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Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil
BACKGROUND: Hepatitis E virus (HEV) can cause chronic infection with rapid progression to liver cirrhosis in immunocompromised patients. HEV seroprevalence in patients with Schistosoma mansoni in Brazil is unknown. We evaluated the prevalence of past or present HEV infection in schistosomiasis patie...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425348/ https://www.ncbi.nlm.nih.gov/pubmed/27020708 http://dx.doi.org/10.1016/j.bjid.2016.03.001 |
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author | Passos-Castilho, Ana Maria de Sena, Anne Domingues, Ana Lucia Coutinho Lopes-Neto, Edmundo Pessoa Medeiros, Tibério Batista Granato, Celso Francisco Hernandez Ferraz, Maria Lúcia |
author_facet | Passos-Castilho, Ana Maria de Sena, Anne Domingues, Ana Lucia Coutinho Lopes-Neto, Edmundo Pessoa Medeiros, Tibério Batista Granato, Celso Francisco Hernandez Ferraz, Maria Lúcia |
author_sort | Passos-Castilho, Ana Maria |
collection | PubMed |
description | BACKGROUND: Hepatitis E virus (HEV) can cause chronic infection with rapid progression to liver cirrhosis in immunocompromised patients. HEV seroprevalence in patients with Schistosoma mansoni in Brazil is unknown. We evaluated the prevalence of past or present HEV infection in schistosomiasis patients in Recife, Pernambuco, Brazil. A total of 80 patients with Schistosoma mansoni were consecutively enrolled in a cross-sectional study. Serum samples were tested for the presence of anti-HEV IgG antibodies by enzyme immunoassay (Wantai anti-HEV IgG, Beijing, China) and for the presence of HEV RNA using real time reverse transcriptase-polymerase chain reaction with primers targeting the HEV ORF2 and ORF3. Clinical and laboratory tests as well as abdominal ultrasound were performed at the same day of blood collection. RESULTS: Anti-HEV IgG was positive in 18.8% (15/80) of patients with SM. None of the samples tested positive for anti-HEV IgM or HEV-RNA. Patients with anti-HEV IgG positive presented higher levels of alanine aminotranferase (p = 0.048) and gama-glutamil transferase (p = 0.022) when compared to patients without anti-HEV IgG antibodies. CONCLUSION: This study demonstrates that the seroprevalence of HEV is high in patients with Schistosoma mansoni in Northeastern of Brazil. Past HEV infection is associated with higher frequency of liver enzymes abnormalities. HEV infection and its role on the severity of liver disease should be further investigated among patients with Schistosoma mansoni. |
format | Online Article Text |
id | pubmed-9425348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94253482022-08-31 Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil Passos-Castilho, Ana Maria de Sena, Anne Domingues, Ana Lucia Coutinho Lopes-Neto, Edmundo Pessoa Medeiros, Tibério Batista Granato, Celso Francisco Hernandez Ferraz, Maria Lúcia Braz J Infect Dis Original Article BACKGROUND: Hepatitis E virus (HEV) can cause chronic infection with rapid progression to liver cirrhosis in immunocompromised patients. HEV seroprevalence in patients with Schistosoma mansoni in Brazil is unknown. We evaluated the prevalence of past or present HEV infection in schistosomiasis patients in Recife, Pernambuco, Brazil. A total of 80 patients with Schistosoma mansoni were consecutively enrolled in a cross-sectional study. Serum samples were tested for the presence of anti-HEV IgG antibodies by enzyme immunoassay (Wantai anti-HEV IgG, Beijing, China) and for the presence of HEV RNA using real time reverse transcriptase-polymerase chain reaction with primers targeting the HEV ORF2 and ORF3. Clinical and laboratory tests as well as abdominal ultrasound were performed at the same day of blood collection. RESULTS: Anti-HEV IgG was positive in 18.8% (15/80) of patients with SM. None of the samples tested positive for anti-HEV IgM or HEV-RNA. Patients with anti-HEV IgG positive presented higher levels of alanine aminotranferase (p = 0.048) and gama-glutamil transferase (p = 0.022) when compared to patients without anti-HEV IgG antibodies. CONCLUSION: This study demonstrates that the seroprevalence of HEV is high in patients with Schistosoma mansoni in Northeastern of Brazil. Past HEV infection is associated with higher frequency of liver enzymes abnormalities. HEV infection and its role on the severity of liver disease should be further investigated among patients with Schistosoma mansoni. Elsevier 2016-03-26 /pmc/articles/PMC9425348/ /pubmed/27020708 http://dx.doi.org/10.1016/j.bjid.2016.03.001 Text en © 2016 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 Passos-Castilho, Ana Maria de Sena, Anne Domingues, Ana Lucia Coutinho Lopes-Neto, Edmundo Pessoa Medeiros, Tibério Batista Granato, Celso Francisco Hernandez Ferraz, Maria Lúcia Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil |
title | Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil |
title_full | Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil |
title_fullStr | Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil |
title_full_unstemmed | Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil |
title_short | Hepatitis E virus seroprevalence among schistosomiasis patients in Northeastern Brazil |
title_sort | hepatitis e virus seroprevalence among schistosomiasis patients in northeastern brazil |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425348/ https://www.ncbi.nlm.nih.gov/pubmed/27020708 http://dx.doi.org/10.1016/j.bjid.2016.03.001 |
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