Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?

Detalhes bibliográficos
Autor(a) principal: Nasri,Hamid
Data de Publicação: 2014
Outros Autores: Mubarak,Muhammed
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=S0872-01692014000300004
Resumo: Background: The lesions resembling focal segmental glomerulosclerosis (FSGS) are frequently found concurrently with IgA nephropathy (IgAN). However, there is controversy regarding the significance of this co -existence. In this study, we sought to determine the significance of FSGS-like lesions in a group of IgAN patients, especially with regard to the Oxford classification. Patients and Methods: The FSGS lesions were typed according to the Columbia classification and correlated with clinico -pathological parameters including Oxford classification criteria. Individual lesions suggesting FSGS were also evaluated. IgAN lesions were classified according to the Oxford classification. Results: Of 114 patients, 80 (70.2 %) were male. The mean age of patients was 37.7 ± 13.6 years. Of 35 patients with co-existent IgAN and FSGS, 50% had classic variant (not otherwise specified; NOS), 30% had tip and 20% perihilar variant of FSGS. None of the patients had collapsing or cellular variants. A significantly positive association of FSGS with M (p = 0.001), S (p = 0.001) and T p = 0.001) variables of Oxford classification was found. No significant difference of FSGS, hyalinosis, capsular adhesions and podocytopathy was found between males and females (p > 0.05). However, a significantly positive association of proteinuria (p = 0.037) and renal dysfunction (p = 0.026) with podocytopathy, and of serum creatinine and renal dysfunction with the presence of FSGS (p = 0.027, p = 0.001, respectively) was seen. Conclusion: In conclusion, the concurrence of FSGS -like lesions with IgAN is associated with the established poor clinical and pathological prognostic factors of this disease and the lesions appear to be of prognostic significance. The presence of such lesions should be sought diligently on renal biopsy examination.
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spelling Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?Columbia classification focal segmental glomerulosclerosisIgA nephropathyOxford classificationproteinuriarenal failureBackground: The lesions resembling focal segmental glomerulosclerosis (FSGS) are frequently found concurrently with IgA nephropathy (IgAN). However, there is controversy regarding the significance of this co -existence. In this study, we sought to determine the significance of FSGS-like lesions in a group of IgAN patients, especially with regard to the Oxford classification. Patients and Methods: The FSGS lesions were typed according to the Columbia classification and correlated with clinico -pathological parameters including Oxford classification criteria. Individual lesions suggesting FSGS were also evaluated. IgAN lesions were classified according to the Oxford classification. Results: Of 114 patients, 80 (70.2 %) were male. The mean age of patients was 37.7 ± 13.6 years. Of 35 patients with co-existent IgAN and FSGS, 50% had classic variant (not otherwise specified; NOS), 30% had tip and 20% perihilar variant of FSGS. None of the patients had collapsing or cellular variants. A significantly positive association of FSGS with M (p = 0.001), S (p = 0.001) and T p = 0.001) variables of Oxford classification was found. No significant difference of FSGS, hyalinosis, capsular adhesions and podocytopathy was found between males and females (p > 0.05). However, a significantly positive association of proteinuria (p = 0.037) and renal dysfunction (p = 0.026) with podocytopathy, and of serum creatinine and renal dysfunction with the presence of FSGS (p = 0.027, p = 0.001, respectively) was seen. Conclusion: In conclusion, the concurrence of FSGS -like lesions with IgAN is associated with the established poor clinical and pathological prognostic factors of this disease and the lesions appear to be of prognostic significance. The presence of such lesions should be sought diligently on renal biopsy examination.Sociedade Portuguesa de Nefrologia2014-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692014000300004Portuguese Journal of Nephrology & 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=S0872-01692014000300004Nasri,HamidMubarak,Muhammedinfo:eu-repo/semantics/openAccess2024-02-06T17:04:45Zoai:scielo:S0872-01692014000300004Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:18:52.848640Repositório 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 Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
title Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
spellingShingle Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
Nasri,Hamid
Columbia classification focal segmental glomerulosclerosis
IgA nephropathy
Oxford classification
proteinuria
renal failure
title_short Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
title_full Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
title_fullStr Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
title_full_unstemmed Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
title_sort Focal segmental glomerulosclerosis in IgA nephropathy with regard to Oxford classification: Does it matter?
author Nasri,Hamid
author_facet Nasri,Hamid
Mubarak,Muhammed
author_role author
author2 Mubarak,Muhammed
author2_role author
dc.contributor.author.fl_str_mv Nasri,Hamid
Mubarak,Muhammed
dc.subject.por.fl_str_mv Columbia classification focal segmental glomerulosclerosis
IgA nephropathy
Oxford classification
proteinuria
renal failure
topic Columbia classification focal segmental glomerulosclerosis
IgA nephropathy
Oxford classification
proteinuria
renal failure
description Background: The lesions resembling focal segmental glomerulosclerosis (FSGS) are frequently found concurrently with IgA nephropathy (IgAN). However, there is controversy regarding the significance of this co -existence. In this study, we sought to determine the significance of FSGS-like lesions in a group of IgAN patients, especially with regard to the Oxford classification. Patients and Methods: The FSGS lesions were typed according to the Columbia classification and correlated with clinico -pathological parameters including Oxford classification criteria. Individual lesions suggesting FSGS were also evaluated. IgAN lesions were classified according to the Oxford classification. Results: Of 114 patients, 80 (70.2 %) were male. The mean age of patients was 37.7 ± 13.6 years. Of 35 patients with co-existent IgAN and FSGS, 50% had classic variant (not otherwise specified; NOS), 30% had tip and 20% perihilar variant of FSGS. None of the patients had collapsing or cellular variants. A significantly positive association of FSGS with M (p = 0.001), S (p = 0.001) and T p = 0.001) variables of Oxford classification was found. No significant difference of FSGS, hyalinosis, capsular adhesions and podocytopathy was found between males and females (p > 0.05). However, a significantly positive association of proteinuria (p = 0.037) and renal dysfunction (p = 0.026) with podocytopathy, and of serum creatinine and renal dysfunction with the presence of FSGS (p = 0.027, p = 0.001, respectively) was seen. Conclusion: In conclusion, the concurrence of FSGS -like lesions with IgAN is associated with the established poor clinical and pathological prognostic factors of this disease and the lesions appear to be of prognostic significance. The presence of such lesions should be sought diligently on renal biopsy examination.
publishDate 2014
dc.date.none.fl_str_mv 2014-09-01
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dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692014000300004
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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.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
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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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