Startseite Thrombopoietin levels in sepsis and septic shock – a systematic review and meta-analysis
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Thrombopoietin levels in sepsis and septic shock – a systematic review and meta-analysis

  • Chang Liu , Dennis Görlich , Clifford A. Lowell , Joseph E. Italiano , Jan Rossaint , Markus Bender , Alexander Zarbock und Andreas Margraf ORCID logo EMAIL logo
Veröffentlicht/Copyright: 1. Dezember 2023
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Abstract

Objectives

Sepsis is a life-threatening condition implicating an inadequate activation of the immune system. Platelets act as modulators and contributors to immune processes. Indeed, altered platelet turnover, thrombotic events, and changes in thrombopoietin levels in systemic inflammation have been reported, but thrombopoietin-levels in sepsis and septic-shock have not yet been systematically evaluated. We therefore performed a meta-analysis of thrombopoietin (TPO)-levels in patients with sepsis.

Methods

Two independent reviewers screened records and full-text articles for inclusion. Scientific databases were searched for studies examining thrombopoietin levels in adult sepsis and septic-shock patients until August 1st 2022.

Results

Of 95 items screened, six studies met the inclusion criteria, including 598 subjects. Both sepsis and severe sepsis were associated with increased levels of thrombopoietin (sepsis vs. control: standardized mean difference 3.06, 95 % CI 1.35–4.77; Z=3.50, p=0.0005) (sepsis vs. severe sepsis: standardized mean difference −1.67, 95 % CI −2.46 to −0.88; Z=4.14, p<0.0001). TPO-levels did not show significant differences between severe sepsis and septic shock patients but differed between sepsis and inflammation-associated non-septic controls. Overall, high heterogeneity and low sample size could be noted.

Conclusions

Concluding, increased levels of thrombopoietin appear to be present both in sepsis and severe sepsis with high heterogeneity but thrombopoietin does not allow to differentiate between severe sepsis and septic-shock. TPO may potentially serve to differentiate sepsis from non-septic trauma and/or tissue damage related (systemic) inflammation. Usage of different assays and high heterogeneity demand standardization of methods and further large multicenter trials.


Corresponding author: Dr. med. Andreas Margraf, Department of Anesthesiology, Intensive Care and Pain Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, Münster, Germany; and Centre for Biochemical Pharmacology, William Harvey Research Institute, Faculty of Medicine and Dentistry, Queen Mary University of London, EC1M 6BQ London, UK, Phone: (+49)251/83 46841, Fax: (+49)251/83 48667, E-mail:

Award Identifier / Grant number: KFO 342, MA9604/1-1, MA9604/2-1, RO4537/4-1, RO4537/5-1, ZA428/18-1

Funding source: IZKF Münster

Award Identifier / Grant number: SEED 12/18

  1. Research ethics: Not applicable.

  2. Informed consent: Not applicable.

  3. Author contributions: CL, AM screened literature. CL, AM performed data assessment and calculations. DG acted as statistical consultant. CL contributed to writing the manuscript. CAL, JR, MB, JEI, DG, AZ gave crucial input and contributed to writing the manuscript. AM conceived of and supervised the study, wrote the manuscript. All authors revised and approved the final version of the manuscript, accept responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: The authors state no conflict of interest.

  5. Research funding: This study was supported by the Interdisciplinary Center for Clinical Research (IZKF, SEED 12/18 to A.M.) and the DFG (KFO342, RO4537/4-1 and RO4537/5-1 to J.R., ZA428/18-1 to A.Z. and MA9604/1-1 and MA9604/2-1 to A.M.). The funding organizations played no role in the study design, in the collection, analysis, and interpretation of data, in the writing of the report, or in the decision to submit the report for publication.

  6. Data availability: Data generated or analysed during this study are included in this published article and its supplementary information files (compare Supplementary File 1: Summary of Data Table).

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Supplementary Material

This article contains supplementary material (https://doi.org/10.1515/cclm-2023-0792).


Received: 2023-07-25
Accepted: 2023-11-17
Published Online: 2023-12-01
Published in Print: 2024-04-25

© 2023 Walter de Gruyter GmbH, Berlin/Boston

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