Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus

Detalhes bibliográficos
Autor(a) principal: Postal, Mariana
Data de Publicação: 2012
Outros Autores: Sinicato, Nailu Angélica, Peliçari, Karina Oliveira, Marini, Roberto, Lavras Costallat, Lilian Tereza, Appenzeller, Simone
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/19682
Resumo: OBJECTIVE: To determine the serum levels of interferon alpha in childhood-onset systemic lupus erythematosus patients, their first-degree relatives and healthy controls and to evaluate the associations between serum interferon alpha and disease activity, laboratory findings and treatment features. METHODS: We screened consecutive childhood-onset systemic lupus erythematosus patients in a longitudinal cohort at the pediatric rheumatology unit of the State University of Campinas between 2009 and 2010. All patients demonstrated disease onset before the age of 16. Disease status was assessed according to the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI). Interferon alpha levels were measured using an enzyme-linked immunoabsorbent assay. RESULTS: We included 57 childhood-onset systemic lupus erythematosus patients (mean age 17.33±4.50), 64 firstdegree relatives (mean age 39.95±5.66), and 57 healthy (mean age 19.30±4.97) controls. Serum interferon alpha levels were significantly increased in childhood-onset systemic lupus erythematosus patients compared to their firstdegree relatives and healthy controls. Interferon alpha levels were significantly increased in patients with positive dsDNA antibodies, patients with cutaneous vasculitis, patients with new malar rash and patients who were not receiving medication. Interferon alpha levels correlated with C3 levels and systemic lupus erythematosus Disease Activity Index scores. In addition, we observed an inverse correlation between patient age and interferon alpha levels. CONCLUSION: Interferon alpha may play a role in the pathogenesis of childhood-onset systemic lupus erythematosus, especially in cutaneous manifestations and dsDNA antibody formation. The observation that interferon alpha levels are increased in patients who are not taking medication should be investigated in longitudinal studies to determine whether elevated interferon alpha levels may predict systemic lupus erythematosus flares.
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spelling Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosusInterferon alpha (IFN-a)SLEDAIChildhood-onsetSystemic lupus erythematosusOBJECTIVE: To determine the serum levels of interferon alpha in childhood-onset systemic lupus erythematosus patients, their first-degree relatives and healthy controls and to evaluate the associations between serum interferon alpha and disease activity, laboratory findings and treatment features. METHODS: We screened consecutive childhood-onset systemic lupus erythematosus patients in a longitudinal cohort at the pediatric rheumatology unit of the State University of Campinas between 2009 and 2010. All patients demonstrated disease onset before the age of 16. Disease status was assessed according to the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI). Interferon alpha levels were measured using an enzyme-linked immunoabsorbent assay. RESULTS: We included 57 childhood-onset systemic lupus erythematosus patients (mean age 17.33±4.50), 64 firstdegree relatives (mean age 39.95±5.66), and 57 healthy (mean age 19.30±4.97) controls. Serum interferon alpha levels were significantly increased in childhood-onset systemic lupus erythematosus patients compared to their firstdegree relatives and healthy controls. Interferon alpha levels were significantly increased in patients with positive dsDNA antibodies, patients with cutaneous vasculitis, patients with new malar rash and patients who were not receiving medication. Interferon alpha levels correlated with C3 levels and systemic lupus erythematosus Disease Activity Index scores. In addition, we observed an inverse correlation between patient age and interferon alpha levels. CONCLUSION: Interferon alpha may play a role in the pathogenesis of childhood-onset systemic lupus erythematosus, especially in cutaneous manifestations and dsDNA antibody formation. The observation that interferon alpha levels are increased in patients who are not taking medication should be investigated in longitudinal studies to determine whether elevated interferon alpha levels may predict systemic lupus erythematosus flares.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/19682DOI:10.6061/clinics/2012(02)11Clinics; Vol. 67 No. 2 (2012); 157-162Clinics; v. 67 n. 2 (2012); 157-162Clinics; Vol. 67 Núm. 2 (2012); 157-1621980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/19682/21746Postal, MarianaSinicato, Nailu AngélicaPeliçari, Karina OliveiraMarini, RobertoLavras Costallat, Lilian TerezaAppenzeller, Simoneinfo:eu-repo/semantics/openAccess2012-05-24T18:50:51Zoai:revistas.usp.br:article/19682Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-24T18:50:51Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
title Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
spellingShingle Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
Postal, Mariana
Interferon alpha (IFN-a)
SLEDAI
Childhood-onset
Systemic lupus erythematosus
title_short Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
title_full Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
title_fullStr Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
title_full_unstemmed Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
title_sort Clinical and serological manifestations associated with interferon-α levels in childhood-onset systemic lupus erythematosus
author Postal, Mariana
author_facet Postal, Mariana
Sinicato, Nailu Angélica
Peliçari, Karina Oliveira
Marini, Roberto
Lavras Costallat, Lilian Tereza
Appenzeller, Simone
author_role author
author2 Sinicato, Nailu Angélica
Peliçari, Karina Oliveira
Marini, Roberto
Lavras Costallat, Lilian Tereza
Appenzeller, Simone
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Postal, Mariana
Sinicato, Nailu Angélica
Peliçari, Karina Oliveira
Marini, Roberto
Lavras Costallat, Lilian Tereza
Appenzeller, Simone
dc.subject.por.fl_str_mv Interferon alpha (IFN-a)
SLEDAI
Childhood-onset
Systemic lupus erythematosus
topic Interferon alpha (IFN-a)
SLEDAI
Childhood-onset
Systemic lupus erythematosus
description OBJECTIVE: To determine the serum levels of interferon alpha in childhood-onset systemic lupus erythematosus patients, their first-degree relatives and healthy controls and to evaluate the associations between serum interferon alpha and disease activity, laboratory findings and treatment features. METHODS: We screened consecutive childhood-onset systemic lupus erythematosus patients in a longitudinal cohort at the pediatric rheumatology unit of the State University of Campinas between 2009 and 2010. All patients demonstrated disease onset before the age of 16. Disease status was assessed according to the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI). Interferon alpha levels were measured using an enzyme-linked immunoabsorbent assay. RESULTS: We included 57 childhood-onset systemic lupus erythematosus patients (mean age 17.33±4.50), 64 firstdegree relatives (mean age 39.95±5.66), and 57 healthy (mean age 19.30±4.97) controls. Serum interferon alpha levels were significantly increased in childhood-onset systemic lupus erythematosus patients compared to their firstdegree relatives and healthy controls. Interferon alpha levels were significantly increased in patients with positive dsDNA antibodies, patients with cutaneous vasculitis, patients with new malar rash and patients who were not receiving medication. Interferon alpha levels correlated with C3 levels and systemic lupus erythematosus Disease Activity Index scores. In addition, we observed an inverse correlation between patient age and interferon alpha levels. CONCLUSION: Interferon alpha may play a role in the pathogenesis of childhood-onset systemic lupus erythematosus, especially in cutaneous manifestations and dsDNA antibody formation. The observation that interferon alpha levels are increased in patients who are not taking medication should be investigated in longitudinal studies to determine whether elevated interferon alpha levels may predict systemic lupus erythematosus flares.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/19682
DOI:10.6061/clinics/2012(02)11
url https://www.revistas.usp.br/clinics/article/view/19682
identifier_str_mv DOI:10.6061/clinics/2012(02)11
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/19682/21746
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 67 No. 2 (2012); 157-162
Clinics; v. 67 n. 2 (2012); 157-162
Clinics; Vol. 67 Núm. 2 (2012); 157-162
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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