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Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study
BACKGROUND: Nephrotic syndrome (NS) results in massive proteinuria and hypoalbuminemia, which are responsible for a compensatory increase in protein synthesis in the liver. Serum cholinesterase (ChE) also increases in NS. However, its clinical value is not fully elucidated. METHODS: In this study, 1...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976987/ https://www.ncbi.nlm.nih.gov/pubmed/35366840 http://dx.doi.org/10.1186/s12882-022-02764-0 |
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author | Goto, Kimihiko Kono, Keiji Fujii, Hideki Goto, Shunsuke Nishi, Shinichi |
author_facet | Goto, Kimihiko Kono, Keiji Fujii, Hideki Goto, Shunsuke Nishi, Shinichi |
author_sort | Goto, Kimihiko |
collection | PubMed |
description | BACKGROUND: Nephrotic syndrome (NS) results in massive proteinuria and hypoalbuminemia, which are responsible for a compensatory increase in protein synthesis in the liver. Serum cholinesterase (ChE) also increases in NS. However, its clinical value is not fully elucidated. METHODS: In this study, 184 patients with NS who underwent kidney biopsy were included. The patients were divided into two groups according to serum ChE levels, as follows: hypercholinesterasemia (HC) and non-hypercholinesterasemia (NHC) groups. The clinical factors were compared between the two groups. RESULTS: The HC group had significantly more severe proteinuria and higher prevalence of high selective proteinuria than the NHC group. Furthermore, the prevalence of minimal change nephrotic syndrome (MCNS) was significantly higher in the HC group than that in the NHC group. Multivariate analysis revealed that the severity of proteinuria and MCNS were significantly associated with HC. CONCLUSION: In this study, HC in NS was associated with the severity of proteinuria and MCNS, and could help clinicians predict the histological diagnosis of NS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-022-02764-0. |
format | Online Article Text |
id | pubmed-8976987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89769872022-04-04 Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study Goto, Kimihiko Kono, Keiji Fujii, Hideki Goto, Shunsuke Nishi, Shinichi BMC Nephrol Research BACKGROUND: Nephrotic syndrome (NS) results in massive proteinuria and hypoalbuminemia, which are responsible for a compensatory increase in protein synthesis in the liver. Serum cholinesterase (ChE) also increases in NS. However, its clinical value is not fully elucidated. METHODS: In this study, 184 patients with NS who underwent kidney biopsy were included. The patients were divided into two groups according to serum ChE levels, as follows: hypercholinesterasemia (HC) and non-hypercholinesterasemia (NHC) groups. The clinical factors were compared between the two groups. RESULTS: The HC group had significantly more severe proteinuria and higher prevalence of high selective proteinuria than the NHC group. Furthermore, the prevalence of minimal change nephrotic syndrome (MCNS) was significantly higher in the HC group than that in the NHC group. Multivariate analysis revealed that the severity of proteinuria and MCNS were significantly associated with HC. CONCLUSION: In this study, HC in NS was associated with the severity of proteinuria and MCNS, and could help clinicians predict the histological diagnosis of NS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-022-02764-0. BioMed Central 2022-04-02 /pmc/articles/PMC8976987/ /pubmed/35366840 http://dx.doi.org/10.1186/s12882-022-02764-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Goto, Kimihiko Kono, Keiji Fujii, Hideki Goto, Shunsuke Nishi, Shinichi Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study |
title | Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study |
title_full | Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study |
title_fullStr | Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study |
title_full_unstemmed | Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study |
title_short | Clinical value of serum cholinesterase levels in Nephrotic syndrome: an observational study |
title_sort | clinical value of serum cholinesterase levels in nephrotic syndrome: an observational study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976987/ https://www.ncbi.nlm.nih.gov/pubmed/35366840 http://dx.doi.org/10.1186/s12882-022-02764-0 |
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