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Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil

Infection by hepatitis B virus (HBV) is a worldwide public health problem. Chronic HBV infection with high viral replication may lead to cirrhosis and/or hepatocellular carcinoma. Mutant HBV strains, such as the HBV A1762T/G1764A double mutant, have been associated with poor prognosis and higher ris...

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Autores principales: Silva Souza, Adaliany Cecília da, Souza Marasca, Giórgia de, Kretzmann-Filho, Nélson Alexandre, Dall-Bello, Aline, Alexandre Kliemann, Dimas, Valle Tovo, Cristiane, Gorini da Veiga, Ana Beatriz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425463/
https://www.ncbi.nlm.nih.gov/pubmed/28606415
http://dx.doi.org/10.1016/j.bjid.2017.05.002
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author Silva Souza, Adaliany Cecília da
Souza Marasca, Giórgia de
Kretzmann-Filho, Nélson Alexandre
Dall-Bello, Aline
Alexandre Kliemann, Dimas
Valle Tovo, Cristiane
Gorini da Veiga, Ana Beatriz
author_facet Silva Souza, Adaliany Cecília da
Souza Marasca, Giórgia de
Kretzmann-Filho, Nélson Alexandre
Dall-Bello, Aline
Alexandre Kliemann, Dimas
Valle Tovo, Cristiane
Gorini da Veiga, Ana Beatriz
author_sort Silva Souza, Adaliany Cecília da
collection PubMed
description Infection by hepatitis B virus (HBV) is a worldwide public health problem. Chronic HBV infection with high viral replication may lead to cirrhosis and/or hepatocellular carcinoma. Mutant HBV strains, such as the HBV A1762T/G1764A double mutant, have been associated with poor prognosis and higher risk of the patient for developing cirrhosis and/or hepatocellular carcinoma. This study analyzed the presence of the HBV A1762T/G1764A double mutant in patients with chronic HBV and its association with clinical parameters such as viral load, aminotransferases, and HBV antigens. A total of 49 patients with chronic hepatitis B were included in the study, and the HBV A1762T/G1764A double mutant strain was detected in four samples (8.16%) by polymerase chain reaction followed by restriction fragment length analysis (PCR-RFLP). The viral load was not significantly different between patients with or without the double mutant strain (p = 0.43). On the other hand, carriers of the HBV A1762T/G1764A double mutant had higher levels of ALT (p = 0.0028), while AST levels did not differ between groups (p = 0.051). In this study, 75% of the samples with the HBV A1762T/G1764A double mutation were HBeAg negative and anti-HBe positive, reflecting seroconversion even though they still displayed high viral loads. Our study has shown that the HBV A1762T/G1764A double mutant strain circulates in Brazilian patients, and is associated with elevated levels of ALT and HBeAg seroconversion.
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spelling pubmed-94254632022-08-31 Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil Silva Souza, Adaliany Cecília da Souza Marasca, Giórgia de Kretzmann-Filho, Nélson Alexandre Dall-Bello, Aline Alexandre Kliemann, Dimas Valle Tovo, Cristiane Gorini da Veiga, Ana Beatriz Braz J Infect Dis Original Article Infection by hepatitis B virus (HBV) is a worldwide public health problem. Chronic HBV infection with high viral replication may lead to cirrhosis and/or hepatocellular carcinoma. Mutant HBV strains, such as the HBV A1762T/G1764A double mutant, have been associated with poor prognosis and higher risk of the patient for developing cirrhosis and/or hepatocellular carcinoma. This study analyzed the presence of the HBV A1762T/G1764A double mutant in patients with chronic HBV and its association with clinical parameters such as viral load, aminotransferases, and HBV antigens. A total of 49 patients with chronic hepatitis B were included in the study, and the HBV A1762T/G1764A double mutant strain was detected in four samples (8.16%) by polymerase chain reaction followed by restriction fragment length analysis (PCR-RFLP). The viral load was not significantly different between patients with or without the double mutant strain (p = 0.43). On the other hand, carriers of the HBV A1762T/G1764A double mutant had higher levels of ALT (p = 0.0028), while AST levels did not differ between groups (p = 0.051). In this study, 75% of the samples with the HBV A1762T/G1764A double mutation were HBeAg negative and anti-HBe positive, reflecting seroconversion even though they still displayed high viral loads. Our study has shown that the HBV A1762T/G1764A double mutant strain circulates in Brazilian patients, and is associated with elevated levels of ALT and HBeAg seroconversion. Elsevier 2017-06-09 /pmc/articles/PMC9425463/ /pubmed/28606415 http://dx.doi.org/10.1016/j.bjid.2017.05.002 Text en © 2017 Sociedade Brasileira de Infectologia. Published by Elsevier Editora Ltda. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Silva Souza, Adaliany Cecília da
Souza Marasca, Giórgia de
Kretzmann-Filho, Nélson Alexandre
Dall-Bello, Aline
Alexandre Kliemann, Dimas
Valle Tovo, Cristiane
Gorini da Veiga, Ana Beatriz
Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil
title Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil
title_full Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil
title_fullStr Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil
title_full_unstemmed Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil
title_short Identification of hepatitis B virus A1762T/G1764A double mutant strain in patients in Southern Brazil
title_sort identification of hepatitis b virus a1762t/g1764a double mutant strain in patients in southern brazil
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425463/
https://www.ncbi.nlm.nih.gov/pubmed/28606415
http://dx.doi.org/10.1016/j.bjid.2017.05.002
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