Hepatitis C virus antibodies in high risk juvenile onset systemic lupus erythematosus
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , |
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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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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0482-50042016000300235 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0482-50042016000300235 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.rbre.2016.02.011 |
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 |
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) instacron:SBR |
instname_str |
Sociedade Brasileira de Reumatologia (SBR) |
instacron_str |
SBR |
institution |
SBR |
reponame_str |
Revista Brasileira de Reumatologia (Online) |
collection |
Revista Brasileira de Reumatologia (Online) |
repository.name.fl_str_mv |
Revista Brasileira de Reumatologia (Online) - Sociedade Brasileira de Reumatologia (SBR) |
repository.mail.fl_str_mv |
||sbre@terra.com.br |
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1750318051418439680 |