Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil

Detalhes bibliográficos
Autor(a) principal: Santos,Damião Carlos Moraes dos
Data de Publicação: 2009
Outros Autores: Martinho,José Manoel da Silva Gomes, Pacheco-Moreira,Lucio Filgueiras, Araújo,Cristina Carvalho Viana de, Oliveira,Barbara Cristina Euzebio Pereira Dias de, Lago,Barbara Vieira, Pinto,Marcelo Alves, Paula,Vanessa Salete de
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Brazilian Journal of Infectious Diseases
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702009000500002
Resumo: Fulminant hepatic failure (FHF) is characterized by massive hepatocellular injury, whose physiopathology is still unclear. Hepatitis B (HBV) is probably the most common viral cause of FHF, while hepatitis A (HAV) virus seem occurs less frequently. However, the host and viral factors that determine the outcome of these infections are poorly understood. In the present study, viral load and genotyping determining regions of HAV and HBV genomes were sequenced. Eight FHF patients and one patient with severe acute hepatitis (SAH) were included. Liver and blood samples were collected during liver transplantation or necropsy procedures. HAV-RNA and HBV-DNA were extracted from serum, biopsy and paraffin liver. Nucleotide sequencing of HAV-RNA was performed from VP1/2A and HBV-DNA from PreS/S region. The amplified samples were quantified by Real-Time PCR. The cases of HAV infection were due to subgenotype IA. The cases of HBV infection were due to genotype A2 and D4. The case of HAV/HBV coinfection was infected by genotype IA and D3. Hepatitis A and B infection were associated with genotypes most prevalent in Brazil. In hepatitis A infection the mean of period evolution was 13 days. In hepatitis B, FHF patients infected by genotype D have a shorter period of evolution than FHF patients infected by genotype A (mean 15 v. 53 days). There was no association with genotype-determining region with the severity of hepatitis, however nucleotide differences and high viral load could be observed among FHF.
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spelling Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, BrazilFulminant hepatitis failurehepatitis A virus (HAV)hepatitis B virus (HBV) and genotype and viral loadFulminant hepatic failure (FHF) is characterized by massive hepatocellular injury, whose physiopathology is still unclear. Hepatitis B (HBV) is probably the most common viral cause of FHF, while hepatitis A (HAV) virus seem occurs less frequently. However, the host and viral factors that determine the outcome of these infections are poorly understood. In the present study, viral load and genotyping determining regions of HAV and HBV genomes were sequenced. Eight FHF patients and one patient with severe acute hepatitis (SAH) were included. Liver and blood samples were collected during liver transplantation or necropsy procedures. HAV-RNA and HBV-DNA were extracted from serum, biopsy and paraffin liver. Nucleotide sequencing of HAV-RNA was performed from VP1/2A and HBV-DNA from PreS/S region. The amplified samples were quantified by Real-Time PCR. The cases of HAV infection were due to subgenotype IA. The cases of HBV infection were due to genotype A2 and D4. The case of HAV/HBV coinfection was infected by genotype IA and D3. Hepatitis A and B infection were associated with genotypes most prevalent in Brazil. In hepatitis A infection the mean of period evolution was 13 days. In hepatitis B, FHF patients infected by genotype D have a shorter period of evolution than FHF patients infected by genotype A (mean 15 v. 53 days). There was no association with genotype-determining region with the severity of hepatitis, however nucleotide differences and high viral load could be observed among FHF.Brazilian Society of Infectious Diseases2009-10-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702009000500002Brazilian Journal of Infectious Diseases v.13 n.5 2009reponame:Brazilian Journal of Infectious Diseasesinstname:Brazilian Society of Infectious Diseases (BSID)instacron:BSID10.1590/S1413-86702009000500002info:eu-repo/semantics/openAccessSantos,Damião Carlos Moraes dosMartinho,José Manoel da Silva GomesPacheco-Moreira,Lucio FilgueirasAraújo,Cristina Carvalho Viana deOliveira,Barbara Cristina Euzebio Pereira Dias deLago,Barbara VieiraPinto,Marcelo AlvesPaula,Vanessa Salete deeng2010-04-14T00:00:00Zoai:scielo:S1413-86702009000500002Revistahttps://www.bjid.org.br/https://old.scielo.br/oai/scielo-oai.phpbjid@bjid.org.br||lgoldani@ufrgs.br1678-43911413-8670opendoar:2010-04-14T00:00Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)false
dc.title.none.fl_str_mv Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
title Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
spellingShingle Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
Santos,Damião Carlos Moraes dos
Fulminant hepatitis failure
hepatitis A virus (HAV)
hepatitis B virus (HBV) and genotype and viral load
title_short Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
title_full Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
title_fullStr Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
title_full_unstemmed Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
title_sort Fulminant hepatitis failure in adults and children from a Public Hospital in Rio de Janeiro, Brazil
author Santos,Damião Carlos Moraes dos
author_facet Santos,Damião Carlos Moraes dos
Martinho,José Manoel da Silva Gomes
Pacheco-Moreira,Lucio Filgueiras
Araújo,Cristina Carvalho Viana de
Oliveira,Barbara Cristina Euzebio Pereira Dias de
Lago,Barbara Vieira
Pinto,Marcelo Alves
Paula,Vanessa Salete de
author_role author
author2 Martinho,José Manoel da Silva Gomes
Pacheco-Moreira,Lucio Filgueiras
Araújo,Cristina Carvalho Viana de
Oliveira,Barbara Cristina Euzebio Pereira Dias de
Lago,Barbara Vieira
Pinto,Marcelo Alves
Paula,Vanessa Salete de
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Santos,Damião Carlos Moraes dos
Martinho,José Manoel da Silva Gomes
Pacheco-Moreira,Lucio Filgueiras
Araújo,Cristina Carvalho Viana de
Oliveira,Barbara Cristina Euzebio Pereira Dias de
Lago,Barbara Vieira
Pinto,Marcelo Alves
Paula,Vanessa Salete de
dc.subject.por.fl_str_mv Fulminant hepatitis failure
hepatitis A virus (HAV)
hepatitis B virus (HBV) and genotype and viral load
topic Fulminant hepatitis failure
hepatitis A virus (HAV)
hepatitis B virus (HBV) and genotype and viral load
description Fulminant hepatic failure (FHF) is characterized by massive hepatocellular injury, whose physiopathology is still unclear. Hepatitis B (HBV) is probably the most common viral cause of FHF, while hepatitis A (HAV) virus seem occurs less frequently. However, the host and viral factors that determine the outcome of these infections are poorly understood. In the present study, viral load and genotyping determining regions of HAV and HBV genomes were sequenced. Eight FHF patients and one patient with severe acute hepatitis (SAH) were included. Liver and blood samples were collected during liver transplantation or necropsy procedures. HAV-RNA and HBV-DNA were extracted from serum, biopsy and paraffin liver. Nucleotide sequencing of HAV-RNA was performed from VP1/2A and HBV-DNA from PreS/S region. The amplified samples were quantified by Real-Time PCR. The cases of HAV infection were due to subgenotype IA. The cases of HBV infection were due to genotype A2 and D4. The case of HAV/HBV coinfection was infected by genotype IA and D3. Hepatitis A and B infection were associated with genotypes most prevalent in Brazil. In hepatitis A infection the mean of period evolution was 13 days. In hepatitis B, FHF patients infected by genotype D have a shorter period of evolution than FHF patients infected by genotype A (mean 15 v. 53 days). There was no association with genotype-determining region with the severity of hepatitis, however nucleotide differences and high viral load could be observed among FHF.
publishDate 2009
dc.date.none.fl_str_mv 2009-10-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702009000500002
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702009000500002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1413-86702009000500002
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
dc.source.none.fl_str_mv Brazilian Journal of Infectious Diseases v.13 n.5 2009
reponame:Brazilian Journal of Infectious Diseases
instname:Brazilian Society of Infectious Diseases (BSID)
instacron:BSID
instname_str Brazilian Society of Infectious Diseases (BSID)
instacron_str BSID
institution BSID
reponame_str Brazilian Journal of Infectious Diseases
collection Brazilian Journal of Infectious Diseases
repository.name.fl_str_mv Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)
repository.mail.fl_str_mv bjid@bjid.org.br||lgoldani@ufrgs.br
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