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Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults

BACKGROUND: Occult hepatitis B virus (HBV) infection (OBI) is a phase of HBV infection characterised by the presence of HBV DNA in the absence of detectable hepatitis B surface antigen (HBsAg). OBI is of concern in the HIV-infected due to high prevalence and risk of HBV reactivation. The prevalence...

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Autores principales: Salyani, Adil, Shah, Jasmit, Adam, Rodney, Otieno, George, Mbugua, Evelyn, Shah, Reena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787452/
https://www.ncbi.nlm.nih.gov/pubmed/33406137
http://dx.doi.org/10.1371/journal.pone.0244947
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author Salyani, Adil
Shah, Jasmit
Adam, Rodney
Otieno, George
Mbugua, Evelyn
Shah, Reena
author_facet Salyani, Adil
Shah, Jasmit
Adam, Rodney
Otieno, George
Mbugua, Evelyn
Shah, Reena
author_sort Salyani, Adil
collection PubMed
description BACKGROUND: Occult hepatitis B virus (HBV) infection (OBI) is a phase of HBV infection characterised by the presence of HBV DNA in the absence of detectable hepatitis B surface antigen (HBsAg). OBI is of concern in the HIV-infected due to high prevalence and risk of HBV reactivation. The prevalence and clinico-demographic characteristics of OBI in anti-retroviral therapy (ART) naïve HIV infected adults in Kenya is unknown. METHODS: A cross sectional study carried was out at three sites in Kenya. HIV infected ART naïve adults were enrolled and demographic data collected. Blood samples were assayed for HBsAg, HBV DNA, alanine aminotransferase, aspartate aminotransferase, antibodies to hepatitis B surface antigen (anti-HBs) and hepatitis B core antigen (anti-HBc). Data on CD4 count, HIV viral load and platelet count were obtained from medical records. RESULTS: Of 208 patients, 199 (95.7%) did not report HBV vaccination, 196 (94.2%) were HBsAg negative, 119 (57.2%) had no HBV markers, 58 (27.9%) had previous HBV infection (anti-HBc positive) and 11 (5.3%) had OBI. All 11 (100%) OBI patients were anti-HBc positive. OBI patients comprised 19.0% of HBsAg negative, anti-HBc positive patients. There was no difference in clinico-demographic characteristics between the overt HBV, OBI and HBV negative patients. CONCLUSION: This was the first study on OBI in ART naïve HIV infected adults in Kenya. The lower OBI prevalence compared to other sub-Saharan African countries could be attributed to lower HBV exposure. Most patients were HBV unexposed and unimmunized, outlining the need to implement guideline recommended immunization strategies.
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spelling pubmed-77874522021-01-14 Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults Salyani, Adil Shah, Jasmit Adam, Rodney Otieno, George Mbugua, Evelyn Shah, Reena PLoS One Research Article BACKGROUND: Occult hepatitis B virus (HBV) infection (OBI) is a phase of HBV infection characterised by the presence of HBV DNA in the absence of detectable hepatitis B surface antigen (HBsAg). OBI is of concern in the HIV-infected due to high prevalence and risk of HBV reactivation. The prevalence and clinico-demographic characteristics of OBI in anti-retroviral therapy (ART) naïve HIV infected adults in Kenya is unknown. METHODS: A cross sectional study carried was out at three sites in Kenya. HIV infected ART naïve adults were enrolled and demographic data collected. Blood samples were assayed for HBsAg, HBV DNA, alanine aminotransferase, aspartate aminotransferase, antibodies to hepatitis B surface antigen (anti-HBs) and hepatitis B core antigen (anti-HBc). Data on CD4 count, HIV viral load and platelet count were obtained from medical records. RESULTS: Of 208 patients, 199 (95.7%) did not report HBV vaccination, 196 (94.2%) were HBsAg negative, 119 (57.2%) had no HBV markers, 58 (27.9%) had previous HBV infection (anti-HBc positive) and 11 (5.3%) had OBI. All 11 (100%) OBI patients were anti-HBc positive. OBI patients comprised 19.0% of HBsAg negative, anti-HBc positive patients. There was no difference in clinico-demographic characteristics between the overt HBV, OBI and HBV negative patients. CONCLUSION: This was the first study on OBI in ART naïve HIV infected adults in Kenya. The lower OBI prevalence compared to other sub-Saharan African countries could be attributed to lower HBV exposure. Most patients were HBV unexposed and unimmunized, outlining the need to implement guideline recommended immunization strategies. Public Library of Science 2021-01-06 /pmc/articles/PMC7787452/ /pubmed/33406137 http://dx.doi.org/10.1371/journal.pone.0244947 Text en © 2021 Salyani et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Salyani, Adil
Shah, Jasmit
Adam, Rodney
Otieno, George
Mbugua, Evelyn
Shah, Reena
Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults
title Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults
title_full Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults
title_fullStr Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults
title_full_unstemmed Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults
title_short Occult hepatitis B virus infection in a Kenyan cohort of HIV infected anti-retroviral therapy naïve adults
title_sort occult hepatitis b virus infection in a kenyan cohort of hiv infected anti-retroviral therapy naïve adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787452/
https://www.ncbi.nlm.nih.gov/pubmed/33406137
http://dx.doi.org/10.1371/journal.pone.0244947
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