Cargando…
Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study
INTRODUCTION: Expanding the criteria for deceased organ donors increases the risk of delayed graft function (DGF) and complicates kidney transplant outcome. We studied whether donor neutrophil gelatinase-associated lipocalin (NGAL), a novel biomarker for acute kidney injury, could predict DGF after...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218974/ https://www.ncbi.nlm.nih.gov/pubmed/21545740 http://dx.doi.org/10.1186/cc10220 |
_version_ | 1782216770024636416 |
---|---|
author | Hollmen, Maria E Kyllönen, Lauri E Inkinen, Kaija A Lalla, Martti LT Merenmies, Jussi Salmela, Kaija T |
author_facet | Hollmen, Maria E Kyllönen, Lauri E Inkinen, Kaija A Lalla, Martti LT Merenmies, Jussi Salmela, Kaija T |
author_sort | Hollmen, Maria E |
collection | PubMed |
description | INTRODUCTION: Expanding the criteria for deceased organ donors increases the risk of delayed graft function (DGF) and complicates kidney transplant outcome. We studied whether donor neutrophil gelatinase-associated lipocalin (NGAL), a novel biomarker for acute kidney injury, could predict DGF after transplantation. METHODS: We included 99 consecutive, deceased donors and their 176 kidney recipients. For NGAL detection, donor serum and urine samples were collected before the donor operation. The samples were analyzed using a commercial enzyme-linked immunosorbent assay kit (serum) and the ARCHITECT method (urine). RESULTS: Mean donor serum NGAL (S-NGAL) concentration was 218 ng/mL (range 27 to 658, standard deviation (SD) 145.1) and mean donor urine NGAL (U-NGAL) concentration was 18 ng/mL (range 0 to 177, SD 27.1). Donor S-NGAL and U-NGAL concentrations correlated directly with donor plasma creatinine levels and indirectly with estimated glomerular filtration rate (eGFR) calculated using the modification of diet in renal disease equation for glomerular filtration rate. In transplantations with high (greater than the mean) donor U-NGAL concentrations, prolonged DGF lasting longer than 14 days occurred more often than in transplantations with low (less than the mean) U-NGAL concentration (23% vs. 11%, P = 0.028), and 1-year graft survival was worse (90.3% vs. 97.4%, P = 0.048). High U-NGAL concentration was also associated with significantly more histological changes in the donor kidney biopsies than the low U-NGAL concentration. In a multivariate analysis, U-NGAL, expanded criteria donor status and eGFR emerged as independent risk factors for prolonged DGF. U-NGAL concentration failed to predict DGF on the basis of receiver operating characteristic curve analysis. CONCLUSIONS: This first report on S-NGAL and U-NGAL levels in deceased donors shows that donor U-NGAL, but not donor S-NGAL, measurements give added value when evaluating the suitability of a potential deceased kidney donor. |
format | Online Article Text |
id | pubmed-3218974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32189742011-11-17 Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study Hollmen, Maria E Kyllönen, Lauri E Inkinen, Kaija A Lalla, Martti LT Merenmies, Jussi Salmela, Kaija T Crit Care Research INTRODUCTION: Expanding the criteria for deceased organ donors increases the risk of delayed graft function (DGF) and complicates kidney transplant outcome. We studied whether donor neutrophil gelatinase-associated lipocalin (NGAL), a novel biomarker for acute kidney injury, could predict DGF after transplantation. METHODS: We included 99 consecutive, deceased donors and their 176 kidney recipients. For NGAL detection, donor serum and urine samples were collected before the donor operation. The samples were analyzed using a commercial enzyme-linked immunosorbent assay kit (serum) and the ARCHITECT method (urine). RESULTS: Mean donor serum NGAL (S-NGAL) concentration was 218 ng/mL (range 27 to 658, standard deviation (SD) 145.1) and mean donor urine NGAL (U-NGAL) concentration was 18 ng/mL (range 0 to 177, SD 27.1). Donor S-NGAL and U-NGAL concentrations correlated directly with donor plasma creatinine levels and indirectly with estimated glomerular filtration rate (eGFR) calculated using the modification of diet in renal disease equation for glomerular filtration rate. In transplantations with high (greater than the mean) donor U-NGAL concentrations, prolonged DGF lasting longer than 14 days occurred more often than in transplantations with low (less than the mean) U-NGAL concentration (23% vs. 11%, P = 0.028), and 1-year graft survival was worse (90.3% vs. 97.4%, P = 0.048). High U-NGAL concentration was also associated with significantly more histological changes in the donor kidney biopsies than the low U-NGAL concentration. In a multivariate analysis, U-NGAL, expanded criteria donor status and eGFR emerged as independent risk factors for prolonged DGF. U-NGAL concentration failed to predict DGF on the basis of receiver operating characteristic curve analysis. CONCLUSIONS: This first report on S-NGAL and U-NGAL levels in deceased donors shows that donor U-NGAL, but not donor S-NGAL, measurements give added value when evaluating the suitability of a potential deceased kidney donor. BioMed Central 2011 2011-05-05 /pmc/articles/PMC3218974/ /pubmed/21545740 http://dx.doi.org/10.1186/cc10220 Text en Copyright ©2011 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 cited |
spellingShingle | Research Hollmen, Maria E Kyllönen, Lauri E Inkinen, Kaija A Lalla, Martti LT Merenmies, Jussi Salmela, Kaija T Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study |
title | Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study |
title_full | Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study |
title_fullStr | Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study |
title_full_unstemmed | Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study |
title_short | Deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study |
title_sort | deceased donor neutrophil gelatinase-associated lipocalin and delayed graft function after kidney transplantation: a prospective study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218974/ https://www.ncbi.nlm.nih.gov/pubmed/21545740 http://dx.doi.org/10.1186/cc10220 |
work_keys_str_mv | AT hollmenmariae deceaseddonorneutrophilgelatinaseassociatedlipocalinanddelayedgraftfunctionafterkidneytransplantationaprospectivestudy AT kyllonenlaurie deceaseddonorneutrophilgelatinaseassociatedlipocalinanddelayedgraftfunctionafterkidneytransplantationaprospectivestudy AT inkinenkaijaa deceaseddonorneutrophilgelatinaseassociatedlipocalinanddelayedgraftfunctionafterkidneytransplantationaprospectivestudy AT lallamarttilt deceaseddonorneutrophilgelatinaseassociatedlipocalinanddelayedgraftfunctionafterkidneytransplantationaprospectivestudy AT merenmiesjussi deceaseddonorneutrophilgelatinaseassociatedlipocalinanddelayedgraftfunctionafterkidneytransplantationaprospectivestudy AT salmelakaijat deceaseddonorneutrophilgelatinaseassociatedlipocalinanddelayedgraftfunctionafterkidneytransplantationaprospectivestudy |