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The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy
We investigated the role of dynamic changes of serum levels S100B protein in brain injury and poor outcome of sepsis. This is a prospective cohort study designed to include 104 adult patients with sepsis who are admitted to ICU from Jan 2015 to Aug 2016. Sepsis was defined as sepsis 3.0. Patients wi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206038/ https://www.ncbi.nlm.nih.gov/pubmed/32382007 http://dx.doi.org/10.1038/s41598-020-64200-3 |
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author | Wu, Long Feng, Qing Ai, Mei-Lin Deng, Song-yun Liu, Zhi-Yong Huang, Li Ai, Yu-Hang Zhang, Lina |
author_facet | Wu, Long Feng, Qing Ai, Mei-Lin Deng, Song-yun Liu, Zhi-Yong Huang, Li Ai, Yu-Hang Zhang, Lina |
author_sort | Wu, Long |
collection | PubMed |
description | We investigated the role of dynamic changes of serum levels S100B protein in brain injury and poor outcome of sepsis. This is a prospective cohort study designed to include 104 adult patients with sepsis who are admitted to ICU from Jan 2015 to Aug 2016. Sepsis was defined as sepsis 3.0. Patients with a GCS score of <15, or at least one positive CAM-ICU score were thought to have brain dysfunction. 59 patients were diagnosed with SAE and the rest 45 patients were diagnosed with non-SAE. Serum S100B was measured on day 1 and 3 after ICU admission. Primary outcomes included brain dysfunction and 28-day/180-day mortality. The SAE group showed a significantly higher APACHE II score, SOFA scores, length of ICU stay, 28-day and 180-day mortality, serum S100B levels on day 1 and day 3. S100B levels on day 1 of 0.226 μg/L were diagnostic for SAE with 80.0% specificity and 66.1% sensitivity, and the area under (AUC) the curve was 0.728, S100B levels on day 3 of 0.144 μg/L were diagnostic for SAE with 84.44% specificity and 69.49% sensitivity, and the AUC was 0.819. In addition, the AUC for S100B on day 3 for predicting 180-day mortality was larger than for S100B on day 1 (0.731 vs. 0.611). Multiple logistic regression analysis showed that S100B3 (p = 0.001) but not S100B1 (p = 0.927) were independently correlated with SAE. Kaplan-Meier survival analysis showed that patients with S100B levels higher than 0.144 μg/L had a lower probability of survival at day 180. There were more patients with encephalopathy and a higher 28-day or 180-day mortality in the ΔS100B + group than in the ΔS100B- group. Multiple logistic regression analysis showed that SAE and IL-6 on day 3 were independently correlated with S100B dynamic increase. These findings suggest that elevated serum S100B levels on day 3 and the dynamic changes of serum S100B levels from day three to one were more associated with brain dysfunction and mortality than that on day 1 in patients with sepsis. |
format | Online Article Text |
id | pubmed-7206038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72060382020-05-15 The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy Wu, Long Feng, Qing Ai, Mei-Lin Deng, Song-yun Liu, Zhi-Yong Huang, Li Ai, Yu-Hang Zhang, Lina Sci Rep Article We investigated the role of dynamic changes of serum levels S100B protein in brain injury and poor outcome of sepsis. This is a prospective cohort study designed to include 104 adult patients with sepsis who are admitted to ICU from Jan 2015 to Aug 2016. Sepsis was defined as sepsis 3.0. Patients with a GCS score of <15, or at least one positive CAM-ICU score were thought to have brain dysfunction. 59 patients were diagnosed with SAE and the rest 45 patients were diagnosed with non-SAE. Serum S100B was measured on day 1 and 3 after ICU admission. Primary outcomes included brain dysfunction and 28-day/180-day mortality. The SAE group showed a significantly higher APACHE II score, SOFA scores, length of ICU stay, 28-day and 180-day mortality, serum S100B levels on day 1 and day 3. S100B levels on day 1 of 0.226 μg/L were diagnostic for SAE with 80.0% specificity and 66.1% sensitivity, and the area under (AUC) the curve was 0.728, S100B levels on day 3 of 0.144 μg/L were diagnostic for SAE with 84.44% specificity and 69.49% sensitivity, and the AUC was 0.819. In addition, the AUC for S100B on day 3 for predicting 180-day mortality was larger than for S100B on day 1 (0.731 vs. 0.611). Multiple logistic regression analysis showed that S100B3 (p = 0.001) but not S100B1 (p = 0.927) were independently correlated with SAE. Kaplan-Meier survival analysis showed that patients with S100B levels higher than 0.144 μg/L had a lower probability of survival at day 180. There were more patients with encephalopathy and a higher 28-day or 180-day mortality in the ΔS100B + group than in the ΔS100B- group. Multiple logistic regression analysis showed that SAE and IL-6 on day 3 were independently correlated with S100B dynamic increase. These findings suggest that elevated serum S100B levels on day 3 and the dynamic changes of serum S100B levels from day three to one were more associated with brain dysfunction and mortality than that on day 1 in patients with sepsis. Nature Publishing Group UK 2020-05-07 /pmc/articles/PMC7206038/ /pubmed/32382007 http://dx.doi.org/10.1038/s41598-020-64200-3 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wu, Long Feng, Qing Ai, Mei-Lin Deng, Song-yun Liu, Zhi-Yong Huang, Li Ai, Yu-Hang Zhang, Lina The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy |
title | The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy |
title_full | The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy |
title_fullStr | The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy |
title_full_unstemmed | The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy |
title_short | The dynamic change of serum S100B levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy |
title_sort | dynamic change of serum s100b levels from day 1 to day 3 is more associated with sepsis-associated encephalopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7206038/ https://www.ncbi.nlm.nih.gov/pubmed/32382007 http://dx.doi.org/10.1038/s41598-020-64200-3 |
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