Prognostic factors in adult patients with idiopathic IgA Nephropathy
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692012000200004 |
Resumo: | Introduction. IgA nephropathy is the dominant primary glomerular disease found throughout the majority of the worlds developed countries. Accurately identifying patients who are at risk of progressive disease is challenging. We aimed to characterise clinical and histological features that predict poor prognosis in adults. Patient and Methods. We performed a single-centre retrospective observational study of biopsy-proven IgA nephropathy. The primary outcome was renal survival and death from any cause, and the secondary outcome was proteinuria remission. Results.Data from 49 cases were available for analysis with a median follow-up of 4 years. There were no deaths. Univariableanalyses identified acute renal failure, low estimated glomerular filtration rate for ≥3 months (low eGFR), arterial hypertension, baseline proteinuria, glomerular sclerosis >50% and interstitial fibrosis >50% as poor prognostic markers. Low eGFR persisted significant by multivariable model that used only clinical parameters. Multivariable models with histopathologic parameters observed that tubular atrophy/interstitial fibrosis >50% was independently associated with the primary outcome. Proteinuria remission throughout follow-up had no prognostic value in our revision. Conclusions.Two independent predictors of poor renal survival at time of biopsy were found: low eGFR and tubular atrophy/interstitial fibrosis >50%. |
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7160 |
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Prognostic factors in adult patients with idiopathic IgA NephropathyIgAnephropathyprognostic factorsIntroduction. IgA nephropathy is the dominant primary glomerular disease found throughout the majority of the worlds developed countries. Accurately identifying patients who are at risk of progressive disease is challenging. We aimed to characterise clinical and histological features that predict poor prognosis in adults. Patient and Methods. We performed a single-centre retrospective observational study of biopsy-proven IgA nephropathy. The primary outcome was renal survival and death from any cause, and the secondary outcome was proteinuria remission. Results.Data from 49 cases were available for analysis with a median follow-up of 4 years. There were no deaths. Univariableanalyses identified acute renal failure, low estimated glomerular filtration rate for ≥3 months (low eGFR), arterial hypertension, baseline proteinuria, glomerular sclerosis >50% and interstitial fibrosis >50% as poor prognostic markers. Low eGFR persisted significant by multivariable model that used only clinical parameters. Multivariable models with histopathologic parameters observed that tubular atrophy/interstitial fibrosis >50% was independently associated with the primary outcome. Proteinuria remission throughout follow-up had no prognostic value in our revision. Conclusions.Two independent predictors of poor renal survival at time of biopsy were found: low eGFR and tubular atrophy/interstitial fibrosis >50%.Sociedade Portuguesa de Nefrologia2012-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692012000200004Portuguese Journal of Nephrology & Hypertension v.26 n.2 2012reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692012000200004Silva,CristinaAfonso,NunoCotovio,PatriciaMarques,MariaCarvalho,FernandaCarreira,Armandoinfo:eu-repo/semantics/openAccess2024-02-06T17:04:39Zoai:scielo:S0872-01692012000200004Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:18:48.922095Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Prognostic factors in adult patients with idiopathic IgA Nephropathy |
title |
Prognostic factors in adult patients with idiopathic IgA Nephropathy |
spellingShingle |
Prognostic factors in adult patients with idiopathic IgA Nephropathy Silva,Cristina IgAnephropathy prognostic factors |
title_short |
Prognostic factors in adult patients with idiopathic IgA Nephropathy |
title_full |
Prognostic factors in adult patients with idiopathic IgA Nephropathy |
title_fullStr |
Prognostic factors in adult patients with idiopathic IgA Nephropathy |
title_full_unstemmed |
Prognostic factors in adult patients with idiopathic IgA Nephropathy |
title_sort |
Prognostic factors in adult patients with idiopathic IgA Nephropathy |
author |
Silva,Cristina |
author_facet |
Silva,Cristina Afonso,Nuno Cotovio,Patricia Marques,Maria Carvalho,Fernanda Carreira,Armando |
author_role |
author |
author2 |
Afonso,Nuno Cotovio,Patricia Marques,Maria Carvalho,Fernanda Carreira,Armando |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Silva,Cristina Afonso,Nuno Cotovio,Patricia Marques,Maria Carvalho,Fernanda Carreira,Armando |
dc.subject.por.fl_str_mv |
IgAnephropathy prognostic factors |
topic |
IgAnephropathy prognostic factors |
description |
Introduction. IgA nephropathy is the dominant primary glomerular disease found throughout the majority of the worlds developed countries. Accurately identifying patients who are at risk of progressive disease is challenging. We aimed to characterise clinical and histological features that predict poor prognosis in adults. Patient and Methods. We performed a single-centre retrospective observational study of biopsy-proven IgA nephropathy. The primary outcome was renal survival and death from any cause, and the secondary outcome was proteinuria remission. Results.Data from 49 cases were available for analysis with a median follow-up of 4 years. There were no deaths. Univariableanalyses identified acute renal failure, low estimated glomerular filtration rate for ≥3 months (low eGFR), arterial hypertension, baseline proteinuria, glomerular sclerosis >50% and interstitial fibrosis >50% as poor prognostic markers. Low eGFR persisted significant by multivariable model that used only clinical parameters. Multivariable models with histopathologic parameters observed that tubular atrophy/interstitial fibrosis >50% was independently associated with the primary outcome. Proteinuria remission throughout follow-up had no prognostic value in our revision. Conclusions.Two independent predictors of poor renal survival at time of biopsy were found: low eGFR and tubular atrophy/interstitial fibrosis >50%. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-04-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692012000200004 |
url |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692012000200004 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692012000200004 |
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 Portuguesa de Nefrologia |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Nefrologia |
dc.source.none.fl_str_mv |
Portuguese Journal of Nephrology & Hypertension v.26 n.2 2012 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799137278314938368 |