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Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children
BACKGROUND: Nephrotic syndrome (NS) is the term used for the association of edema and massive proteinuria. From a therapeutic point of view, it is important to distinguish between primitive and secondary kidney damage. The clinical evolution, prognosis and therapeutic response in the NS in children...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034867/ https://www.ncbi.nlm.nih.gov/pubmed/35469261 http://dx.doi.org/10.2147/IJGM.S348346 |
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author | Starcea, Iuliana Magdalena Bogos, Roxana Alexandra Scurtu, Georgiana Munteanu, Mihaela Russu, Radu Lupu, Vasile Valeriu Lupu, Ancuta Trandafir, Laura Miron, Ingrith Crenguta Mocanu, Maria Adriana |
author_facet | Starcea, Iuliana Magdalena Bogos, Roxana Alexandra Scurtu, Georgiana Munteanu, Mihaela Russu, Radu Lupu, Vasile Valeriu Lupu, Ancuta Trandafir, Laura Miron, Ingrith Crenguta Mocanu, Maria Adriana |
author_sort | Starcea, Iuliana Magdalena |
collection | PubMed |
description | BACKGROUND: Nephrotic syndrome (NS) is the term used for the association of edema and massive proteinuria. From a therapeutic point of view, it is important to distinguish between primitive and secondary kidney damage. The clinical evolution, prognosis and therapeutic response in the NS in children are directly determined by the anatomopathological aspect. Steroid resistant nephrotic syndrome was diagnosed in patients with idiopathic NS based on lack of complete remission despite treatment with steroids. PURPOSE: To analyse the anatomopathological aspects of steroid resistant nephrotic syndrome (SRNS) and their correlation with evolution. MATERIALS AND METHODS: We made a retrospective study with the aim to analyze the anatomo-pathological aspects and their correlations with evolution in 68 cases of steroid resistant nephrotic syndrome (SRNS) hospitalized in the Pediatric Nephrology Department in Iaşi, Romania. We defined SRNS in all cases without response to corticosteroids after the first month of therapy. For all the cases selected, the period of follow-up was the minimal 6 months. RESULTS AND DISCUSSIONS: A 36% case of nephrotic syndrome was corticoresistant, with the mean age at onset of patients with SRNS being 9.18 years, compared to KDIGO studies in which the corticosteroid resistance is 10–20%. Renal biopsy was performed in 80.88% children with SRNS and was allowed the evaluation of the activity and chronicity index. Total remission was obtained in 44.01% children with SRNS. The correlation of the anatomopathological aspects with the evolution is not statistically significant (p = 0.76), observing different therapeutic responses to all the analyzed histological types. CONCLUSION: Almost half of NS in children are cortico resistant. Remission was obtained in 44% of cases of SRNS. Predicting the response to long-term treatment in SRNS is difficult using only renal biopsy; it is necessary to introduce genetic molecular analyses to establish a judicious therapeutic attitude. |
format | Online Article Text |
id | pubmed-9034867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-90348672022-04-24 Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children Starcea, Iuliana Magdalena Bogos, Roxana Alexandra Scurtu, Georgiana Munteanu, Mihaela Russu, Radu Lupu, Vasile Valeriu Lupu, Ancuta Trandafir, Laura Miron, Ingrith Crenguta Mocanu, Maria Adriana Int J Gen Med Original Research BACKGROUND: Nephrotic syndrome (NS) is the term used for the association of edema and massive proteinuria. From a therapeutic point of view, it is important to distinguish between primitive and secondary kidney damage. The clinical evolution, prognosis and therapeutic response in the NS in children are directly determined by the anatomopathological aspect. Steroid resistant nephrotic syndrome was diagnosed in patients with idiopathic NS based on lack of complete remission despite treatment with steroids. PURPOSE: To analyse the anatomopathological aspects of steroid resistant nephrotic syndrome (SRNS) and their correlation with evolution. MATERIALS AND METHODS: We made a retrospective study with the aim to analyze the anatomo-pathological aspects and their correlations with evolution in 68 cases of steroid resistant nephrotic syndrome (SRNS) hospitalized in the Pediatric Nephrology Department in Iaşi, Romania. We defined SRNS in all cases without response to corticosteroids after the first month of therapy. For all the cases selected, the period of follow-up was the minimal 6 months. RESULTS AND DISCUSSIONS: A 36% case of nephrotic syndrome was corticoresistant, with the mean age at onset of patients with SRNS being 9.18 years, compared to KDIGO studies in which the corticosteroid resistance is 10–20%. Renal biopsy was performed in 80.88% children with SRNS and was allowed the evaluation of the activity and chronicity index. Total remission was obtained in 44.01% children with SRNS. The correlation of the anatomopathological aspects with the evolution is not statistically significant (p = 0.76), observing different therapeutic responses to all the analyzed histological types. CONCLUSION: Almost half of NS in children are cortico resistant. Remission was obtained in 44% of cases of SRNS. Predicting the response to long-term treatment in SRNS is difficult using only renal biopsy; it is necessary to introduce genetic molecular analyses to establish a judicious therapeutic attitude. Dove 2022-04-19 /pmc/articles/PMC9034867/ /pubmed/35469261 http://dx.doi.org/10.2147/IJGM.S348346 Text en © 2022 Starcea et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Starcea, Iuliana Magdalena Bogos, Roxana Alexandra Scurtu, Georgiana Munteanu, Mihaela Russu, Radu Lupu, Vasile Valeriu Lupu, Ancuta Trandafir, Laura Miron, Ingrith Crenguta Mocanu, Maria Adriana Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children |
title | Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children |
title_full | Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children |
title_fullStr | Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children |
title_full_unstemmed | Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children |
title_short | Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children |
title_sort | pathological and evolutive correlations in steroid resistant nephrotic syndrome in children |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034867/ https://www.ncbi.nlm.nih.gov/pubmed/35469261 http://dx.doi.org/10.2147/IJGM.S348346 |
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