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The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis()

BACKGROUND/AIMS: Although there have been a few reports regarding the effect of basal core promoter (BCP) double mutations (A1762T and G1764A) on hepatitis B viral loads, the association remains uncertain. We aim to determine the association after controlling for HBeAg – a strong confounding factor....

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Autores principales: Fang, Zhong-Liao, Sabin, Caroline A, Dong, Bai-Qing, Wei, Shao-Chao, Chen, Qin-Yan, Fang, Kong-Xiong, Yang, Jin-Ye, Wang, Xue-Yan, Harrison, Tim J.
Formato: Texto
Lenguaje:English
Publicado: Elsevier 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648871/
https://www.ncbi.nlm.nih.gov/pubmed/19070921
http://dx.doi.org/10.1016/j.jhep.2008.09.014
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author Fang, Zhong-Liao
Sabin, Caroline A
Dong, Bai-Qing
Wei, Shao-Chao
Chen, Qin-Yan
Fang, Kong-Xiong
Yang, Jin-Ye
Wang, Xue-Yan
Harrison, Tim J.
author_facet Fang, Zhong-Liao
Sabin, Caroline A
Dong, Bai-Qing
Wei, Shao-Chao
Chen, Qin-Yan
Fang, Kong-Xiong
Yang, Jin-Ye
Wang, Xue-Yan
Harrison, Tim J.
author_sort Fang, Zhong-Liao
collection PubMed
description BACKGROUND/AIMS: Although there have been a few reports regarding the effect of basal core promoter (BCP) double mutations (A1762T and G1764A) on hepatitis B viral loads, the association remains uncertain. We aim to determine the association after controlling for HBeAg – a strong confounding factor. METHODS: We selected randomly 190 individuals from a Chinese cohort of 2258 subjects for cross-sectional analysis and 56 of the 190 for longitudinal analysis of viral loads. RESULTS: In multivariable analysis of the cross-sectional data, BCP double mutations are significantly associated with lower viral loads in HBeAg positive subjects but no difference was found in anti-HBe positive subjects. Triple mutations at nucleotide (nt) 1753, 1762 and 1764 and mutations between nt 1809 and 1817, precore stop mutation (nt 1896) and genotype are not associated with viral loads in either HBeAg or anti-HBe positive subjects. Analysis of the longitudinal data yielded similar results to the cross-sectional data. Viral loads differ significantly between individuals infected with wild-type and BCP double mutations prior to HBeAg seroconversion but this difference is lost after seroconversion. CONCLUSIONS: BCP double mutations are associated with lower viral loads in HBeAg positive individuals but have no effect on the viral loads of anti-HBe positive individuals.
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spelling pubmed-26488712009-04-15 The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis() Fang, Zhong-Liao Sabin, Caroline A Dong, Bai-Qing Wei, Shao-Chao Chen, Qin-Yan Fang, Kong-Xiong Yang, Jin-Ye Wang, Xue-Yan Harrison, Tim J. J Hepatol Article BACKGROUND/AIMS: Although there have been a few reports regarding the effect of basal core promoter (BCP) double mutations (A1762T and G1764A) on hepatitis B viral loads, the association remains uncertain. We aim to determine the association after controlling for HBeAg – a strong confounding factor. METHODS: We selected randomly 190 individuals from a Chinese cohort of 2258 subjects for cross-sectional analysis and 56 of the 190 for longitudinal analysis of viral loads. RESULTS: In multivariable analysis of the cross-sectional data, BCP double mutations are significantly associated with lower viral loads in HBeAg positive subjects but no difference was found in anti-HBe positive subjects. Triple mutations at nucleotide (nt) 1753, 1762 and 1764 and mutations between nt 1809 and 1817, precore stop mutation (nt 1896) and genotype are not associated with viral loads in either HBeAg or anti-HBe positive subjects. Analysis of the longitudinal data yielded similar results to the cross-sectional data. Viral loads differ significantly between individuals infected with wild-type and BCP double mutations prior to HBeAg seroconversion but this difference is lost after seroconversion. CONCLUSIONS: BCP double mutations are associated with lower viral loads in HBeAg positive individuals but have no effect on the viral loads of anti-HBe positive individuals. Elsevier 2009-02 /pmc/articles/PMC2648871/ /pubmed/19070921 http://dx.doi.org/10.1016/j.jhep.2008.09.014 Text en © 2009 Elsevier B.V. https://creativecommons.org/licenses/by/4.0/ Open Access under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) license
spellingShingle Article
Fang, Zhong-Liao
Sabin, Caroline A
Dong, Bai-Qing
Wei, Shao-Chao
Chen, Qin-Yan
Fang, Kong-Xiong
Yang, Jin-Ye
Wang, Xue-Yan
Harrison, Tim J.
The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis()
title The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis()
title_full The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis()
title_fullStr The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis()
title_full_unstemmed The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis()
title_short The association of HBV core promoter double mutations (A1762T and G1764A) with viral load differs between HBeAg positive and anti-HBe positive individuals: A longitudinal analysis()
title_sort association of hbv core promoter double mutations (a1762t and g1764a) with viral load differs between hbeag positive and anti-hbe positive individuals: a longitudinal analysis()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648871/
https://www.ncbi.nlm.nih.gov/pubmed/19070921
http://dx.doi.org/10.1016/j.jhep.2008.09.014
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