7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Immunological risk factors for sepsis-associated delirium and mortality in ICU patients

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          A major challenge in intervention of critical patients, especially sepsis-associated delirium (SAD) intervention, is the lack of predictive risk factors. As sepsis and SAD are heavily entangled with inflammatory and immunological processes, to identify the risk factors of SAD and mortality in the intensive care unit (ICU) and determine the underlying molecular mechanisms, the peripheral immune profiles of patients in the ICU were characterized.

          Methods

          This study contains a cohort of 52 critical patients who were admitted to the ICU of the First Affiliated Hospital of Jinan University. Comorbidity, including sepsis and SAD, of this cohort was diagnosed and recorded. Furthermore, peripheral blood samples were collected on days 1, 3, and 5 of admission for peripheral immune profiling with blood routine examination, flow cytometry, ELISA, RNA-seq, and qPCR.

          Results

          The patients with SAD had higher mortality during ICU admission and within 28 days of discharge. Compared with survivors, nonsurvivors had higher neutrophilic granulocyte percentage, higher CRP concentration, lower monocyte count, lower monocyte percentage, lower C3 complement level, higher CD14 loCD16 + monocytes percentage, and higher levels of IL-6 and TNFα. The CD14 hiCD16 - monocyte percentage manifested favorable prediction values for the occurrence of SAD. Differentially expressed genes between the nonsurvival and survival groups were mainly associated with immune response and metabolism process. The longitudinal expression pattern of SLC2A1 and STIMATE were different between nonsurvivors and survivors, which were validated by qPCR.

          Conclusions

          Nonsurvival critical patients have a distinct immune profile when compared with survival patients. CD14 hiCD16 - monocyte prevalence and expression levels of SLC2A1 and STIMATE may be predictors of SAD and 28-day mortality in ICU patients.

          Related collections

          Most cited references38

          • Record: found
          • Abstract: found
          • Article: found

          The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3).

          Definitions of sepsis and septic shock were last revised in 2001. Considerable advances have since been made into the pathobiology (changes in organ function, morphology, cell biology, biochemistry, immunology, and circulation), management, and epidemiology of sepsis, suggesting the need for reexamination.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Clinical Practice Guidelines for the Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICU

            To update and expand the 2013 Clinical Practice Guidelines for the Management of Pain, Agitation, and Delirium in Adult Patients in the ICU.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Severe Sepsis and Septic Shock

                Bookmark

                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                20 September 2022
                2022
                : 13
                : 940779
                Affiliations
                [1] 1 Department of Microbiology and Immunology, School of Medicine, Jinan University , Guangzhou, China
                [2] 2 Institute of Geriatric Immunology, School of Medicine, Jinan University , Guangzhou, China
                [3] 3 Guangdong-Hong Kong-Macau Great Bay Area Geroscience Joint Laboratory, Jinan University , Guangzhou, China
                [4] 4 Department of Systems Biomedical Sciences, School of Medicine, Jinan University , Guangzhou, China
                [5] 5 National Health Commission (NHC) Key Laboratory of Male Reproduction and Genetics , Guangzhou, China
                [6] 6 Department of Central Laboratory, Guangdong Provincial Reproductive Science Institute (Guangdong Provincial Fertility Hospital) , Guangzhou, China
                [7] 7 Department of Sonograph, The First Affiliated Hospital, Jinan University , Guangzhou, China
                [8] 8 Department of Critical Care Medicine, The First Affiliated Hospital, Jinan University , Guangzhou, China
                Author notes

                Edited by: Steven O'Reilly, STipe Therapeutics, Denmark

                Reviewed by: Roshni Roy, National Institute on Aging (NIH), United States; Paula Trzepacz, Indiana University Bloomington, United States

                *Correspondence: Zhigang Wang, drwangzg@ 123456sina.com ; Guobing Chen, guobingchen@ 123456jnu.edu.cn ; Oscar Junhong Luo, luojh@ 123456jnu.edu.cn

                †These authors have contributed equally to this work and share first authorship

                This article was submitted to Systems Immunology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2022.940779
                9531264
                36203605
                f43455e9-b3e3-4b8a-9dbc-0df287546966
                Copyright © 2022 Lei, Ren, Su, Zheng, Gao, Xu, Deng, Xiao, Sheng, Cheng, Ma, Liu, Wang, Luo, Chen and Wang

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 10 May 2022
                : 22 August 2022
                Page count
                Figures: 4, Tables: 2, Equations: 0, References: 38, Pages: 13, Words: 6377
                Funding
                Funded by: National Key Research and Development Program of China , doi 10.13039/501100012166;
                Award ID: 2018YFC2002003
                Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
                Award ID: U1801285, 81971301, 32050410285
                Funded by: Basic and Applied Basic Research Foundation of Guangdong Province , doi 10.13039/501100021171;
                Award ID: 2020A1515010538
                Categories
                Immunology
                Original Research

                Immunology
                icu,sepsis-associated delirium,immune profile,mortality,gene expression,monocyte
                Immunology
                icu, sepsis-associated delirium, immune profile, mortality, gene expression, monocyte

                Comments

                Comment on this article