Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings

Detalhes bibliográficos
Autor(a) principal: Dias,Cristiane Bitencourt
Data de Publicação: 2017
Outros Autores: Testagrossa,Leonardo, Jorge,Lectícia, Malheiros,Denise, Woronik,Viktoria
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Jornal Brasileiro de Nefrologia
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000400447
Resumo: Abstract Background: New classification for membranoproliferative glomerulonephritis has been proposed in the literature. The aim of this study was to compare the clinical, biochemical, etiology and renal biopsy findings of these patients grouped by immunofluorescence as proposed by the new classification. Methods: Patients with renal biopsy-proven membranoproliferative glomerulonephritis unrelated to systemic lupus erythematosus, diagnosed between 1999 and 2014. The patients were divided according to immunofluorescence: Immunoglobulin positive group, C3 positive only and negative immunofluorescence group. Results: We evaluated 92 patients, the majority of which were in the immunoglobulin positive group. Infectious diseases, hepatitis C virus and schistosomiasis, were the most frequent etiology. A negative immunofluorescence group had more vascular involvement in renal biopsy compare with others groups. Conclusions: The only difference between the groups was higher vascular involvement in renal biopsy in negative immunofluorescence group. These new classification was satisfactory for the finding of etiology in one part of the cases.
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spelling Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findingscomplement system proteinsepidemiologyglomerulonephritis, membranoproliferativemicroscopy, fluorescenceAbstract Background: New classification for membranoproliferative glomerulonephritis has been proposed in the literature. The aim of this study was to compare the clinical, biochemical, etiology and renal biopsy findings of these patients grouped by immunofluorescence as proposed by the new classification. Methods: Patients with renal biopsy-proven membranoproliferative glomerulonephritis unrelated to systemic lupus erythematosus, diagnosed between 1999 and 2014. The patients were divided according to immunofluorescence: Immunoglobulin positive group, C3 positive only and negative immunofluorescence group. Results: We evaluated 92 patients, the majority of which were in the immunoglobulin positive group. Infectious diseases, hepatitis C virus and schistosomiasis, were the most frequent etiology. A negative immunofluorescence group had more vascular involvement in renal biopsy compare with others groups. Conclusions: The only difference between the groups was higher vascular involvement in renal biopsy in negative immunofluorescence group. These new classification was satisfactory for the finding of etiology in one part of the cases.Sociedade Brasileira de Nefrologia2017-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000400447Brazilian Journal of Nephrology v.39 n.4 2017reponame:Jornal Brasileiro de Nefrologiainstname:Sociedade Brasileira de Nefrologia (SBN)instacron:SBN10.5935/0101-2800.20170078info:eu-repo/semantics/openAccessDias,Cristiane BitencourtTestagrossa,LeonardoJorge,LectíciaMalheiros,DeniseWoronik,Viktoriaeng2018-01-04T00:00:00Zoai:scielo:S0101-28002017000400447Revistahttp://www.bjn.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||jbn@sbn.org.br2175-82390101-2800opendoar:2018-01-04T00:00Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)false
dc.title.none.fl_str_mv Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
title Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
spellingShingle Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
Dias,Cristiane Bitencourt
complement system proteins
epidemiology
glomerulonephritis, membranoproliferative
microscopy, fluorescence
title_short Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
title_full Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
title_fullStr Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
title_full_unstemmed Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
title_sort Clinical and histological features of patients with membranoproliferative glomerulonephritis classified by immunofluorescence findings
author Dias,Cristiane Bitencourt
author_facet Dias,Cristiane Bitencourt
Testagrossa,Leonardo
Jorge,Lectícia
Malheiros,Denise
Woronik,Viktoria
author_role author
author2 Testagrossa,Leonardo
Jorge,Lectícia
Malheiros,Denise
Woronik,Viktoria
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Dias,Cristiane Bitencourt
Testagrossa,Leonardo
Jorge,Lectícia
Malheiros,Denise
Woronik,Viktoria
dc.subject.por.fl_str_mv complement system proteins
epidemiology
glomerulonephritis, membranoproliferative
microscopy, fluorescence
topic complement system proteins
epidemiology
glomerulonephritis, membranoproliferative
microscopy, fluorescence
description Abstract Background: New classification for membranoproliferative glomerulonephritis has been proposed in the literature. The aim of this study was to compare the clinical, biochemical, etiology and renal biopsy findings of these patients grouped by immunofluorescence as proposed by the new classification. Methods: Patients with renal biopsy-proven membranoproliferative glomerulonephritis unrelated to systemic lupus erythematosus, diagnosed between 1999 and 2014. The patients were divided according to immunofluorescence: Immunoglobulin positive group, C3 positive only and negative immunofluorescence group. Results: We evaluated 92 patients, the majority of which were in the immunoglobulin positive group. Infectious diseases, hepatitis C virus and schistosomiasis, were the most frequent etiology. A negative immunofluorescence group had more vascular involvement in renal biopsy compare with others groups. Conclusions: The only difference between the groups was higher vascular involvement in renal biopsy in negative immunofluorescence group. These new classification was satisfactory for the finding of etiology in one part of the cases.
publishDate 2017
dc.date.none.fl_str_mv 2017-12-01
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=S0101-28002017000400447
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002017000400447
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0101-2800.20170078
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 Nefrologia
publisher.none.fl_str_mv Sociedade Brasileira de Nefrologia
dc.source.none.fl_str_mv Brazilian Journal of Nephrology v.39 n.4 2017
reponame:Jornal Brasileiro de Nefrologia
instname:Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
instname_str Sociedade Brasileira de Nefrologia (SBN)
instacron_str SBN
institution SBN
reponame_str Jornal Brasileiro de Nefrologia
collection Jornal Brasileiro de Nefrologia
repository.name.fl_str_mv Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)
repository.mail.fl_str_mv ||jbn@sbn.org.br
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