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Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure

OBJECTIVES: The rapidly evolving organ failure and high short-run mortality of acute-on-chronic liver failure (ACLF) are inseparable from the role of systemic inflammatory response. S100A8 and S100A9 are associated with the excessive cytokine storm and play a decisive part within the process of infl...

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Autores principales: Zhang, Yao, Zhang, Xueyun, Han, Jiajia, Guo, Yifei, He, Jingjing, Yang, Feifei, Mao, Richeng, Huang, Yuxian, Zhang, Jiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352535/
https://www.ncbi.nlm.nih.gov/pubmed/37469934
http://dx.doi.org/10.1155/2023/6164611
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author Zhang, Yao
Zhang, Xueyun
Han, Jiajia
Guo, Yifei
He, Jingjing
Yang, Feifei
Mao, Richeng
Huang, Yuxian
Zhang, Jiming
author_facet Zhang, Yao
Zhang, Xueyun
Han, Jiajia
Guo, Yifei
He, Jingjing
Yang, Feifei
Mao, Richeng
Huang, Yuxian
Zhang, Jiming
author_sort Zhang, Yao
collection PubMed
description OBJECTIVES: The rapidly evolving organ failure and high short-run mortality of acute-on-chronic liver failure (ACLF) are inseparable from the role of systemic inflammatory response. S100A8 and S100A9 are associated with the excessive cytokine storm and play a decisive part within the process of inflammation. We aimed to clarify the role of them in predicting prognosis of hepatitis B virus-related ACLF (HBV-ACLF). METHODS: S100A8 and S100A9 levels were analyzed in plasma of 187 transplant-free HBV-ACLF patients, 28 healthy controls and 40 chronic hepatitis B (CHB) patients. S100A8 and S100A9 mRNAs were checked in liver samples from 32 HBV-ACLF patients with liver transplantation, 19 patients undergoing surgery for hepatic hemangioma and 10 CHB patients with needle biopsy. RESULTS: The plasma levels of the S100A8 and S100A9 were higher in HBV-ACLF patients than in CHB patients (S100A8 : P < 0.001 and S100A9 : P < 0.001) and healthy controls (S100A8 : P < 0.001 and S100A9 : P < 0.001), and similar results were obtained for mRNA expression. Moreover, both proteins were related to ACLF grade, different types of organ failure, and infection, and they correlated with other prognostic scoring systems. S100A8 and S100A9 can dependently predict 28/90-day mortality (28-day: S100A8: hazard ratio (HR): 1.027; 95% confidence interval (CI): 1.007–1.048; P=0.026, S100A9 : HR: 1.009; 95% CI: 1.001–1.017; P=0.007, 90-day: S100A8 : HR: 1.023; 95% CI: 1.011–1.035; P=0.004, S100A9 : HR: 1.008; 95% CI: 1.004–1.012; and P < 0.001). Among all of the scoring systems, the combined scoring model (S100A8 and S100A9 jointly with the Chronic Liver Failure-Consortium Organ Failure score (CLIF-C OFs)) displayed the highest area under the receiver operating curve (0.923 (95% CI, 0.887–0.961)) in the prediction of 90-day mortality. CONCLUSIONS: S100A8 and S100A9 are promising biomarkers for the analysis of risk stratification and prognosis in ACLF patients. In addition, combining them with the CLIF-C OFs may better predict the prognosis of ACLF.
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spelling pubmed-103525352023-07-19 Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure Zhang, Yao Zhang, Xueyun Han, Jiajia Guo, Yifei He, Jingjing Yang, Feifei Mao, Richeng Huang, Yuxian Zhang, Jiming Can J Gastroenterol Hepatol Research Article OBJECTIVES: The rapidly evolving organ failure and high short-run mortality of acute-on-chronic liver failure (ACLF) are inseparable from the role of systemic inflammatory response. S100A8 and S100A9 are associated with the excessive cytokine storm and play a decisive part within the process of inflammation. We aimed to clarify the role of them in predicting prognosis of hepatitis B virus-related ACLF (HBV-ACLF). METHODS: S100A8 and S100A9 levels were analyzed in plasma of 187 transplant-free HBV-ACLF patients, 28 healthy controls and 40 chronic hepatitis B (CHB) patients. S100A8 and S100A9 mRNAs were checked in liver samples from 32 HBV-ACLF patients with liver transplantation, 19 patients undergoing surgery for hepatic hemangioma and 10 CHB patients with needle biopsy. RESULTS: The plasma levels of the S100A8 and S100A9 were higher in HBV-ACLF patients than in CHB patients (S100A8 : P < 0.001 and S100A9 : P < 0.001) and healthy controls (S100A8 : P < 0.001 and S100A9 : P < 0.001), and similar results were obtained for mRNA expression. Moreover, both proteins were related to ACLF grade, different types of organ failure, and infection, and they correlated with other prognostic scoring systems. S100A8 and S100A9 can dependently predict 28/90-day mortality (28-day: S100A8: hazard ratio (HR): 1.027; 95% confidence interval (CI): 1.007–1.048; P=0.026, S100A9 : HR: 1.009; 95% CI: 1.001–1.017; P=0.007, 90-day: S100A8 : HR: 1.023; 95% CI: 1.011–1.035; P=0.004, S100A9 : HR: 1.008; 95% CI: 1.004–1.012; and P < 0.001). Among all of the scoring systems, the combined scoring model (S100A8 and S100A9 jointly with the Chronic Liver Failure-Consortium Organ Failure score (CLIF-C OFs)) displayed the highest area under the receiver operating curve (0.923 (95% CI, 0.887–0.961)) in the prediction of 90-day mortality. CONCLUSIONS: S100A8 and S100A9 are promising biomarkers for the analysis of risk stratification and prognosis in ACLF patients. In addition, combining them with the CLIF-C OFs may better predict the prognosis of ACLF. Hindawi 2023-07-10 /pmc/articles/PMC10352535/ /pubmed/37469934 http://dx.doi.org/10.1155/2023/6164611 Text en Copyright © 2023 Yao Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Yao
Zhang, Xueyun
Han, Jiajia
Guo, Yifei
He, Jingjing
Yang, Feifei
Mao, Richeng
Huang, Yuxian
Zhang, Jiming
Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure
title Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure
title_full Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure
title_fullStr Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure
title_full_unstemmed Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure
title_short Plasma S100A8 and S100A9 Are Strong Prognostic Factors for Hepatitis B Virus-Related Acute-on-Chronic Liver Failure
title_sort plasma s100a8 and s100a9 are strong prognostic factors for hepatitis b virus-related acute-on-chronic liver failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352535/
https://www.ncbi.nlm.nih.gov/pubmed/37469934
http://dx.doi.org/10.1155/2023/6164611
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