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Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children

Focal segmental glomerulosclerosis (FSGS) is a nephrotic syndrome. Up to around 80% of cases of primary FSGS are resistant to steroid treatment. A large proportion of patients with steroid-resistant FSGS progress to end-stage renal disease. The purpose of treatment is to obtain a complete remission...

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Autores principales: Han, Kyoung Hee, Kim, Seong Heon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852325/
https://www.ncbi.nlm.nih.gov/pubmed/27195285
http://dx.doi.org/10.1155/2016/3053706
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author Han, Kyoung Hee
Kim, Seong Heon
author_facet Han, Kyoung Hee
Kim, Seong Heon
author_sort Han, Kyoung Hee
collection PubMed
description Focal segmental glomerulosclerosis (FSGS) is a nephrotic syndrome. Up to around 80% of cases of primary FSGS are resistant to steroid treatment. A large proportion of patients with steroid-resistant FSGS progress to end-stage renal disease. The purpose of treatment is to obtain a complete remission of proteinuria, a necessary step that precedes improved renal survival and reduces the risk of progression to chronic kidney disease. When this is not possible, the secondary goal is a partial remission of proteinuria. Reduction or remission of proteinuria is the most important factor predictive of renal survival. We will review the current updated strategies for treatment of primary FSGS in children, including traditional therapies consisting of corticosteroids and calcineurin inhibitors and novel therapies such as rituximab, abatacept, adalimumab, and fresolimumab.
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spelling pubmed-48523252016-05-18 Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children Han, Kyoung Hee Kim, Seong Heon Biomed Res Int Review Article Focal segmental glomerulosclerosis (FSGS) is a nephrotic syndrome. Up to around 80% of cases of primary FSGS are resistant to steroid treatment. A large proportion of patients with steroid-resistant FSGS progress to end-stage renal disease. The purpose of treatment is to obtain a complete remission of proteinuria, a necessary step that precedes improved renal survival and reduces the risk of progression to chronic kidney disease. When this is not possible, the secondary goal is a partial remission of proteinuria. Reduction or remission of proteinuria is the most important factor predictive of renal survival. We will review the current updated strategies for treatment of primary FSGS in children, including traditional therapies consisting of corticosteroids and calcineurin inhibitors and novel therapies such as rituximab, abatacept, adalimumab, and fresolimumab. Hindawi Publishing Corporation 2016 2016-04-18 /pmc/articles/PMC4852325/ /pubmed/27195285 http://dx.doi.org/10.1155/2016/3053706 Text en Copyright © 2016 K. H. Han and S. H. Kim. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Han, Kyoung Hee
Kim, Seong Heon
Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children
title Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children
title_full Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children
title_fullStr Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children
title_full_unstemmed Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children
title_short Recent Advances in Treatments of Primary Focal Segmental Glomerulosclerosis in Children
title_sort recent advances in treatments of primary focal segmental glomerulosclerosis in children
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852325/
https://www.ncbi.nlm.nih.gov/pubmed/27195285
http://dx.doi.org/10.1155/2016/3053706
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