Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy

Detalhes bibliográficos
Autor(a) principal: Neves,Marta
Data de Publicação: 2014
Outros Autores: Rodrigues,Luis, Sa,Helena, Pratas,Jorge, Campos,Maria
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=S0872-01692014000300006
Resumo: Background: Some clinical and laboratory features may provide clues to the diagnosis of specific glomerular diseases. However, the kidney biopsy remains the gold standard in the diagnosis of parenchymal disease. Aim: To compare presenting clinical and laboratory features and report outcomes of adult patients with proteinuria diagnosed with primary minimal change disease (MCD), focal and segmental glomerulosclerosis (FSGS), and membranous nephropathy (MN). Subjects and Methods: Retrospective study of 143 patients over the age of eighteen years diagnosed with primary MCD, FSGS or MN, between 1981 and 2009. The groups were compared regarding presenting features and outcomes. Results: The most common glomerulopathy was MN (49.7%), followed by MCD (25.2%) and FSGS (25.2%). Statistically significant differences (p < 0.05) were found between the three groups regarding proteinuria, serum albumin, total cholesterol and serum creatinine higher than 1.5 mg/dl at the time of kidney biopsy, as well as the motive for the biopsy. No statistical differences were found between the three histological groups regarding remission at the end of the follow-up. Statistically significant differences (p < 0.05) were determined between the three groups regarding time to partial and complete remission, proteinuria and serum albumin at the final evaluation, and infectious complications. Conclusions: Patients with MCD presented lower serum albumin and higher levels of 24 -hour proteinuria and total cholesterol than the other groups. Patients with MCD achieved remission sooner, but suffered more infectious complications than those with FSGS or MN. In turn, patients with FSGS had higher proteinuria at the final evaluation and a trend towards the need for long-term RRT.
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spelling Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathyFocal and segmental glomerulosclerosismembranous nephropathyminimal change diseaseproteinuriaBackground: Some clinical and laboratory features may provide clues to the diagnosis of specific glomerular diseases. However, the kidney biopsy remains the gold standard in the diagnosis of parenchymal disease. Aim: To compare presenting clinical and laboratory features and report outcomes of adult patients with proteinuria diagnosed with primary minimal change disease (MCD), focal and segmental glomerulosclerosis (FSGS), and membranous nephropathy (MN). Subjects and Methods: Retrospective study of 143 patients over the age of eighteen years diagnosed with primary MCD, FSGS or MN, between 1981 and 2009. The groups were compared regarding presenting features and outcomes. Results: The most common glomerulopathy was MN (49.7%), followed by MCD (25.2%) and FSGS (25.2%). Statistically significant differences (p < 0.05) were found between the three groups regarding proteinuria, serum albumin, total cholesterol and serum creatinine higher than 1.5 mg/dl at the time of kidney biopsy, as well as the motive for the biopsy. No statistical differences were found between the three histological groups regarding remission at the end of the follow-up. Statistically significant differences (p < 0.05) were determined between the three groups regarding time to partial and complete remission, proteinuria and serum albumin at the final evaluation, and infectious complications. Conclusions: Patients with MCD presented lower serum albumin and higher levels of 24 -hour proteinuria and total cholesterol than the other groups. Patients with MCD achieved remission sooner, but suffered more infectious complications than those with FSGS or MN. In turn, patients with FSGS had higher proteinuria at the final evaluation and a trend towards the need for long-term RRT.Sociedade Portuguesa de Nefrologia2014-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692014000300006Portuguese Journal of Nephrology &amp; Hypertension v.28 n.3 2014reponame: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=S0872-01692014000300006Neves,MartaRodrigues,LuisSa,HelenaPratas,JorgeCampos,Mariainfo:eu-repo/semantics/openAccess2024-02-06T17:04:46Zoai:scielo:S0872-01692014000300006Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:18:52.941825Repositório 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 Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
title Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
spellingShingle Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
Neves,Marta
Focal and segmental glomerulosclerosis
membranous nephropathy
minimal change disease
proteinuria
title_short Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
title_full Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
title_fullStr Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
title_full_unstemmed Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
title_sort Clinicopathological correlations in proteinuric diseases: presenting features of patients with minimal change disease, focal and segmental glomerulosclerosis and membranous nephropathy
author Neves,Marta
author_facet Neves,Marta
Rodrigues,Luis
Sa,Helena
Pratas,Jorge
Campos,Maria
author_role author
author2 Rodrigues,Luis
Sa,Helena
Pratas,Jorge
Campos,Maria
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Neves,Marta
Rodrigues,Luis
Sa,Helena
Pratas,Jorge
Campos,Maria
dc.subject.por.fl_str_mv Focal and segmental glomerulosclerosis
membranous nephropathy
minimal change disease
proteinuria
topic Focal and segmental glomerulosclerosis
membranous nephropathy
minimal change disease
proteinuria
description Background: Some clinical and laboratory features may provide clues to the diagnosis of specific glomerular diseases. However, the kidney biopsy remains the gold standard in the diagnosis of parenchymal disease. Aim: To compare presenting clinical and laboratory features and report outcomes of adult patients with proteinuria diagnosed with primary minimal change disease (MCD), focal and segmental glomerulosclerosis (FSGS), and membranous nephropathy (MN). Subjects and Methods: Retrospective study of 143 patients over the age of eighteen years diagnosed with primary MCD, FSGS or MN, between 1981 and 2009. The groups were compared regarding presenting features and outcomes. Results: The most common glomerulopathy was MN (49.7%), followed by MCD (25.2%) and FSGS (25.2%). Statistically significant differences (p < 0.05) were found between the three groups regarding proteinuria, serum albumin, total cholesterol and serum creatinine higher than 1.5 mg/dl at the time of kidney biopsy, as well as the motive for the biopsy. No statistical differences were found between the three histological groups regarding remission at the end of the follow-up. Statistically significant differences (p < 0.05) were determined between the three groups regarding time to partial and complete remission, proteinuria and serum albumin at the final evaluation, and infectious complications. Conclusions: Patients with MCD presented lower serum albumin and higher levels of 24 -hour proteinuria and total cholesterol than the other groups. Patients with MCD achieved remission sooner, but suffered more infectious complications than those with FSGS or MN. In turn, patients with FSGS had higher proteinuria at the final evaluation and a trend towards the need for long-term RRT.
publishDate 2014
dc.date.none.fl_str_mv 2014-09-01
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format article
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dc.language.iso.fl_str_mv eng
language eng
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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 &amp; Hypertension v.28 n.3 2014
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str 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
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