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Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients

BACKGROUND: Close monitoring of glomerular filtration rate (GFR) is essential for the management of patients post kidney transplantation. Measured GFR (mGFR), the gold standard, is not readily accessible in most centers. Furthermore, the performance of new estimated GFR (eGFR) equations based upon c...

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Autores principales: Meeusen, Jeffrey W., Stämmler, Frank, Dasari, Surendra, Schiffer, Eric, Lieske, John C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712186/
https://www.ncbi.nlm.nih.gov/pubmed/36465899
http://dx.doi.org/10.3389/fmed.2022.988989
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author Meeusen, Jeffrey W.
Stämmler, Frank
Dasari, Surendra
Schiffer, Eric
Lieske, John C.
author_facet Meeusen, Jeffrey W.
Stämmler, Frank
Dasari, Surendra
Schiffer, Eric
Lieske, John C.
author_sort Meeusen, Jeffrey W.
collection PubMed
description BACKGROUND: Close monitoring of glomerular filtration rate (GFR) is essential for the management of patients post kidney transplantation. Measured GFR (mGFR), the gold standard, is not readily accessible in most centers. Furthermore, the performance of new estimated GFR (eGFR) equations based upon creatinine and/or cystatin C have not been validated in kidney transplant patients. Here we evaluate a recently published eGFR equation using cystatin C, creatinine, myo-inositol and valine as measured by nuclear magnetic resonance (eGFR(NMR)). METHODS: Residual sera was obtained from a cohort of patients with clinically ordered iothalamate renal clearance mGFR (n = 602). Kidney transplant recipients accounted for 220 (37%) of participants. RESULTS: Compared to mGFR, there was no significant bias for eGFRcr or eGFR(NMR), while eGFRcr-cys significantly underestimated mGFR. P(30) values were similar for all eGFR. P(15) was significantly higher for eGFR(NMR) compared to eGFRcr, while the P(15) for eGFRcr-cys only improved among patients without a kidney transplant. Agreement with mGFR CKD stages of <15, 30, 45, 60, and 90 ml/min/1.73 m(2) was identical for eGFRcr and eGFRcr-cys (61.8%, both cases) while eGFR(NMR) was significantly higher (66.4%) among patients with a kidney transplant. CONCLUSION: The 2021 CKD-EPI eGFRcr and eGFRcr-cys have similar bias, P(15), and agreement while eGFR(NMR) more closely matched mGFR with the strongest improvement among kidney transplant recipients.
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spelling pubmed-97121862022-12-02 Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients Meeusen, Jeffrey W. Stämmler, Frank Dasari, Surendra Schiffer, Eric Lieske, John C. Front Med (Lausanne) Medicine BACKGROUND: Close monitoring of glomerular filtration rate (GFR) is essential for the management of patients post kidney transplantation. Measured GFR (mGFR), the gold standard, is not readily accessible in most centers. Furthermore, the performance of new estimated GFR (eGFR) equations based upon creatinine and/or cystatin C have not been validated in kidney transplant patients. Here we evaluate a recently published eGFR equation using cystatin C, creatinine, myo-inositol and valine as measured by nuclear magnetic resonance (eGFR(NMR)). METHODS: Residual sera was obtained from a cohort of patients with clinically ordered iothalamate renal clearance mGFR (n = 602). Kidney transplant recipients accounted for 220 (37%) of participants. RESULTS: Compared to mGFR, there was no significant bias for eGFRcr or eGFR(NMR), while eGFRcr-cys significantly underestimated mGFR. P(30) values were similar for all eGFR. P(15) was significantly higher for eGFR(NMR) compared to eGFRcr, while the P(15) for eGFRcr-cys only improved among patients without a kidney transplant. Agreement with mGFR CKD stages of <15, 30, 45, 60, and 90 ml/min/1.73 m(2) was identical for eGFRcr and eGFRcr-cys (61.8%, both cases) while eGFR(NMR) was significantly higher (66.4%) among patients with a kidney transplant. CONCLUSION: The 2021 CKD-EPI eGFRcr and eGFRcr-cys have similar bias, P(15), and agreement while eGFR(NMR) more closely matched mGFR with the strongest improvement among kidney transplant recipients. Frontiers Media S.A. 2022-11-17 /pmc/articles/PMC9712186/ /pubmed/36465899 http://dx.doi.org/10.3389/fmed.2022.988989 Text en Copyright © 2022 Meeusen, Stämmler, Dasari, Schiffer and Lieske. 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 Medicine
Meeusen, Jeffrey W.
Stämmler, Frank
Dasari, Surendra
Schiffer, Eric
Lieske, John C.
Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients
title Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients
title_full Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients
title_fullStr Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients
title_full_unstemmed Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients
title_short Serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients
title_sort serum myo-inositol and valine improve metabolomic-based estimated glomerular filtration rate among kidney transplant recipients
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712186/
https://www.ncbi.nlm.nih.gov/pubmed/36465899
http://dx.doi.org/10.3389/fmed.2022.988989
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