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P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study
BACKGROUND: Early markers to predict delayed kidney graft function (DGF) may support clinical management. We studied the ability of four biomarkers (neutrophil gelatinase associated lipocalin (NGAL), liver-type fatty acid-binding protein (L-FABP), cystatin C, and YKL-40) to predict DGF after decease...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394926/ https://www.ncbi.nlm.nih.gov/pubmed/30817778 http://dx.doi.org/10.1371/journal.pone.0212676 |
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author | Nielsen, Marie B. Krogstrup, Nicoline V. Nieuwenhuijs-Moeke, Gertrude J. Oltean, Mihai Dor, Frank J. M. F. Jespersen, Bente Birn, Henrik |
author_facet | Nielsen, Marie B. Krogstrup, Nicoline V. Nieuwenhuijs-Moeke, Gertrude J. Oltean, Mihai Dor, Frank J. M. F. Jespersen, Bente Birn, Henrik |
author_sort | Nielsen, Marie B. |
collection | PubMed |
description | BACKGROUND: Early markers to predict delayed kidney graft function (DGF) may support clinical management. We studied the ability of four biomarkers (neutrophil gelatinase associated lipocalin (NGAL), liver-type fatty acid-binding protein (L-FABP), cystatin C, and YKL-40) to predict DGF after deceased donor transplantation, and their association with early graft function and GFR at three and twelve months. METHODS: 225 deceased donor kidney transplant recipients were included. Biomarkers were measured using automated assays or ELISA. We calculated their ability to predict the need for dialysis post-transplant and correlated with the estimated time to a 50% reduction in plasma creatinine (tCr50), measured glomerular filtration rate (mGFR) and estimated GFR (eGFR). RESULTS: All biomarkers measured at Day 1, except urinary L-FABP, significantly correlated with tCr50 and mGFR at Day 5. Plasma NGAL at Day 1 and a timed urine output predicted DGF (AUC = 0.91 and AUC 0.98). Nil or only weak correlations were identified between early biomarker levels and mGFR or eGFR at three or twelve months. CONCLUSION: High plasma NGAL at Day 1 predicts DGF and is associated with initial graft function, but may not prove better than P-creatinine or a timed urine output. Early biomarker levels do not correlate with one-year graft function. TRIAL REGISTRATION: ClinicalTrials.gov NCT01395719 |
format | Online Article Text |
id | pubmed-6394926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63949262019-03-08 P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study Nielsen, Marie B. Krogstrup, Nicoline V. Nieuwenhuijs-Moeke, Gertrude J. Oltean, Mihai Dor, Frank J. M. F. Jespersen, Bente Birn, Henrik PLoS One Research Article BACKGROUND: Early markers to predict delayed kidney graft function (DGF) may support clinical management. We studied the ability of four biomarkers (neutrophil gelatinase associated lipocalin (NGAL), liver-type fatty acid-binding protein (L-FABP), cystatin C, and YKL-40) to predict DGF after deceased donor transplantation, and their association with early graft function and GFR at three and twelve months. METHODS: 225 deceased donor kidney transplant recipients were included. Biomarkers were measured using automated assays or ELISA. We calculated their ability to predict the need for dialysis post-transplant and correlated with the estimated time to a 50% reduction in plasma creatinine (tCr50), measured glomerular filtration rate (mGFR) and estimated GFR (eGFR). RESULTS: All biomarkers measured at Day 1, except urinary L-FABP, significantly correlated with tCr50 and mGFR at Day 5. Plasma NGAL at Day 1 and a timed urine output predicted DGF (AUC = 0.91 and AUC 0.98). Nil or only weak correlations were identified between early biomarker levels and mGFR or eGFR at three or twelve months. CONCLUSION: High plasma NGAL at Day 1 predicts DGF and is associated with initial graft function, but may not prove better than P-creatinine or a timed urine output. Early biomarker levels do not correlate with one-year graft function. TRIAL REGISTRATION: ClinicalTrials.gov NCT01395719 Public Library of Science 2019-02-28 /pmc/articles/PMC6394926/ /pubmed/30817778 http://dx.doi.org/10.1371/journal.pone.0212676 Text en © 2019 Nielsen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Nielsen, Marie B. Krogstrup, Nicoline V. Nieuwenhuijs-Moeke, Gertrude J. Oltean, Mihai Dor, Frank J. M. F. Jespersen, Bente Birn, Henrik P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study |
title | P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study |
title_full | P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study |
title_fullStr | P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study |
title_full_unstemmed | P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study |
title_short | P-NGAL Day 1 predicts early but not one year graft function following deceased donor kidney transplantation – The CONTEXT study |
title_sort | p-ngal day 1 predicts early but not one year graft function following deceased donor kidney transplantation – the context study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394926/ https://www.ncbi.nlm.nih.gov/pubmed/30817778 http://dx.doi.org/10.1371/journal.pone.0212676 |
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