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Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV
BACKGROUND: Patients co-infected with hepatitis B virus (HBV) and the human immunodeficiency virus (HIV) are at risk of developing hepatocellular carcinoma (HCC). In sub-Saharan Africa, the overlap between high HIV and HBV prevalence may increase the incidence of HCC. This study investigated the imp...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359588/ https://www.ncbi.nlm.nih.gov/pubmed/32660431 http://dx.doi.org/10.1186/s12876-020-01372-2 |
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author | Maponga, Tongai Gibson Glashoff, Richard H. Vermeulen, Hannali Robertson, Barbara Burmeister, Sean Bernon, Marc Omoshoro-Jones, Jones Ruff, Paul Neugut, Alfred I. Jacobson, Judith S. Preiser, Wolfgang Andersson, Monique I. |
author_facet | Maponga, Tongai Gibson Glashoff, Richard H. Vermeulen, Hannali Robertson, Barbara Burmeister, Sean Bernon, Marc Omoshoro-Jones, Jones Ruff, Paul Neugut, Alfred I. Jacobson, Judith S. Preiser, Wolfgang Andersson, Monique I. |
author_sort | Maponga, Tongai Gibson |
collection | PubMed |
description | BACKGROUND: Patients co-infected with hepatitis B virus (HBV) and the human immunodeficiency virus (HIV) are at risk of developing hepatocellular carcinoma (HCC). In sub-Saharan Africa, the overlap between high HIV and HBV prevalence may increase the incidence of HCC. This study investigated the impact of HBV/HIV co-infection on age at presentation and survival of HCC. METHODS: Ethical approval was obtained to recruit, following informed written consent, patients diagnosed with HCC at oncology units at four South African hospitals. Between December 2012 and August 2015, patients newly diagnosed with HCC were recruited and provided demographic and clinical data and blood specimens. Patients were tested for HBV, hepatitis C virus (HCV) and HIV. Survival data was available for a subset of patients. RESULTS: Of 107 HCC cases, 83 (78%) were male. Median age was 46 years (range 18 to 90 years), 68/106 (64%) were HBsAg-positive, and 22/100 (22%) were HIV infected. Among HBV surface antigen (HBsAg)-positive HCC cases, 18/66 (27%) were HIV-infected compared to 3/34 (9%) among those that were HBsAg-negative (p = 0.04). A greater proportion of HBV/HIV co-infected cases were female than HBV mono-infected (6/18, 33% vs 6/47, 13%; p = 0.005). In addition, HBV/HIV co-infected females presented at a younger mean age (36.8 years) than HBV mono-infected women (50.5 years) (p = 0.09). Median survival was 82 days among the HIV-infected HCC patients compared to 181 days among those without HIV (p = 0.15). CONCLUSIONS: HCC is an important complication in the HIV/HBV infected patient. HIV-positive patients presented with HCC at a younger age than HIV-negative patients, this effect appears to be greater in women. These data provide more evidence supporting the call to address. HCC as a cause of morbidity and mortality in the HBV/HIV co-infected patient population. (281 words). |
format | Online Article Text |
id | pubmed-7359588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73595882020-07-17 Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV Maponga, Tongai Gibson Glashoff, Richard H. Vermeulen, Hannali Robertson, Barbara Burmeister, Sean Bernon, Marc Omoshoro-Jones, Jones Ruff, Paul Neugut, Alfred I. Jacobson, Judith S. Preiser, Wolfgang Andersson, Monique I. BMC Gastroenterol Research Article BACKGROUND: Patients co-infected with hepatitis B virus (HBV) and the human immunodeficiency virus (HIV) are at risk of developing hepatocellular carcinoma (HCC). In sub-Saharan Africa, the overlap between high HIV and HBV prevalence may increase the incidence of HCC. This study investigated the impact of HBV/HIV co-infection on age at presentation and survival of HCC. METHODS: Ethical approval was obtained to recruit, following informed written consent, patients diagnosed with HCC at oncology units at four South African hospitals. Between December 2012 and August 2015, patients newly diagnosed with HCC were recruited and provided demographic and clinical data and blood specimens. Patients were tested for HBV, hepatitis C virus (HCV) and HIV. Survival data was available for a subset of patients. RESULTS: Of 107 HCC cases, 83 (78%) were male. Median age was 46 years (range 18 to 90 years), 68/106 (64%) were HBsAg-positive, and 22/100 (22%) were HIV infected. Among HBV surface antigen (HBsAg)-positive HCC cases, 18/66 (27%) were HIV-infected compared to 3/34 (9%) among those that were HBsAg-negative (p = 0.04). A greater proportion of HBV/HIV co-infected cases were female than HBV mono-infected (6/18, 33% vs 6/47, 13%; p = 0.005). In addition, HBV/HIV co-infected females presented at a younger mean age (36.8 years) than HBV mono-infected women (50.5 years) (p = 0.09). Median survival was 82 days among the HIV-infected HCC patients compared to 181 days among those without HIV (p = 0.15). CONCLUSIONS: HCC is an important complication in the HIV/HBV infected patient. HIV-positive patients presented with HCC at a younger age than HIV-negative patients, this effect appears to be greater in women. These data provide more evidence supporting the call to address. HCC as a cause of morbidity and mortality in the HBV/HIV co-infected patient population. (281 words). BioMed Central 2020-07-13 /pmc/articles/PMC7359588/ /pubmed/32660431 http://dx.doi.org/10.1186/s12876-020-01372-2 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Maponga, Tongai Gibson Glashoff, Richard H. Vermeulen, Hannali Robertson, Barbara Burmeister, Sean Bernon, Marc Omoshoro-Jones, Jones Ruff, Paul Neugut, Alfred I. Jacobson, Judith S. Preiser, Wolfgang Andersson, Monique I. Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV |
title | Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV |
title_full | Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV |
title_fullStr | Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV |
title_full_unstemmed | Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV |
title_short | Hepatitis B virus-associated hepatocellular carcinoma in South Africa in the era of HIV |
title_sort | hepatitis b virus-associated hepatocellular carcinoma in south africa in the era of hiv |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359588/ https://www.ncbi.nlm.nih.gov/pubmed/32660431 http://dx.doi.org/10.1186/s12876-020-01372-2 |
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