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Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations
Denys–Drash syndrome (DDS) is characterized by progressive glomerulopathy caused by diffuse mesangial sclerosis (DMS), genitourinary defects, and a higher risk of developing Wilms’ tumor. It is commonly assumed that the DMS is unresponsive to any medications. In this report, we present a patient wit...
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068521/ https://www.ncbi.nlm.nih.gov/pubmed/20848129 http://dx.doi.org/10.1007/s00431-010-1278-4 |
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author | Wasilewska, Anna Maria Kuroczycka-Saniutycz, Elżbieta Zoch-Zwierz, Walentyna |
author_facet | Wasilewska, Anna Maria Kuroczycka-Saniutycz, Elżbieta Zoch-Zwierz, Walentyna |
author_sort | Wasilewska, Anna Maria |
collection | PubMed |
description | Denys–Drash syndrome (DDS) is characterized by progressive glomerulopathy caused by diffuse mesangial sclerosis (DMS), genitourinary defects, and a higher risk of developing Wilms’ tumor. It is commonly assumed that the DMS is unresponsive to any medications. In this report, we present a patient with Denys–Drash syndrome, in whom the cyclosporine A (CsA) was found to induce total remission. This observation and observations of other authors confirm that in genetic forms of nephrotic syndrome, the proteinuric effect of CsA may be due to a non-immunologic mechanism. We confirm the beneficial effect of CsA treatment in DDS; however, the potential nephrotoxicity of this drug will probably not allow long-term use. |
format | Text |
id | pubmed-3068521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-30685212011-04-05 Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations Wasilewska, Anna Maria Kuroczycka-Saniutycz, Elżbieta Zoch-Zwierz, Walentyna Eur J Pediatr Short Report Denys–Drash syndrome (DDS) is characterized by progressive glomerulopathy caused by diffuse mesangial sclerosis (DMS), genitourinary defects, and a higher risk of developing Wilms’ tumor. It is commonly assumed that the DMS is unresponsive to any medications. In this report, we present a patient with Denys–Drash syndrome, in whom the cyclosporine A (CsA) was found to induce total remission. This observation and observations of other authors confirm that in genetic forms of nephrotic syndrome, the proteinuric effect of CsA may be due to a non-immunologic mechanism. We confirm the beneficial effect of CsA treatment in DDS; however, the potential nephrotoxicity of this drug will probably not allow long-term use. Springer-Verlag 2010-09-17 2011 /pmc/articles/PMC3068521/ /pubmed/20848129 http://dx.doi.org/10.1007/s00431-010-1278-4 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Short Report Wasilewska, Anna Maria Kuroczycka-Saniutycz, Elżbieta Zoch-Zwierz, Walentyna Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations |
title | Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations |
title_full | Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations |
title_fullStr | Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations |
title_full_unstemmed | Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations |
title_short | Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations |
title_sort | effect of cyclosporin a on proteinuria in the course of glomerulopathy associated with wt1 mutations |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068521/ https://www.ncbi.nlm.nih.gov/pubmed/20848129 http://dx.doi.org/10.1007/s00431-010-1278-4 |
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