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Circulating cell-free DNA as a potential marker in smoke inhalation injury
Failure in evaluation of smoke inhalation injury (SII) is related to increased morbidity and mortality. Prognostic biomarkers that reflect the injury are undoubtedly needed. Cell-free DNA (CFD) concentrations are associated to the extent of tissue damage and inflammation in various pathologies. We h...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708904/ https://www.ncbi.nlm.nih.gov/pubmed/30896631 http://dx.doi.org/10.1097/MD.0000000000014863 |
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author | Hayun, Yehiel Shoham, Yaron Krieger, Yuval Silberstein, Eldad Douvdevani, Amos Ad-El, Dean |
author_facet | Hayun, Yehiel Shoham, Yaron Krieger, Yuval Silberstein, Eldad Douvdevani, Amos Ad-El, Dean |
author_sort | Hayun, Yehiel |
collection | PubMed |
description | Failure in evaluation of smoke inhalation injury (SII) is related to increased morbidity and mortality. Prognostic biomarkers that reflect the injury are undoubtedly needed. Cell-free DNA (CFD) concentrations are associated to the extent of tissue damage and inflammation in various pathologies. We have developed a simple assay for CFD quantification and previously found it prognostic in various pathologies including burns, lung disease, and sepsis. The aim of this study was to evaluate admission CFD as an injury severity marker in patients with SII. In a prospective study, we measured admission CFD levels in 18 SII patients and matched control subjects. Daily CFD levels were also performed in 4 hospitalized patients. Serum CFD levels were measured by our direct rapid fluorometric assay. Admission CFD levels of SII patients were significantly higher than those of healthy controls, 879 (236–3220) ng/mL vs. 339 (150–570) ng/mL, [median (range)], P < .0001. Admission CFD levels of hospitalized patients were significantly higher than those of nonhospitalized patients, 1517 (655–3220) ng/mL vs. 675 (236–1581) ng/mL, P < .05. Admission CFD positively correlated with hospitalization time (Rho = 0.578, P < .05) and was in linear correlation with CO poisoning (carboxyhemoglobin (COHb) levels, R(2) = 0.621, P < .0001). Additionally, along with the recovery of hospitalized patients, we observed a matched reduction of CFD levels. CFD appears to be a potentially valuable marker for severity and follow-up of SII. We believe this rapid assay can help introduce the routine use of CFD measurement into daily practice. |
format | Online Article Text |
id | pubmed-6708904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-67089042019-10-01 Circulating cell-free DNA as a potential marker in smoke inhalation injury Hayun, Yehiel Shoham, Yaron Krieger, Yuval Silberstein, Eldad Douvdevani, Amos Ad-El, Dean Medicine (Baltimore) Research Article Failure in evaluation of smoke inhalation injury (SII) is related to increased morbidity and mortality. Prognostic biomarkers that reflect the injury are undoubtedly needed. Cell-free DNA (CFD) concentrations are associated to the extent of tissue damage and inflammation in various pathologies. We have developed a simple assay for CFD quantification and previously found it prognostic in various pathologies including burns, lung disease, and sepsis. The aim of this study was to evaluate admission CFD as an injury severity marker in patients with SII. In a prospective study, we measured admission CFD levels in 18 SII patients and matched control subjects. Daily CFD levels were also performed in 4 hospitalized patients. Serum CFD levels were measured by our direct rapid fluorometric assay. Admission CFD levels of SII patients were significantly higher than those of healthy controls, 879 (236–3220) ng/mL vs. 339 (150–570) ng/mL, [median (range)], P < .0001. Admission CFD levels of hospitalized patients were significantly higher than those of nonhospitalized patients, 1517 (655–3220) ng/mL vs. 675 (236–1581) ng/mL, P < .05. Admission CFD positively correlated with hospitalization time (Rho = 0.578, P < .05) and was in linear correlation with CO poisoning (carboxyhemoglobin (COHb) levels, R(2) = 0.621, P < .0001). Additionally, along with the recovery of hospitalized patients, we observed a matched reduction of CFD levels. CFD appears to be a potentially valuable marker for severity and follow-up of SII. We believe this rapid assay can help introduce the routine use of CFD measurement into daily practice. Wolters Kluwer Health 2019-03-22 /pmc/articles/PMC6708904/ /pubmed/30896631 http://dx.doi.org/10.1097/MD.0000000000014863 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | Research Article Hayun, Yehiel Shoham, Yaron Krieger, Yuval Silberstein, Eldad Douvdevani, Amos Ad-El, Dean Circulating cell-free DNA as a potential marker in smoke inhalation injury |
title | Circulating cell-free DNA as a potential marker in smoke inhalation injury |
title_full | Circulating cell-free DNA as a potential marker in smoke inhalation injury |
title_fullStr | Circulating cell-free DNA as a potential marker in smoke inhalation injury |
title_full_unstemmed | Circulating cell-free DNA as a potential marker in smoke inhalation injury |
title_short | Circulating cell-free DNA as a potential marker in smoke inhalation injury |
title_sort | circulating cell-free dna as a potential marker in smoke inhalation injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708904/ https://www.ncbi.nlm.nih.gov/pubmed/30896631 http://dx.doi.org/10.1097/MD.0000000000014863 |
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