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Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease

INTRODUCTION: Minimal change disease is a common cause of nephrotic syndrome. In general, patients with minimal change disease respond to corticosteroids and have excellent long-term renal survival. However, some patients have less favorable outcome. These patients are often thought to have progress...

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Autores principales: van de Lest, Nina A., Zandbergen, Malu, IJpelaar, Daphne H.T., Wolterbeek, Ron, Bruijn, Jan A., Bajema, Ingeborg M., Scharpfenecker, Marion
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762955/
https://www.ncbi.nlm.nih.gov/pubmed/29340328
http://dx.doi.org/10.1016/j.ekir.2017.09.011
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author van de Lest, Nina A.
Zandbergen, Malu
IJpelaar, Daphne H.T.
Wolterbeek, Ron
Bruijn, Jan A.
Bajema, Ingeborg M.
Scharpfenecker, Marion
author_facet van de Lest, Nina A.
Zandbergen, Malu
IJpelaar, Daphne H.T.
Wolterbeek, Ron
Bruijn, Jan A.
Bajema, Ingeborg M.
Scharpfenecker, Marion
author_sort van de Lest, Nina A.
collection PubMed
description INTRODUCTION: Minimal change disease is a common cause of nephrotic syndrome. In general, patients with minimal change disease respond to corticosteroids and have excellent long-term renal survival. However, some patients have less favorable outcome. These patients are often thought to have progressed to focal segmental glomerulosclerosis. We previously reported that a segmental loss of podocyte markers is present before the development of focal segmental glomerulosclerosis in a rat model. Here, we investigated whether loss of podocyte marker nephrin can serve as a biomarker for predicting poor outcome in patients with minimal change disease. METHODS: We obtained 47 kidney biopsy samples from patients diagnosed with minimal change disease and stained sections with periodic acid−Schiff and for nephrin. Nephrin loss was scored by 2 independent researchers who were blinded to clinical outcome. Clinical data were collected retrospectively, and nephrin loss was correlated with clinical follow-up data. RESULTS: Nephrin loss was present in 34% of the biopsy samples. During follow-up, patients with nephrin loss achieved remission less frequently (61%) compared to patients without (96%) (P = 0.002). Moreover, 5-year eGFR was lower in the patients with renal nephrin loss. The risk of eGFR decreasing to < 60 ml/min per 1.73m(2) increased with each percentage of glomeruli with nephrin loss (hazard ratio = 1.044, 95% confidence interval = 1.02−1.07). CONCLUSION: These results indicate that nephrin loss in patients with minimal change disease can help predict both remission and long-term renal outcome.
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spelling pubmed-57629552018-01-16 Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease van de Lest, Nina A. Zandbergen, Malu IJpelaar, Daphne H.T. Wolterbeek, Ron Bruijn, Jan A. Bajema, Ingeborg M. Scharpfenecker, Marion Kidney Int Rep Clinical Research INTRODUCTION: Minimal change disease is a common cause of nephrotic syndrome. In general, patients with minimal change disease respond to corticosteroids and have excellent long-term renal survival. However, some patients have less favorable outcome. These patients are often thought to have progressed to focal segmental glomerulosclerosis. We previously reported that a segmental loss of podocyte markers is present before the development of focal segmental glomerulosclerosis in a rat model. Here, we investigated whether loss of podocyte marker nephrin can serve as a biomarker for predicting poor outcome in patients with minimal change disease. METHODS: We obtained 47 kidney biopsy samples from patients diagnosed with minimal change disease and stained sections with periodic acid−Schiff and for nephrin. Nephrin loss was scored by 2 independent researchers who were blinded to clinical outcome. Clinical data were collected retrospectively, and nephrin loss was correlated with clinical follow-up data. RESULTS: Nephrin loss was present in 34% of the biopsy samples. During follow-up, patients with nephrin loss achieved remission less frequently (61%) compared to patients without (96%) (P = 0.002). Moreover, 5-year eGFR was lower in the patients with renal nephrin loss. The risk of eGFR decreasing to < 60 ml/min per 1.73m(2) increased with each percentage of glomeruli with nephrin loss (hazard ratio = 1.044, 95% confidence interval = 1.02−1.07). CONCLUSION: These results indicate that nephrin loss in patients with minimal change disease can help predict both remission and long-term renal outcome. Elsevier 2017-09-28 /pmc/articles/PMC5762955/ /pubmed/29340328 http://dx.doi.org/10.1016/j.ekir.2017.09.011 Text en © 2017 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research
van de Lest, Nina A.
Zandbergen, Malu
IJpelaar, Daphne H.T.
Wolterbeek, Ron
Bruijn, Jan A.
Bajema, Ingeborg M.
Scharpfenecker, Marion
Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease
title Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease
title_full Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease
title_fullStr Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease
title_full_unstemmed Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease
title_short Nephrin Loss Can Be Used to Predict Remission and Long-term Renal Outcome in Patients With Minimal Change Disease
title_sort nephrin loss can be used to predict remission and long-term renal outcome in patients with minimal change disease
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762955/
https://www.ncbi.nlm.nih.gov/pubmed/29340328
http://dx.doi.org/10.1016/j.ekir.2017.09.011
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