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Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study

BACKGROUND: Neuroinflammation is thought to play an important role in the pathogenesis of ICU-acquired delirium, but the association between inflammatory and brain-specific proteins and ICU delirium is poor. We investigated whether or not serial determinations of markers may improve this association...

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Autores principales: Simons, Koen S., van den Boogaard, Mark, Hendriksen, Eva, Gerretsen, Jelle, van der Hoeven, Johannes G., Pickkers, Peter, de Jager, Cornelis P. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970442/
https://www.ncbi.nlm.nih.gov/pubmed/29801516
http://dx.doi.org/10.1186/s13054-018-2054-5
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author Simons, Koen S.
van den Boogaard, Mark
Hendriksen, Eva
Gerretsen, Jelle
van der Hoeven, Johannes G.
Pickkers, Peter
de Jager, Cornelis P. C.
author_facet Simons, Koen S.
van den Boogaard, Mark
Hendriksen, Eva
Gerretsen, Jelle
van der Hoeven, Johannes G.
Pickkers, Peter
de Jager, Cornelis P. C.
author_sort Simons, Koen S.
collection PubMed
description BACKGROUND: Neuroinflammation is thought to play an important role in the pathogenesis of ICU-acquired delirium, but the association between inflammatory and brain-specific proteins and ICU delirium is poor. We investigated whether or not serial determinations of markers may improve this association. METHODS: Critically ill patients with a high risk of ICU delirium and with an ICU length of stay of at least 6 days were included in the study. Blood was drawn on days 1, 2, 4 and 6 after ICU admission and analyzed for different markers of inflammation and several brain proteins. Differences in courses over time prior to and following the onset of delirium and absolute differences over time were analyzed in patients with and without delirium using repeated measurement analysis of variance. In addition, a cross-sectional analysis of levels of these markers before the first onset of delirium was performed. RESULTS: Fifty patients were included in this study. In the longitudinal analysis, there were no differences in the levels of any of the markers immediately prior to and following the onset of delirium, but overall, median levels of adiponectin (9019 (IQR 5776–15,442) vs. 6148 (IQR 4447–8742) ng/ml, p = 0.05) were significantly higher in patients with delirium compared to patients without delirium. In the cross-sectional analysis, median levels of the brain protein Tau (90 (IQR 46–224) vs. 31 (IQR 31–52) pg/ml, p = 0.009) and the ratio Tau/amyloid β(1–42) (1.42 ((IQR 0.9–2.57) vs. 0.68 (IQR 0.54–0.96), p = 0.003) were significantly higher in patients with hypoactive delirium compared to patients without. Levels of neopterin (111 (IQR 37–111) vs. 29 (IQR 16–64) mmol/l, p = 0.004) and IL-10 (28 (IQR 12–39) vs. 9 (IQR 4–12) pg/ml, p = 0.001) were significantly higher in patients with hypoactive delirium compared to patients with mixed-type delirium. CONCLUSIONS: While there are differences in markers (adiponectin and several brain proteins) between patients with and without delirium, the development of delirium is not preceded by a change in the biomarker profile of inflammatory markers or brain proteins. Patients with hypoactive delirium account for the observed differences in biomarkers. TRIAL REGISTRATION: ClinicalTrials.gov, NCT 01274819. Registered on 12 January 2011. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2054-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-59704422018-05-30 Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study Simons, Koen S. van den Boogaard, Mark Hendriksen, Eva Gerretsen, Jelle van der Hoeven, Johannes G. Pickkers, Peter de Jager, Cornelis P. C. Crit Care Research BACKGROUND: Neuroinflammation is thought to play an important role in the pathogenesis of ICU-acquired delirium, but the association between inflammatory and brain-specific proteins and ICU delirium is poor. We investigated whether or not serial determinations of markers may improve this association. METHODS: Critically ill patients with a high risk of ICU delirium and with an ICU length of stay of at least 6 days were included in the study. Blood was drawn on days 1, 2, 4 and 6 after ICU admission and analyzed for different markers of inflammation and several brain proteins. Differences in courses over time prior to and following the onset of delirium and absolute differences over time were analyzed in patients with and without delirium using repeated measurement analysis of variance. In addition, a cross-sectional analysis of levels of these markers before the first onset of delirium was performed. RESULTS: Fifty patients were included in this study. In the longitudinal analysis, there were no differences in the levels of any of the markers immediately prior to and following the onset of delirium, but overall, median levels of adiponectin (9019 (IQR 5776–15,442) vs. 6148 (IQR 4447–8742) ng/ml, p = 0.05) were significantly higher in patients with delirium compared to patients without delirium. In the cross-sectional analysis, median levels of the brain protein Tau (90 (IQR 46–224) vs. 31 (IQR 31–52) pg/ml, p = 0.009) and the ratio Tau/amyloid β(1–42) (1.42 ((IQR 0.9–2.57) vs. 0.68 (IQR 0.54–0.96), p = 0.003) were significantly higher in patients with hypoactive delirium compared to patients without. Levels of neopterin (111 (IQR 37–111) vs. 29 (IQR 16–64) mmol/l, p = 0.004) and IL-10 (28 (IQR 12–39) vs. 9 (IQR 4–12) pg/ml, p = 0.001) were significantly higher in patients with hypoactive delirium compared to patients with mixed-type delirium. CONCLUSIONS: While there are differences in markers (adiponectin and several brain proteins) between patients with and without delirium, the development of delirium is not preceded by a change in the biomarker profile of inflammatory markers or brain proteins. Patients with hypoactive delirium account for the observed differences in biomarkers. TRIAL REGISTRATION: ClinicalTrials.gov, NCT 01274819. Registered on 12 January 2011. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2054-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-25 /pmc/articles/PMC5970442/ /pubmed/29801516 http://dx.doi.org/10.1186/s13054-018-2054-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Simons, Koen S.
van den Boogaard, Mark
Hendriksen, Eva
Gerretsen, Jelle
van der Hoeven, Johannes G.
Pickkers, Peter
de Jager, Cornelis P. C.
Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study
title Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study
title_full Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study
title_fullStr Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study
title_full_unstemmed Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study
title_short Temporal biomarker profiles and their association with ICU acquired delirium: a cohort study
title_sort temporal biomarker profiles and their association with icu acquired delirium: a cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970442/
https://www.ncbi.nlm.nih.gov/pubmed/29801516
http://dx.doi.org/10.1186/s13054-018-2054-5
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