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Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report
BACKGROUND: The proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor evolocumab is a low-density lipoprotein (LDL)-lowering drug with a new mechanism, which is currently available in Japan. Here, for the first time, we report the successful use of the PCSK9 inhibitor in a patient with ref...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501341/ https://www.ncbi.nlm.nih.gov/pubmed/28683788 http://dx.doi.org/10.1186/s12882-017-0644-0 |
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author | Awanami, Yuki Fukuda, Makoto Nonaka, Yasunori Takashima, Tsuyoshi Matsumoto, Keiichiro Yamasaki, Masatora Miyazono, Motoaki Ikeda, Yuji |
author_facet | Awanami, Yuki Fukuda, Makoto Nonaka, Yasunori Takashima, Tsuyoshi Matsumoto, Keiichiro Yamasaki, Masatora Miyazono, Motoaki Ikeda, Yuji |
author_sort | Awanami, Yuki |
collection | PubMed |
description | BACKGROUND: The proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor evolocumab is a low-density lipoprotein (LDL)-lowering drug with a new mechanism, which is currently available in Japan. Here, for the first time, we report the successful use of the PCSK9 inhibitor in a patient with refractory nephrotic syndrome. CASE PRESENTATION: A 61-year-old woman was diagnosed with minimal change-type nephrotic syndrome in October 2012. She received prednisolone (PSL) and cyclosporin A (CyA), but she experienced several cycles of relapse and remission and was hospitalized in May 2016 due to relapse. However, in spite of steroid pulse therapy and adrenocorticotropic hormone (ACTH) administration, her urinary protein level did not improve. We started her on evolocumab with the expectation of equivalent LDL-lowering effects as seen with LDL apheresis. After that, the LDL cholesterol level and UP/UC were concomitantly decreased, and the serum albumin was increased. This was maintained even when we reduced the PSL dose. This suggests that evolocumab clinically improves the nephrotic condition. CONCLUSION: No other report has described the use of evolocumab for nephrotic syndrome (NS) or its effect on similar nephrotic conditions. We believe that the findings presented here are unique and may be beneficial when treating similar cases. |
format | Online Article Text |
id | pubmed-5501341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55013412017-07-10 Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report Awanami, Yuki Fukuda, Makoto Nonaka, Yasunori Takashima, Tsuyoshi Matsumoto, Keiichiro Yamasaki, Masatora Miyazono, Motoaki Ikeda, Yuji BMC Nephrol Case Report BACKGROUND: The proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor evolocumab is a low-density lipoprotein (LDL)-lowering drug with a new mechanism, which is currently available in Japan. Here, for the first time, we report the successful use of the PCSK9 inhibitor in a patient with refractory nephrotic syndrome. CASE PRESENTATION: A 61-year-old woman was diagnosed with minimal change-type nephrotic syndrome in October 2012. She received prednisolone (PSL) and cyclosporin A (CyA), but she experienced several cycles of relapse and remission and was hospitalized in May 2016 due to relapse. However, in spite of steroid pulse therapy and adrenocorticotropic hormone (ACTH) administration, her urinary protein level did not improve. We started her on evolocumab with the expectation of equivalent LDL-lowering effects as seen with LDL apheresis. After that, the LDL cholesterol level and UP/UC were concomitantly decreased, and the serum albumin was increased. This was maintained even when we reduced the PSL dose. This suggests that evolocumab clinically improves the nephrotic condition. CONCLUSION: No other report has described the use of evolocumab for nephrotic syndrome (NS) or its effect on similar nephrotic conditions. We believe that the findings presented here are unique and may be beneficial when treating similar cases. BioMed Central 2017-07-06 /pmc/articles/PMC5501341/ /pubmed/28683788 http://dx.doi.org/10.1186/s12882-017-0644-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Awanami, Yuki Fukuda, Makoto Nonaka, Yasunori Takashima, Tsuyoshi Matsumoto, Keiichiro Yamasaki, Masatora Miyazono, Motoaki Ikeda, Yuji Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report |
title | Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report |
title_full | Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report |
title_fullStr | Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report |
title_full_unstemmed | Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report |
title_short | Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report |
title_sort | successful treatment of a patient with refractory nephrotic syndrome with pcsk9 inhibitors: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501341/ https://www.ncbi.nlm.nih.gov/pubmed/28683788 http://dx.doi.org/10.1186/s12882-017-0644-0 |
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