+YMDD+mutations | en_HK |
dc.identifier.email | Yuen, MF: mfyuen@hkucc.hku.hk | en_HK |
dc.identifier.email | Wong, DKH: danywong@hku.hk | en_HK |
dc.identifier.email | Ng, IOL: iolng@hkucc.hku.hk | en_HK |
dc.identifier.email | Fan, ST: stfan@hku.hk | en_HK |
dc.identifier.email | Lai, CL: hrmelcl@hku.hk | en_HK |
dc.identifier.authority | Yuen, MF=rp00479 | en_HK |
dc.identifier.authority | Wong, DKH=rp00492 | en_HK |
dc.identifier.authority | Ng, IOL=rp00335 | en_HK |
dc.identifier.authority | Fan, ST=rp00355 | en_HK |
dc.identifier.authority | Lai, CL=rp00314 | en_HK |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1016/S0168-8278(03)00388-X | en_HK |
dc.identifier.pmid | 14568270 | - |
dc.identifier.scopus | eid_2-s2.0-10744226572 | en_HK |
dc.identifier.hkuros | 86101 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-10744226572&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 39 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 850 | en_HK |
dc.identifier.epage | 855 | en_HK |
dc.identifier.isi | WOS:000186441500025 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Yuen, MF=7102031955 | en_HK |
dc.identifier.scopusauthorid | Kato, T=7405277868 | en_HK |
dc.identifier.scopusauthorid | Mizokami, M=7103318255 | en_HK |
dc.identifier.scopusauthorid | Chan, AOO=7403167965 | en_HK |
dc.identifier.scopusauthorid | Yuen, JCH=7102620480 | en_HK |
dc.identifier.scopusauthorid | Yuan, HJ=7402446707 | en_HK |
dc.identifier.scopusauthorid | Wong, DKH=7401535819 | en_HK |
dc.identifier.scopusauthorid | Sum, SM=6603889132 | en_HK |
dc.identifier.scopusauthorid | Ng, IOL=7102753722 | en_HK |
dc.identifier.scopusauthorid | Fan, ST=7402678224 | en_HK |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_HK |
dc.identifier.issnl | 0168-8278 | - |