Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus

Detalhes bibliográficos
Autor(a) principal: Aikawa,Nádia E.
Data de Publicação: 2016
Outros Autores: Nascimento,Ana P., Hayata,André L.S., Bonfá,Eloisa, Goldenstein-Schainberg,Cláudia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Brasileira de Reumatologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0482-50042016000300235
Resumo: Abstract Objective To evaluate the prevalence of hepatitis C virus (HCV) infection in high risk juvenile systemic lupus erythematosus (JSLE). Study design Forty low income JSLE patients (6M:34F; mean age 19 ± 4.4 yrs; mean disease duration 6 ± 3.2 yrs) were studied. Twenty healthy children and adolescents matched for social economical level were included as controls. Anti-HCV tests were performed using a third generation microparticle enzyme immunoassay. Inclusion criterion was low social economical level. Results The frequencies of anti-HCV antibody were low and comparable between JSLE and control group (2.5% vs. 0, p = 1.0). JSLE patients had significantly more risk factors for HCV infection compared to the control group, including immunosuppressive treatment (90% vs. 0, p < 0.0001), hospitalization (50% vs. 12.5%, p = 0.0006) and invasive procedures (47.5% vs. 12.5%, p = 0.001). Conclusions The observed low frequency of anti-HCV antibodies in high risk JSLE suggests that this virus does not seem to have a relevant role in the pathogenesis of this disease.
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spelling Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosusHepatitis C virusAnti-HCVJuvenile systemic lupus erythematosusAbstract Objective To evaluate the prevalence of hepatitis C virus (HCV) infection in high risk juvenile systemic lupus erythematosus (JSLE). Study design Forty low income JSLE patients (6M:34F; mean age 19 ± 4.4 yrs; mean disease duration 6 ± 3.2 yrs) were studied. Twenty healthy children and adolescents matched for social economical level were included as controls. Anti-HCV tests were performed using a third generation microparticle enzyme immunoassay. Inclusion criterion was low social economical level. Results The frequencies of anti-HCV antibody were low and comparable between JSLE and control group (2.5% vs. 0, p = 1.0). JSLE patients had significantly more risk factors for HCV infection compared to the control group, including immunosuppressive treatment (90% vs. 0, p < 0.0001), hospitalization (50% vs. 12.5%, p = 0.0006) and invasive procedures (47.5% vs. 12.5%, p = 0.001). Conclusions The observed low frequency of anti-HCV antibodies in high risk JSLE suggests that this virus does not seem to have a relevant role in the pathogenesis of this disease.Sociedade Brasileira de Reumatologia2016-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0482-50042016000300235Revista Brasileira de Reumatologia v.56 n.3 2016reponame:Revista Brasileira de Reumatologia (Online)instname:Sociedade Brasileira de Reumatologia (SBR)instacron:SBR10.1016/j.rbre.2016.02.011info:eu-repo/semantics/openAccessAikawa,Nádia E.Nascimento,Ana P.Hayata,André L.S.Bonfá,EloisaGoldenstein-Schainberg,Cláudiaeng2016-06-23T00:00:00Zoai:scielo:S0482-50042016000300235Revistahttp://www.scielo.br/scielo.php?script=sci_serial&pid=0482-5004&lng=pt&nrm=isoONGhttps://old.scielo.br/oai/scielo-oai.php||sbre@terra.com.br1809-45700482-5004opendoar:2016-06-23T00:00Revista Brasileira de Reumatologia (Online) - Sociedade Brasileira de Reumatologia (SBR)false
dc.title.none.fl_str_mv Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
title Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
spellingShingle Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
Aikawa,Nádia E.
Hepatitis C virus
Anti-HCV
Juvenile systemic lupus erythematosus
title_short Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
title_full Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
title_fullStr Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
title_full_unstemmed Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
title_sort Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
author Aikawa,Nádia E.
author_facet Aikawa,Nádia E.
Nascimento,Ana P.
Hayata,André L.S.
Bonfá,Eloisa
Goldenstein-Schainberg,Cláudia
author_role author
author2 Nascimento,Ana P.
Hayata,André L.S.
Bonfá,Eloisa
Goldenstein-Schainberg,Cláudia
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Aikawa,Nádia E.
Nascimento,Ana P.
Hayata,André L.S.
Bonfá,Eloisa
Goldenstein-Schainberg,Cláudia
dc.subject.por.fl_str_mv Hepatitis C virus
Anti-HCV
Juvenile systemic lupus erythematosus
topic Hepatitis C virus
Anti-HCV
Juvenile systemic lupus erythematosus
description Abstract Objective To evaluate the prevalence of hepatitis C virus (HCV) infection in high risk juvenile systemic lupus erythematosus (JSLE). Study design Forty low income JSLE patients (6M:34F; mean age 19 ± 4.4 yrs; mean disease duration 6 ± 3.2 yrs) were studied. Twenty healthy children and adolescents matched for social economical level were included as controls. Anti-HCV tests were performed using a third generation microparticle enzyme immunoassay. Inclusion criterion was low social economical level. Results The frequencies of anti-HCV antibody were low and comparable between JSLE and control group (2.5% vs. 0, p = 1.0). JSLE patients had significantly more risk factors for HCV infection compared to the control group, including immunosuppressive treatment (90% vs. 0, p < 0.0001), hospitalization (50% vs. 12.5%, p = 0.0006) and invasive procedures (47.5% vs. 12.5%, p = 0.001). Conclusions The observed low frequency of anti-HCV antibodies in high risk JSLE suggests that this virus does not seem to have a relevant role in the pathogenesis of this disease.
publishDate 2016
dc.date.none.fl_str_mv 2016-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0482-50042016000300235
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.rbre.2016.02.011
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Reumatologia
publisher.none.fl_str_mv Sociedade Brasileira de Reumatologia
dc.source.none.fl_str_mv Revista Brasileira de Reumatologia v.56 n.3 2016
reponame:Revista Brasileira de Reumatologia (Online)
instname:Sociedade Brasileira de Reumatologia (SBR)
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