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Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation
BACKGROUND: Neutrophil gelatinase-associated lipocalin (NGAL) is a marker for acute kidney injury. We studied whether serum NGAL predicts delayed graft function (DGF) and recovery of kidney function after transplantation. METHODS: Serum NGAL was analyzed using commercial ELISA and point-of-care (POC...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122536/ https://www.ncbi.nlm.nih.gov/pubmed/25066815 http://dx.doi.org/10.1186/1471-2369-15-123 |
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author | Hollmen, Maria E Kyllönen, Lauri E Merenmies, Jussi Salmela, Kaija T |
author_facet | Hollmen, Maria E Kyllönen, Lauri E Merenmies, Jussi Salmela, Kaija T |
author_sort | Hollmen, Maria E |
collection | PubMed |
description | BACKGROUND: Neutrophil gelatinase-associated lipocalin (NGAL) is a marker for acute kidney injury. We studied whether serum NGAL predicts delayed graft function (DGF) and recovery of kidney function after transplantation. METHODS: Serum NGAL was analyzed using commercial ELISA and point-of-care (POC) (Triage®, Biosite) methods. Serum samples were collected from 176 consecutive, deceased-donor kidney recipients just before transplant surgery and on day 1 and 14 after transplantation. The first 132 samples were analyzed with both methods and the remaining samples with the POC method. RESULTS: The correlation between the ELISA and POC methods was 0.89, p < 0.0001 and hence the POC method was used for the remaining analyses. DGF was seen in 66/176 patients. Day 1 sNGAL was significantly higher in DGF (588 ng/ml, SD 189.6) compared to early graft function (355 ng/ml, SD 166.2, p < 0.0001) and this difference persisted on day 14. Day 1 sNGAL predicted DGF with an area under the curve (AUC) of 0.853 (CI 0.792-0.914, p < 0.0001). At the optimal cutoff level of 423 ng/ml the sensitivity was 87% and the specificity 77%. In a multivariate analysis, day 1 sNGAL emerged as an independent predictor of DGF. The sNGAL also predicted DGF lasting longer than 14 days with an AUC of 0.825 (CI 0.751-0.899, p < 0.0001). At the optimal cutoff level of 486 ng/ml, the sensitivity was 80% and specificity 75%. CONCLUSION: Serum NGAL predicts clinically significant DGF and is useful in the care of kidney transplant recipients. |
format | Online Article Text |
id | pubmed-4122536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41225362014-08-06 Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation Hollmen, Maria E Kyllönen, Lauri E Merenmies, Jussi Salmela, Kaija T BMC Nephrol Research Article BACKGROUND: Neutrophil gelatinase-associated lipocalin (NGAL) is a marker for acute kidney injury. We studied whether serum NGAL predicts delayed graft function (DGF) and recovery of kidney function after transplantation. METHODS: Serum NGAL was analyzed using commercial ELISA and point-of-care (POC) (Triage®, Biosite) methods. Serum samples were collected from 176 consecutive, deceased-donor kidney recipients just before transplant surgery and on day 1 and 14 after transplantation. The first 132 samples were analyzed with both methods and the remaining samples with the POC method. RESULTS: The correlation between the ELISA and POC methods was 0.89, p < 0.0001 and hence the POC method was used for the remaining analyses. DGF was seen in 66/176 patients. Day 1 sNGAL was significantly higher in DGF (588 ng/ml, SD 189.6) compared to early graft function (355 ng/ml, SD 166.2, p < 0.0001) and this difference persisted on day 14. Day 1 sNGAL predicted DGF with an area under the curve (AUC) of 0.853 (CI 0.792-0.914, p < 0.0001). At the optimal cutoff level of 423 ng/ml the sensitivity was 87% and the specificity 77%. In a multivariate analysis, day 1 sNGAL emerged as an independent predictor of DGF. The sNGAL also predicted DGF lasting longer than 14 days with an AUC of 0.825 (CI 0.751-0.899, p < 0.0001). At the optimal cutoff level of 486 ng/ml, the sensitivity was 80% and specificity 75%. CONCLUSION: Serum NGAL predicts clinically significant DGF and is useful in the care of kidney transplant recipients. BioMed Central 2014-07-28 /pmc/articles/PMC4122536/ /pubmed/25066815 http://dx.doi.org/10.1186/1471-2369-15-123 Text en Copyright © 2014 Hollmen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Research Article Hollmen, Maria E Kyllönen, Lauri E Merenmies, Jussi Salmela, Kaija T Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation |
title | Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation |
title_full | Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation |
title_fullStr | Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation |
title_full_unstemmed | Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation |
title_short | Serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation |
title_sort | serum neutrophil gelatinase-associated lipocalin and recovery of kidney graft function after transplantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122536/ https://www.ncbi.nlm.nih.gov/pubmed/25066815 http://dx.doi.org/10.1186/1471-2369-15-123 |
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