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- Publisher Website: 10.1002/hep.1840020605
- Scopus: eid_2-s2.0-0020373510
- PMID: 7141388
- WOS: WOS:A1982PS02600004
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Article: Prednisolone in HBsAg-positive chronic active hepatitis: Histologic evaluation in a controlled prospective study
Title | Prednisolone in HBsAg-positive chronic active hepatitis: Histologic evaluation in a controlled prospective study |
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Authors | |
Issue Date | 1982 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ |
Citation | Hepatology, 1982, v. 2 n. 6, p. 777-783 How to Cite? |
Abstract | To study the value of corticosterone in HBsAg-positive chronic active hepatitis, 18 pairs of liver histology comprising 36 liver biopsies from a prospective, randomized, controlled trial were evaluated. The median interval between the initial and follow-up histology was 8 1/2 months in 8 patients given prednisolone and 8 1/4 months in 10 patients given placebo tablets. Following medication, there was significantly greater erosion of the limiting plate in the prenisolone group (p = 0.039) accompanied by a larger quantity HBsAg (p = 0.045) and HBcAg (p = 0.006) in the liver. We conclude that prednisolone causes immunosuppression permitting enhanced viral multiplication and leads to increased erosion of the limiting plate. Our result also indicates that progression to cirrhosis is unhalted by prednisolone therapy. The histologic findings support clinico-biochemical conclusion that the use of prednisolone is deleterious to patients with HBsAg-positive chronic active hepatitis. |
Persistent Identifier | http://hdl.handle.net/10722/161668 |
ISSN | 2023 Impact Factor: 12.9 2023 SCImago Journal Rankings: 5.011 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wu, PC | en_US |
dc.contributor.author | Lai, CL | en_US |
dc.contributor.author | Lam, KC | en_US |
dc.contributor.author | Ho, J | en_US |
dc.date.accessioned | 2012-09-05T05:13:42Z | - |
dc.date.available | 2012-09-05T05:13:42Z | - |
dc.date.issued | 1982 | en_US |
dc.identifier.citation | Hepatology, 1982, v. 2 n. 6, p. 777-783 | en_US |
dc.identifier.issn | 0270-9139 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/161668 | - |
dc.description.abstract | To study the value of corticosterone in HBsAg-positive chronic active hepatitis, 18 pairs of liver histology comprising 36 liver biopsies from a prospective, randomized, controlled trial were evaluated. The median interval between the initial and follow-up histology was 8 1/2 months in 8 patients given prednisolone and 8 1/4 months in 10 patients given placebo tablets. Following medication, there was significantly greater erosion of the limiting plate in the prenisolone group (p = 0.039) accompanied by a larger quantity HBsAg (p = 0.045) and HBcAg (p = 0.006) in the liver. We conclude that prednisolone causes immunosuppression permitting enhanced viral multiplication and leads to increased erosion of the limiting plate. Our result also indicates that progression to cirrhosis is unhalted by prednisolone therapy. The histologic findings support clinico-biochemical conclusion that the use of prednisolone is deleterious to patients with HBsAg-positive chronic active hepatitis. | en_US |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ | en_US |
dc.relation.ispartof | Hepatology | en_US |
dc.subject.mesh | Biopsy | en_US |
dc.subject.mesh | Hepatitis B Core Antigens - Analysis | en_US |
dc.subject.mesh | Hepatitis B Surface Antigens | en_US |
dc.subject.mesh | Hepatitis, Chronic - Drug Therapy - Pathology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Liver - Pathology | en_US |
dc.subject.mesh | Liver Regeneration | en_US |
dc.subject.mesh | Prednisolone - Adverse Effects | en_US |
dc.subject.mesh | Prospective Studies | en_US |
dc.title | Prednisolone in HBsAg-positive chronic active hepatitis: Histologic evaluation in a controlled prospective study | 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 | 10.1002/hep.1840020605 | - |
dc.identifier.pmid | 7141388 | - |
dc.identifier.scopus | eid_2-s2.0-0020373510 | en_US |
dc.identifier.volume | 2 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.spage | 777 | en_US |
dc.identifier.epage | 783 | en_US |
dc.identifier.isi | WOS:A1982PS02600004 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Wu, PC=7403119323 | en_US |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_US |
dc.identifier.scopusauthorid | Lam, KC=7403657286 | en_US |
dc.identifier.scopusauthorid | Ho, J=7402649982 | en_US |
dc.identifier.issnl | 0270-9139 | - |