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

感染性休克 败血症 医学 血小板生成素 免疫学 炎症 休克(循环) 拯救脓毒症运动 内科学 生物 严重败血症 造血 干细胞 遗传学
作者
Chang Liu,Dennis Görlich,Clifford A. Lowell,Joseph E. Italiano,Jan Rossaint,Markus Bender,Alexander Zarbock,Andreas Margraf
出处
期刊:Clinical Chemistry and Laboratory Medicine [De Gruyter]
卷期号:62 (5): 999-1010
标识
DOI:10.1515/cclm-2023-0792
摘要

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.
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