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Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease.
The aim of the study was to determine whether past exposure to hepatitis B virus (HBV) influences the risk of the development of hepatocellular carcinoma (HCC) in Japanese patients with chronic liver disease (CLD). We conducted a hospital-based case-control study of 141 HCC patients with CLD and 151...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150336/ https://www.ncbi.nlm.nih.gov/pubmed/9667687 |
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author | Okada, S. Sato, T. Okusaka, T. Ishii, H. Ikeda, M. Nakasuka, H. Kosakamoto, H. Yoshimori, M. Wakabayashi, K. |
author_facet | Okada, S. Sato, T. Okusaka, T. Ishii, H. Ikeda, M. Nakasuka, H. Kosakamoto, H. Yoshimori, M. Wakabayashi, K. |
author_sort | Okada, S. |
collection | PubMed |
description | The aim of the study was to determine whether past exposure to hepatitis B virus (HBV) influences the risk of the development of hepatocellular carcinoma (HCC) in Japanese patients with chronic liver disease (CLD). We conducted a hospital-based case-control study of 141 HCC patients with CLD and 151 controls with CLD but without HCC. Past exposure to HBV was assessed by antibody to hepatitis B core antigen (anti-HBc) positivity. Ninety-two patients (65%) with HCC were anti-HBc positive compared with 65 patients (43%) with CLD alone (P < 0.01). A multivariate analysis using logistic regression modelling revealed that anti-HBc positivity significantly increased the risk of the development of HCC [odds ratio (OR) 2.0, P = 0.01]. In the anti-HBc-positive patients, a significantly increased risk of HCC was seen among the patients positive for anti-HBc alone (OR, 2.6; P < 0.01). However, a significant OR was not obtained among the patients with a transient HBV infection implied by positivity for both antibody to hepatitis B surface antigen and anti-HBc (OR, 1.5; P = 0.48). These results indicate that past exposure to HBV is a risk factor for HCC in Japanese CLD patients, especially when they have no serological evidence of immunity to HBV. |
format | Text |
id | pubmed-2150336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-21503362009-09-10 Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. Okada, S. Sato, T. Okusaka, T. Ishii, H. Ikeda, M. Nakasuka, H. Kosakamoto, H. Yoshimori, M. Wakabayashi, K. Br J Cancer Research Article The aim of the study was to determine whether past exposure to hepatitis B virus (HBV) influences the risk of the development of hepatocellular carcinoma (HCC) in Japanese patients with chronic liver disease (CLD). We conducted a hospital-based case-control study of 141 HCC patients with CLD and 151 controls with CLD but without HCC. Past exposure to HBV was assessed by antibody to hepatitis B core antigen (anti-HBc) positivity. Ninety-two patients (65%) with HCC were anti-HBc positive compared with 65 patients (43%) with CLD alone (P < 0.01). A multivariate analysis using logistic regression modelling revealed that anti-HBc positivity significantly increased the risk of the development of HCC [odds ratio (OR) 2.0, P = 0.01]. In the anti-HBc-positive patients, a significantly increased risk of HCC was seen among the patients positive for anti-HBc alone (OR, 2.6; P < 0.01). However, a significant OR was not obtained among the patients with a transient HBV infection implied by positivity for both antibody to hepatitis B surface antigen and anti-HBc (OR, 1.5; P = 0.48). These results indicate that past exposure to HBV is a risk factor for HCC in Japanese CLD patients, especially when they have no serological evidence of immunity to HBV. Nature Publishing Group 1998-06 /pmc/articles/PMC2150336/ /pubmed/9667687 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Okada, S. Sato, T. Okusaka, T. Ishii, H. Ikeda, M. Nakasuka, H. Kosakamoto, H. Yoshimori, M. Wakabayashi, K. Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. |
title | Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. |
title_full | Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. |
title_fullStr | Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. |
title_full_unstemmed | Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. |
title_short | Past exposure to hepatitis B virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. |
title_sort | past exposure to hepatitis b virus as a risk factor for hepatocellular carcinoma in patients with chronic liver disease. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150336/ https://www.ncbi.nlm.nih.gov/pubmed/9667687 |
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