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Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy

BACKGROUND: Proteinuria is the most important risk factor for IgA nephropathy progression. The purpose of this study is to evaluate the long-term outcome and risk factors for poor prognosis in childhood IgA nephropathy. METHODS: Patients who were diagnosed with IgA nephropathy between 1972 and 1992...

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Autores principales: Kamei, Koichi, Harada, Ryoko, Hamada, Riku, Sakai, Tomoyuki, Hamasaki, Yuko, Hataya, Hiroshi, Ito, Shuichi, Ishikura, Kenji, Honda, Masataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792393/
https://www.ncbi.nlm.nih.gov/pubmed/26978656
http://dx.doi.org/10.1371/journal.pone.0150885
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author Kamei, Koichi
Harada, Ryoko
Hamada, Riku
Sakai, Tomoyuki
Hamasaki, Yuko
Hataya, Hiroshi
Ito, Shuichi
Ishikura, Kenji
Honda, Masataka
author_facet Kamei, Koichi
Harada, Ryoko
Hamada, Riku
Sakai, Tomoyuki
Hamasaki, Yuko
Hataya, Hiroshi
Ito, Shuichi
Ishikura, Kenji
Honda, Masataka
author_sort Kamei, Koichi
collection PubMed
description BACKGROUND: Proteinuria is the most important risk factor for IgA nephropathy progression. The purpose of this study is to evaluate the long-term outcome and risk factors for poor prognosis in childhood IgA nephropathy. METHODS: Patients who were diagnosed with IgA nephropathy between 1972 and 1992 at the Tokyo Metropolitan Kiyose Children’s Hospital were included. We analyzed risk factors for progression to end-stage kidney disease (ESKD) and chronic renal insufficiency (CRI) using Kaplan-Meier method and multivariate analyses of Cox proportional hazard model. RESULTS: One hundred patients were included and the median observation period was 11.8 years. Twelve and 17 patients progressed to ESKD and CRI, respectively. The survival probabilities were 90.0% at 10 years and 79.8% at 20 years for ESKD, and 86.1% at 10 years and 72.3% at 20 years for CRI. Notably, patients with heavy proteinuria with hypoalbuminemia during follow-up period showed extremely poor prognosis. In this group, the survival rate at 10 years from ESKD and CRI was 40.6% and 20.8%, respectively. By multivariate analysis, proteinuria at diagnosis and proteinuria during follow-up period were risk factors for ESKD, whereas glomeruli showing mesangial proliferation ≥50% and proteinuria during follow-up period were risk factors for CRI. Patients without heavy proteinuria during follow-up period did not develop CRI and 63% of patients with mild proteinuria during follow-up period showed no proteinuria at the last observation. CONCLUSIONS: The degree of proteinuria during follow-up period is the strongest risk factor for ESKD and CRI.
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spelling pubmed-47923932016-03-23 Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy Kamei, Koichi Harada, Ryoko Hamada, Riku Sakai, Tomoyuki Hamasaki, Yuko Hataya, Hiroshi Ito, Shuichi Ishikura, Kenji Honda, Masataka PLoS One Research Article BACKGROUND: Proteinuria is the most important risk factor for IgA nephropathy progression. The purpose of this study is to evaluate the long-term outcome and risk factors for poor prognosis in childhood IgA nephropathy. METHODS: Patients who were diagnosed with IgA nephropathy between 1972 and 1992 at the Tokyo Metropolitan Kiyose Children’s Hospital were included. We analyzed risk factors for progression to end-stage kidney disease (ESKD) and chronic renal insufficiency (CRI) using Kaplan-Meier method and multivariate analyses of Cox proportional hazard model. RESULTS: One hundred patients were included and the median observation period was 11.8 years. Twelve and 17 patients progressed to ESKD and CRI, respectively. The survival probabilities were 90.0% at 10 years and 79.8% at 20 years for ESKD, and 86.1% at 10 years and 72.3% at 20 years for CRI. Notably, patients with heavy proteinuria with hypoalbuminemia during follow-up period showed extremely poor prognosis. In this group, the survival rate at 10 years from ESKD and CRI was 40.6% and 20.8%, respectively. By multivariate analysis, proteinuria at diagnosis and proteinuria during follow-up period were risk factors for ESKD, whereas glomeruli showing mesangial proliferation ≥50% and proteinuria during follow-up period were risk factors for CRI. Patients without heavy proteinuria during follow-up period did not develop CRI and 63% of patients with mild proteinuria during follow-up period showed no proteinuria at the last observation. CONCLUSIONS: The degree of proteinuria during follow-up period is the strongest risk factor for ESKD and CRI. Public Library of Science 2016-03-15 /pmc/articles/PMC4792393/ /pubmed/26978656 http://dx.doi.org/10.1371/journal.pone.0150885 Text en © 2016 Kamei et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kamei, Koichi
Harada, Ryoko
Hamada, Riku
Sakai, Tomoyuki
Hamasaki, Yuko
Hataya, Hiroshi
Ito, Shuichi
Ishikura, Kenji
Honda, Masataka
Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy
title Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy
title_full Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy
title_fullStr Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy
title_full_unstemmed Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy
title_short Proteinuria during Follow-Up Period and Long-Term Renal Survival of Childhood IgA Nephropathy
title_sort proteinuria during follow-up period and long-term renal survival of childhood iga nephropathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792393/
https://www.ncbi.nlm.nih.gov/pubmed/26978656
http://dx.doi.org/10.1371/journal.pone.0150885
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