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Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia

BACKGROUND: Little is known about changes in hepatitis B viral load (HBV DNA) in relation to age in Africa. The aim of this study is to determine the natural course of HBV chronic infection, particularly in relation to sequential changes in serum HBV DNA levels and hepatitis B surface (HBsAg) antige...

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Autores principales: Mendy, Maimuna E, McConkey, Samuel J, Sande van der, Marianne AB, Crozier, Sarah, Kaye, Steve, Jeffries, David, Hall, Andrew J, Whittle, Hilton C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358882/
https://www.ncbi.nlm.nih.gov/pubmed/18416832
http://dx.doi.org/10.1186/1743-422X-5-49
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author Mendy, Maimuna E
McConkey, Samuel J
Sande van der, Marianne AB
Crozier, Sarah
Kaye, Steve
Jeffries, David
Hall, Andrew J
Whittle, Hilton C
author_facet Mendy, Maimuna E
McConkey, Samuel J
Sande van der, Marianne AB
Crozier, Sarah
Kaye, Steve
Jeffries, David
Hall, Andrew J
Whittle, Hilton C
author_sort Mendy, Maimuna E
collection PubMed
description BACKGROUND: Little is known about changes in hepatitis B viral load (HBV DNA) in relation to age in Africa. The aim of this study is to determine the natural course of HBV chronic infection, particularly in relation to sequential changes in serum HBV DNA levels and hepatitis B surface (HBsAg) antigen/hepatitis e antigen (HBeAg) status by age. METHODS: The study was conducted on 190 HBV chronic carriers, aged 1–19 years who were followed for 19 years. 160, 99 and 123 were traced at 5, 9 and 19 years later. All available samples were tested for HBsAg and HBeAg, whilst 170, 61, 63 and 81 were tested for HBV DNA at the baseline, and at 5, 9 and 19 years following recruitment. RESULTS: In general HBeAg which correlated with high levels of HBV DNA was lost at a much faster rate than HBsAg. 86% of the carriers who were recruited at the age of 1–4 yrs lost HBeAg by the age of 19 years compared to 30% who lost HBsAg. HBeAg negative carriers had serum HBV DNA levels of < 10(5 )copies per mL, HBV DNA positivity declined from 100% in 1–4 yrs old carriers at recruitment to 62.5%,60% and 88% at 5, 9 and 19 years respectively following recruitment. CONCLUSION: After 19 years of follow up, the majority of HBV surface antigen carriers had lost HBeAg positivity and had low levels of viral replication. However small proportions (10–20%) retained HBeAg and continue to have high levels of viral replication.
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spelling pubmed-23588822008-04-29 Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia Mendy, Maimuna E McConkey, Samuel J Sande van der, Marianne AB Crozier, Sarah Kaye, Steve Jeffries, David Hall, Andrew J Whittle, Hilton C Virol J Research BACKGROUND: Little is known about changes in hepatitis B viral load (HBV DNA) in relation to age in Africa. The aim of this study is to determine the natural course of HBV chronic infection, particularly in relation to sequential changes in serum HBV DNA levels and hepatitis B surface (HBsAg) antigen/hepatitis e antigen (HBeAg) status by age. METHODS: The study was conducted on 190 HBV chronic carriers, aged 1–19 years who were followed for 19 years. 160, 99 and 123 were traced at 5, 9 and 19 years later. All available samples were tested for HBsAg and HBeAg, whilst 170, 61, 63 and 81 were tested for HBV DNA at the baseline, and at 5, 9 and 19 years following recruitment. RESULTS: In general HBeAg which correlated with high levels of HBV DNA was lost at a much faster rate than HBsAg. 86% of the carriers who were recruited at the age of 1–4 yrs lost HBeAg by the age of 19 years compared to 30% who lost HBsAg. HBeAg negative carriers had serum HBV DNA levels of < 10(5 )copies per mL, HBV DNA positivity declined from 100% in 1–4 yrs old carriers at recruitment to 62.5%,60% and 88% at 5, 9 and 19 years respectively following recruitment. CONCLUSION: After 19 years of follow up, the majority of HBV surface antigen carriers had lost HBeAg positivity and had low levels of viral replication. However small proportions (10–20%) retained HBeAg and continue to have high levels of viral replication. BioMed Central 2008-04-16 /pmc/articles/PMC2358882/ /pubmed/18416832 http://dx.doi.org/10.1186/1743-422X-5-49 Text en Copyright © 2008 Mendy et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Mendy, Maimuna E
McConkey, Samuel J
Sande van der, Marianne AB
Crozier, Sarah
Kaye, Steve
Jeffries, David
Hall, Andrew J
Whittle, Hilton C
Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia
title Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia
title_full Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia
title_fullStr Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia
title_full_unstemmed Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia
title_short Changes in viral load and HBsAg and HBeAg status with age in HBV chronic carriers in The Gambia
title_sort changes in viral load and hbsag and hbeag status with age in hbv chronic carriers in the gambia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358882/
https://www.ncbi.nlm.nih.gov/pubmed/18416832
http://dx.doi.org/10.1186/1743-422X-5-49
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