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Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release
Brain death (BD) is associated with a systemic inflammation leading to worse graft outcomes. This study aimed to compare plasma cytokine values between brain-dead and critically ill patients, including septic and non-septic controls, and evaluate cytokine release kinetics in BD. Sixteen brain-dead a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180721/ https://www.ncbi.nlm.nih.gov/pubmed/30235942 http://dx.doi.org/10.1177/0963689718785629 |
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author | Schwarz, Patrícia Custódio, Geisiane Rheinheimer, Jakeline Crispim, Daisy Leitão, Cristiane B. Rech, Tatiana H. |
author_facet | Schwarz, Patrícia Custódio, Geisiane Rheinheimer, Jakeline Crispim, Daisy Leitão, Cristiane B. Rech, Tatiana H. |
author_sort | Schwarz, Patrícia |
collection | PubMed |
description | Brain death (BD) is associated with a systemic inflammation leading to worse graft outcomes. This study aimed to compare plasma cytokine values between brain-dead and critically ill patients, including septic and non-septic controls, and evaluate cytokine release kinetics in BD. Sixteen brain-dead and 32 control patients (16 with and 16 without sepsis) were included. Plasma cytokines were measured by magnetic bead assay after the first clinical exam consistent with BD and every 6 hours thereafter, and at the time of study entry in the control group. The values for IL-8 and IFN-γ were higher in brain-dead and septic patients than in non-septic patients [IL-8: 80.3 (18.7–169.6) vs. 68.2 (22.4–359.4) vs. 16.4 (9.2–42.7) pg/mL; P = 0.006; IFN-γ: 2.8 (1.6-6.1) vs. 3.4 (1.2–9.0) vs. 0.5 (0.5–1.8) pg/mL; P = 0.012]. TNF showed a clear tendency to increase in brain-dead patients [2.7 (1.0–4.8) vs. 1.0 (1.0–5.6) vs. 1.0 (1.0–1.0) pg/mL; P = 0.051], and IL-6 values were higher in brain-dead patients than in non-septic controls [174.5 (104.9–692.5) vs. 13.2 (7.3–38.6) pg/mL; P = 0.002]. These differences remained even after excluding brain-dead patients who also had sepsis (n = 3). IL-1β and IL-10 values increased from baseline to time point 2 (∼6 hours later) [IL-1β: 5.39 (1.93–16.89) vs. 7.11 (1.93–29.13) pg/mL; P = 0.012; IL-10: 8.78 (3.62–16.49) vs. 15.73 (5.49–23.98) pg/mL; P = 0.009]. BD-induced and sepsis-induced plasma cytokine values were similarly high, and both were higher than the observed in non-septic critically ill patients. |
format | Online Article Text |
id | pubmed-6180721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61807212018-10-19 Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release Schwarz, Patrícia Custódio, Geisiane Rheinheimer, Jakeline Crispim, Daisy Leitão, Cristiane B. Rech, Tatiana H. Cell Transplant Original Articles Brain death (BD) is associated with a systemic inflammation leading to worse graft outcomes. This study aimed to compare plasma cytokine values between brain-dead and critically ill patients, including septic and non-septic controls, and evaluate cytokine release kinetics in BD. Sixteen brain-dead and 32 control patients (16 with and 16 without sepsis) were included. Plasma cytokines were measured by magnetic bead assay after the first clinical exam consistent with BD and every 6 hours thereafter, and at the time of study entry in the control group. The values for IL-8 and IFN-γ were higher in brain-dead and septic patients than in non-septic patients [IL-8: 80.3 (18.7–169.6) vs. 68.2 (22.4–359.4) vs. 16.4 (9.2–42.7) pg/mL; P = 0.006; IFN-γ: 2.8 (1.6-6.1) vs. 3.4 (1.2–9.0) vs. 0.5 (0.5–1.8) pg/mL; P = 0.012]. TNF showed a clear tendency to increase in brain-dead patients [2.7 (1.0–4.8) vs. 1.0 (1.0–5.6) vs. 1.0 (1.0–1.0) pg/mL; P = 0.051], and IL-6 values were higher in brain-dead patients than in non-septic controls [174.5 (104.9–692.5) vs. 13.2 (7.3–38.6) pg/mL; P = 0.002]. These differences remained even after excluding brain-dead patients who also had sepsis (n = 3). IL-1β and IL-10 values increased from baseline to time point 2 (∼6 hours later) [IL-1β: 5.39 (1.93–16.89) vs. 7.11 (1.93–29.13) pg/mL; P = 0.012; IL-10: 8.78 (3.62–16.49) vs. 15.73 (5.49–23.98) pg/mL; P = 0.009]. BD-induced and sepsis-induced plasma cytokine values were similarly high, and both were higher than the observed in non-septic critically ill patients. SAGE Publications 2018-09-20 2018-10 /pmc/articles/PMC6180721/ /pubmed/30235942 http://dx.doi.org/10.1177/0963689718785629 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Schwarz, Patrícia Custódio, Geisiane Rheinheimer, Jakeline Crispim, Daisy Leitão, Cristiane B. Rech, Tatiana H. Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release |
title | Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release |
title_full | Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release |
title_fullStr | Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release |
title_full_unstemmed | Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release |
title_short | Brain Death-Induced Inflammatory Activity is Similar to Sepsis-Induced Cytokine Release |
title_sort | brain death-induced inflammatory activity is similar to sepsis-induced cytokine release |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180721/ https://www.ncbi.nlm.nih.gov/pubmed/30235942 http://dx.doi.org/10.1177/0963689718785629 |
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