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- Publisher Website: 10.1111/j.1440-1746.1989.tb00801.x
- Scopus: eid_2-s2.0-0024580926
- PMID: 2490936
- WOS: WOS:A1989T784900002
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Article: Synergism of chronic alcoholism and hepatitis B infection in liver disease
Title | Synergism of chronic alcoholism and hepatitis B infection in liver disease |
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Authors | |
Keywords | alcoholic liver disease hepatitis B infection synergism. |
Issue Date | 1989 |
Publisher | Wiley-Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/JGH |
Citation | Journal Of Gastroenterology And Hepatology, 1989, v. 4 n. 1, p. 11-16 How to Cite? |
Abstract | One hundred and fifty-seven patients with alcoholic liver disease were studied. Hepatitis B surface antigen (HBsAg) was positive in 20.4% of the patients. Those who were positive for the HBsAg presented at an earlier age, had a lower albumin level, a higher globulin level, a more prolonged prothrombin time, were more likely to have features of cirrhosis in the liver biopsy, and were probably more likely to suffer from hepatic encephalopathy in the follow-up compared with those negative for HBsAg. The mortality of subjects was low both on admission and during follow-up. It is concluded that chronic alcoholism and hepatitis B virus infection act synergistically in producing more severe liver damage and causing cirrhosis at a younger age compared with chronic alcoholism alone. One possible reason for the low mortality of the patients might have been their relatively good nutritional status. |
Persistent Identifier | http://hdl.handle.net/10722/161804 |
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.179 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chung, HT | en_US |
dc.contributor.author | Lai, CL | en_US |
dc.contributor.author | Wu, PC | en_US |
dc.contributor.author | Lok, ASF | en_US |
dc.date.accessioned | 2012-09-05T05:15:11Z | - |
dc.date.available | 2012-09-05T05:15:11Z | - |
dc.date.issued | 1989 | en_US |
dc.identifier.citation | Journal Of Gastroenterology And Hepatology, 1989, v. 4 n. 1, p. 11-16 | en_US |
dc.identifier.issn | 0815-9319 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/161804 | - |
dc.description.abstract | One hundred and fifty-seven patients with alcoholic liver disease were studied. Hepatitis B surface antigen (HBsAg) was positive in 20.4% of the patients. Those who were positive for the HBsAg presented at an earlier age, had a lower albumin level, a higher globulin level, a more prolonged prothrombin time, were more likely to have features of cirrhosis in the liver biopsy, and were probably more likely to suffer from hepatic encephalopathy in the follow-up compared with those negative for HBsAg. The mortality of subjects was low both on admission and during follow-up. It is concluded that chronic alcoholism and hepatitis B virus infection act synergistically in producing more severe liver damage and causing cirrhosis at a younger age compared with chronic alcoholism alone. One possible reason for the low mortality of the patients might have been their relatively good nutritional status. | en_US |
dc.language | eng | en_US |
dc.publisher | Wiley-Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/JGH | en_US |
dc.relation.ispartof | Journal of Gastroenterology and Hepatology | en_US |
dc.subject | alcoholic liver disease | - |
dc.subject | hepatitis B infection | - |
dc.subject | synergism. | - |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Hepatitis B - Complications - Mortality - Pathology | en_US |
dc.subject.mesh | Hepatitis B Surface Antigens - Analysis | en_US |
dc.subject.mesh | Hong Kong - Epidemiology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Liver - Pathology | en_US |
dc.subject.mesh | Liver Diseases, Alcoholic - Complications - Mortality - Pathology | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.title | Synergism of chronic alcoholism and hepatitis B infection in liver disease | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lai, CL:hrmelcl@hku.hk | en_US |
dc.identifier.authority | Lai, CL=rp00314 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1111/j.1440-1746.1989.tb00801.x | - |
dc.identifier.pmid | 2490936 | - |
dc.identifier.scopus | eid_2-s2.0-0024580926 | en_US |
dc.identifier.volume | 4 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 11 | en_US |
dc.identifier.epage | 16 | en_US |
dc.identifier.isi | WOS:A1989T784900002 | - |
dc.publisher.place | Australia | en_US |
dc.identifier.scopusauthorid | Chung, HT=7404007053 | en_US |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_US |
dc.identifier.scopusauthorid | Wu, PC=7403119323 | en_US |
dc.identifier.scopusauthorid | Lok, ASF=35379868500 | en_US |
dc.identifier.issnl | 0815-9319 | - |