Prognostic factors in adult patients with idiopathic IgA Nephropathy

Detalhes bibliográficos
Autor(a) principal: Silva,Cristina
Data de Publicação: 2012
Outros Autores: Afonso,Nuno, Cotovio,Patricia, Marques,Maria, Carvalho,Fernanda, Carreira,Armando
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 world’s 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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spelling Prognostic factors in adult patients with idiopathic IgA NephropathyIgAnephropathyprognostic factorsIntroduction. IgA nephropathy is the dominant primary glomerular disease found throughout the majority of the world’s 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 world’s 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
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dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692012000200004
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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
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