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Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C
Background: Accurate measurement of kidney function in patients with neuromuscular disorders is challenging. Cystatin C, a marker not influenced by skeletal muscle degradation, might be of clinical value in these patients. Methods: We consecutively enrolled 39 patients with neuromuscular disorders....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498206/ https://www.ncbi.nlm.nih.gov/pubmed/34630276 http://dx.doi.org/10.3389/fneur.2021.688246 |
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author | Screever, Elles M. Kootstra-Ros, Jenny E. Doorn, Joyce Nieuwenhuis, Jellie A. Meulenbelt, Henk E. J. Meijers, Wouter C. de Boer, Rudolf A. |
author_facet | Screever, Elles M. Kootstra-Ros, Jenny E. Doorn, Joyce Nieuwenhuis, Jellie A. Meulenbelt, Henk E. J. Meijers, Wouter C. de Boer, Rudolf A. |
author_sort | Screever, Elles M. |
collection | PubMed |
description | Background: Accurate measurement of kidney function in patients with neuromuscular disorders is challenging. Cystatin C, a marker not influenced by skeletal muscle degradation, might be of clinical value in these patients. Methods: We consecutively enrolled 39 patients with neuromuscular disorders. We investigated the association of the eGFR, based on plasma creatinine and Cystatin C, with clinical and biochemical variables associated with kidney function, namely age and galectin-3. Results: Creatinine-based eGFR was 242 (±80) and Cystatin C-based eGFR was 110 (±23) mL/min/1.73 m(2). Cystatin C-based eGFR was associated with age (β −0.63 p < 0.0001) and galectin-3 levels (β −0.43 p < 0.01), while creatinine-based eGFR was not (β −0.22 p = 0.20; β −0.28 p = 0.10). Sensitivity analyses in Duchenne and Becker patients revealed the same results: Cystatin C-based eGFR was associated with age (β −0.61 p < 0.01) and galectin-3 levels (β −0.43 p = 0.05), while creatinine-based eGFR was not (β −0.32 p = 0.13; β −0.34 p = 0.14). Conclusions: These data indicate that estimation of renal function in patients with neuromuscular disorders cannot reliably be achieved with creatinine, while Cystatin C appears a reasonable alternative. Since a large proportion of patients with neuromuscular disorders develops heart failure, and requires heart failure medication, adequate monitoring of renal function is warranted. |
format | Online Article Text |
id | pubmed-8498206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84982062021-10-09 Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C Screever, Elles M. Kootstra-Ros, Jenny E. Doorn, Joyce Nieuwenhuis, Jellie A. Meulenbelt, Henk E. J. Meijers, Wouter C. de Boer, Rudolf A. Front Neurol Neurology Background: Accurate measurement of kidney function in patients with neuromuscular disorders is challenging. Cystatin C, a marker not influenced by skeletal muscle degradation, might be of clinical value in these patients. Methods: We consecutively enrolled 39 patients with neuromuscular disorders. We investigated the association of the eGFR, based on plasma creatinine and Cystatin C, with clinical and biochemical variables associated with kidney function, namely age and galectin-3. Results: Creatinine-based eGFR was 242 (±80) and Cystatin C-based eGFR was 110 (±23) mL/min/1.73 m(2). Cystatin C-based eGFR was associated with age (β −0.63 p < 0.0001) and galectin-3 levels (β −0.43 p < 0.01), while creatinine-based eGFR was not (β −0.22 p = 0.20; β −0.28 p = 0.10). Sensitivity analyses in Duchenne and Becker patients revealed the same results: Cystatin C-based eGFR was associated with age (β −0.61 p < 0.01) and galectin-3 levels (β −0.43 p = 0.05), while creatinine-based eGFR was not (β −0.32 p = 0.13; β −0.34 p = 0.14). Conclusions: These data indicate that estimation of renal function in patients with neuromuscular disorders cannot reliably be achieved with creatinine, while Cystatin C appears a reasonable alternative. Since a large proportion of patients with neuromuscular disorders develops heart failure, and requires heart failure medication, adequate monitoring of renal function is warranted. Frontiers Media S.A. 2021-09-24 /pmc/articles/PMC8498206/ /pubmed/34630276 http://dx.doi.org/10.3389/fneur.2021.688246 Text en Copyright © 2021 Screever, Kootstra-Ros, Doorn, Nieuwenhuis, Meulenbelt, Meijers and de Boer. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Screever, Elles M. Kootstra-Ros, Jenny E. Doorn, Joyce Nieuwenhuis, Jellie A. Meulenbelt, Henk E. J. Meijers, Wouter C. de Boer, Rudolf A. Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C |
title | Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C |
title_full | Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C |
title_fullStr | Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C |
title_full_unstemmed | Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C |
title_short | Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C |
title_sort | kidney function in patients with neuromuscular disease: creatinine versus cystatin c |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498206/ https://www.ncbi.nlm.nih.gov/pubmed/34630276 http://dx.doi.org/10.3389/fneur.2021.688246 |
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