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Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery
BACKGROUND: The lack of early biomarkers for acute kidney injury (AKI) seriously inhibits the initiation of preventive and therapeutic measures for this syndrome in a timely manner. We tested the hypothesis that insulin-like growth factor-binding protein 7 (IGFBP7) and tissue inhibitor of metallopro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208780/ https://www.ncbi.nlm.nih.gov/pubmed/25343505 http://dx.doi.org/10.1371/journal.pone.0110865 |
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author | Meersch, Melanie Schmidt, Christoph Van Aken, Hugo Rossaint, Jan Görlich, Dennis Stege, Dirk Malec, Edward Januszewska, Katarzyna Zarbock, Alexander |
author_facet | Meersch, Melanie Schmidt, Christoph Van Aken, Hugo Rossaint, Jan Görlich, Dennis Stege, Dirk Malec, Edward Januszewska, Katarzyna Zarbock, Alexander |
author_sort | Meersch, Melanie |
collection | PubMed |
description | BACKGROUND: The lack of early biomarkers for acute kidney injury (AKI) seriously inhibits the initiation of preventive and therapeutic measures for this syndrome in a timely manner. We tested the hypothesis that insulin-like growth factor-binding protein 7 (IGFBP7) and tissue inhibitor of metalloproteinases-2 (TIMP-2), both inducers of G1 cell cycle arrest, function as early biomarkers for AKI after congenital heart surgery with cardiopulmonary bypass (CPB). METHODS: We prospectively studied 51 children undergoing cardiac surgery with CPB. Serial urine samples were analyzed for [TIMP-2]•[IGFBP7]. The primary outcome measure was AKI defined by the pRIFLE criteria within 72 hours after surgery. RESULTS: 12 children (24%) developed AKI within 1.67 (SE 0.3) days after surgery. Children who developed AKI after cardiac surgery had a significant higher urinary [TIMP-2]•[IGFBP7] as early as 4 h after the procedure, compared to children who did not develop AKI (mean of 1.93 ((ng/ml)(2)/1000) (SE 0.4) vs 0.47 ((ng/ml)(2)/1000) (SE 0.1), respectively; p<0.05). Urinary [TIMP-2]•[IGFBP7] 4 hours following surgery demonstrated an area under the receiver-operating characteristic curve of 0.85. Sensitivity was 0.83, and specificity was 0.77 for a cutoff value of 0.70 ((ng/ml)(2)/1000). CONCLUSIONS: Urinary [TIMP-2]•[IGFBP7] represent sensitive, specific, and highly predictive early biomarkers for AKI after surgery for congenital heart disease. TRIAL REGISTRATION: www.germanctr.de/, DRKS00005062 |
format | Online Article Text |
id | pubmed-4208780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42087802014-10-27 Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery Meersch, Melanie Schmidt, Christoph Van Aken, Hugo Rossaint, Jan Görlich, Dennis Stege, Dirk Malec, Edward Januszewska, Katarzyna Zarbock, Alexander PLoS One Research Article BACKGROUND: The lack of early biomarkers for acute kidney injury (AKI) seriously inhibits the initiation of preventive and therapeutic measures for this syndrome in a timely manner. We tested the hypothesis that insulin-like growth factor-binding protein 7 (IGFBP7) and tissue inhibitor of metalloproteinases-2 (TIMP-2), both inducers of G1 cell cycle arrest, function as early biomarkers for AKI after congenital heart surgery with cardiopulmonary bypass (CPB). METHODS: We prospectively studied 51 children undergoing cardiac surgery with CPB. Serial urine samples were analyzed for [TIMP-2]•[IGFBP7]. The primary outcome measure was AKI defined by the pRIFLE criteria within 72 hours after surgery. RESULTS: 12 children (24%) developed AKI within 1.67 (SE 0.3) days after surgery. Children who developed AKI after cardiac surgery had a significant higher urinary [TIMP-2]•[IGFBP7] as early as 4 h after the procedure, compared to children who did not develop AKI (mean of 1.93 ((ng/ml)(2)/1000) (SE 0.4) vs 0.47 ((ng/ml)(2)/1000) (SE 0.1), respectively; p<0.05). Urinary [TIMP-2]•[IGFBP7] 4 hours following surgery demonstrated an area under the receiver-operating characteristic curve of 0.85. Sensitivity was 0.83, and specificity was 0.77 for a cutoff value of 0.70 ((ng/ml)(2)/1000). CONCLUSIONS: Urinary [TIMP-2]•[IGFBP7] represent sensitive, specific, and highly predictive early biomarkers for AKI after surgery for congenital heart disease. TRIAL REGISTRATION: www.germanctr.de/, DRKS00005062 Public Library of Science 2014-10-24 /pmc/articles/PMC4208780/ /pubmed/25343505 http://dx.doi.org/10.1371/journal.pone.0110865 Text en © 2014 Meersch 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Meersch, Melanie Schmidt, Christoph Van Aken, Hugo Rossaint, Jan Görlich, Dennis Stege, Dirk Malec, Edward Januszewska, Katarzyna Zarbock, Alexander Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery |
title | Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery |
title_full | Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery |
title_fullStr | Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery |
title_full_unstemmed | Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery |
title_short | Validation of Cell-Cycle Arrest Biomarkers for Acute Kidney Injury after Pediatric Cardiac Surgery |
title_sort | validation of cell-cycle arrest biomarkers for acute kidney injury after pediatric cardiac surgery |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208780/ https://www.ncbi.nlm.nih.gov/pubmed/25343505 http://dx.doi.org/10.1371/journal.pone.0110865 |
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