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External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury
BACKGROUND: Persistent acute kidney injury (AKI) portends worse clinical outcomes and remains a therapeutic challenge for clinicians. A recent study found that urinary C–C motif chemokine ligand 14 (CCL14) can predict the development of persistent AKI. We aimed to externally validate urinary CCL14 f...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166095/ https://www.ncbi.nlm.nih.gov/pubmed/34059102 http://dx.doi.org/10.1186/s13054-021-03618-1 |
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author | Bagshaw, Sean M. Al-Khafaji, Ali Artigas, Antonio Davison, Danielle Haase, Michael Lissauer, Matthew Zacharowski, Kai Chawla, Lakhmir S. Kwan, Thomas Kampf, J. Patrick McPherson, Paul Kellum, John A. |
author_facet | Bagshaw, Sean M. Al-Khafaji, Ali Artigas, Antonio Davison, Danielle Haase, Michael Lissauer, Matthew Zacharowski, Kai Chawla, Lakhmir S. Kwan, Thomas Kampf, J. Patrick McPherson, Paul Kellum, John A. |
author_sort | Bagshaw, Sean M. |
collection | PubMed |
description | BACKGROUND: Persistent acute kidney injury (AKI) portends worse clinical outcomes and remains a therapeutic challenge for clinicians. A recent study found that urinary C–C motif chemokine ligand 14 (CCL14) can predict the development of persistent AKI. We aimed to externally validate urinary CCL14 for the prediction of persistent AKI in critically ill patients. METHODS: This was a secondary analysis of the prospective multi-center SAPPHIRE study. We evaluated critically ill patients with cardiac and/or respiratory dysfunction who developed Kidney Disease: Improving Global Outcomes (KDIGO) stage 2–3 AKI within one week of enrollment. The main exposure was the urinary concentration of CCL14 measured at the onset of AKI stage 2–3. The primary endpoint was the development of persistent severe AKI, defined as ≥ 72 h of KDIGO stage 3 AKI or death or renal-replacement therapy (RRT) prior to 72 h. The secondary endpoint was a composite of RRT and/or death by 90 days. We used receiver operating characteristic (ROC) curve analysis to assess discriminative ability of urinary CCL14 for the development of persistent severe AKI and multivariate analysis to compare tertiles of urinary CCL14 and outcomes. RESULTS: We included 195 patients who developed KDIGO stage 2–3 AKI. Of these, 28 (14%) developed persistent severe AKI, of whom 15 had AKI ≥ 72 h, 12 received RRT and 1 died prior to ≥ 72 h of KDIGO stage 3 AKI. Persistent severe AKI was associated with chronic kidney disease, diabetes mellitus, higher non-renal APACHE III score, greater fluid balance, vasopressor use, and greater change in baseline serum creatinine. The AUC for urinary CCL14 to predict persistent severe AKI was 0.81 (95% CI, 0.72–0.89). The risk of persistent severe AKI increased with higher values of urinary CCL14. RRT and/or death at 90 days increased within tertiles of urinary CCL14 concentration. CONCLUSIONS: This secondary analysis externally validates urinary CCL14 to predict persistent severe AKI in critically ill patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03618-1. |
format | Online Article Text |
id | pubmed-8166095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81660952021-06-02 External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury Bagshaw, Sean M. Al-Khafaji, Ali Artigas, Antonio Davison, Danielle Haase, Michael Lissauer, Matthew Zacharowski, Kai Chawla, Lakhmir S. Kwan, Thomas Kampf, J. Patrick McPherson, Paul Kellum, John A. Crit Care Research BACKGROUND: Persistent acute kidney injury (AKI) portends worse clinical outcomes and remains a therapeutic challenge for clinicians. A recent study found that urinary C–C motif chemokine ligand 14 (CCL14) can predict the development of persistent AKI. We aimed to externally validate urinary CCL14 for the prediction of persistent AKI in critically ill patients. METHODS: This was a secondary analysis of the prospective multi-center SAPPHIRE study. We evaluated critically ill patients with cardiac and/or respiratory dysfunction who developed Kidney Disease: Improving Global Outcomes (KDIGO) stage 2–3 AKI within one week of enrollment. The main exposure was the urinary concentration of CCL14 measured at the onset of AKI stage 2–3. The primary endpoint was the development of persistent severe AKI, defined as ≥ 72 h of KDIGO stage 3 AKI or death or renal-replacement therapy (RRT) prior to 72 h. The secondary endpoint was a composite of RRT and/or death by 90 days. We used receiver operating characteristic (ROC) curve analysis to assess discriminative ability of urinary CCL14 for the development of persistent severe AKI and multivariate analysis to compare tertiles of urinary CCL14 and outcomes. RESULTS: We included 195 patients who developed KDIGO stage 2–3 AKI. Of these, 28 (14%) developed persistent severe AKI, of whom 15 had AKI ≥ 72 h, 12 received RRT and 1 died prior to ≥ 72 h of KDIGO stage 3 AKI. Persistent severe AKI was associated with chronic kidney disease, diabetes mellitus, higher non-renal APACHE III score, greater fluid balance, vasopressor use, and greater change in baseline serum creatinine. The AUC for urinary CCL14 to predict persistent severe AKI was 0.81 (95% CI, 0.72–0.89). The risk of persistent severe AKI increased with higher values of urinary CCL14. RRT and/or death at 90 days increased within tertiles of urinary CCL14 concentration. CONCLUSIONS: This secondary analysis externally validates urinary CCL14 to predict persistent severe AKI in critically ill patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03618-1. BioMed Central 2021-05-31 /pmc/articles/PMC8166095/ /pubmed/34059102 http://dx.doi.org/10.1186/s13054-021-03618-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Bagshaw, Sean M. Al-Khafaji, Ali Artigas, Antonio Davison, Danielle Haase, Michael Lissauer, Matthew Zacharowski, Kai Chawla, Lakhmir S. Kwan, Thomas Kampf, J. Patrick McPherson, Paul Kellum, John A. External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury |
title | External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury |
title_full | External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury |
title_fullStr | External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury |
title_full_unstemmed | External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury |
title_short | External validation of urinary C–C motif chemokine ligand 14 (CCL14) for prediction of persistent acute kidney injury |
title_sort | external validation of urinary c–c motif chemokine ligand 14 (ccl14) for prediction of persistent acute kidney injury |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166095/ https://www.ncbi.nlm.nih.gov/pubmed/34059102 http://dx.doi.org/10.1186/s13054-021-03618-1 |
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