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High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure
BACKGROUND: Patients with hepatitis B virus-associated acute-on-chronic liver failure (HBV-ACLF) present a complex and poor prognosis. Systemic inflammation plays an important role in its pathogenesis, and interleukin-6 (IL-6) as a pro-inflammatory cytokine is related with severe liver impairment an...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438191/ https://www.ncbi.nlm.nih.gov/pubmed/32874059 http://dx.doi.org/10.3748/wjg.v26.i30.4479 |
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author | Zhou, Chao Zhang, Ning He, Ting-Ting Wang, Yao Wang, Li-Fu Sun, Yong-Qiang Jing, Jing Zhang, Jing-Jing Fu, Shuang-Nan Wang, Xuan Liang, Xiao-Xiao Li, Xin Gong, Man Li, Jun |
author_facet | Zhou, Chao Zhang, Ning He, Ting-Ting Wang, Yao Wang, Li-Fu Sun, Yong-Qiang Jing, Jing Zhang, Jing-Jing Fu, Shuang-Nan Wang, Xuan Liang, Xiao-Xiao Li, Xin Gong, Man Li, Jun |
author_sort | Zhou, Chao |
collection | PubMed |
description | BACKGROUND: Patients with hepatitis B virus-associated acute-on-chronic liver failure (HBV-ACLF) present a complex and poor prognosis. Systemic inflammation plays an important role in its pathogenesis, and interleukin-6 (IL-6) as a pro-inflammatory cytokine is related with severe liver impairment and also plays a role in promoting liver regeneration. Whether serum IL-6 influences HBV-ACLF prognosis has not been studied. AIM: To determine the impact of serum IL-6 on outcome of patients with HBV-ACLF. METHODS: We performed a retrospective study of 412 HBV-ACLF patients. The findings were analyzed with regard to mortality and the serum IL-6 level at baseline, as well as dynamic changes of serum IL-6 within 4 wk. RESULTS: The serum IL-6 level was associated with mortality. Within 4 wk, deceased patients had significantly higher levels of IL-6 at baseline than surviving patients [17.9 (7.3-57.6) vs 10.4 (4.7-22.3), P = 0.011]. Patients with high IL-6 levels (> 11.8 pg/mL) had a higher mortality within 4 wk than those with low IL-6 levels (≤ 11.8 pg/mL) (24.2% vs 13.2%, P = 0.004). The odds ratios calculated using univariate and multivariate logistic regression were 2.10 (95% confidence interval [CI]: 1.26-3.51, P = 0.005) and 2.11 (95%CI: 1.15-3.90, P = 0.017), respectively. The mortality between weeks 5 and 8 in patients with high IL-6 levels at 4 wk was 15.0%, which was significantly higher than the 6.6% mortality rate in patients with low IL-6 levels at 4 wk (hazard ratio = 2.39, 95%CI: 1.05-5.41, P = 0.037). The mortality was 5.0% in patients with high IL-6 levels at baseline and low IL-6 levels at 4 wk, 7.5% in patients with low IL-6 levels both at baseline and at 4 wk, 11.5% in patients with low IL-6 levels at baseline and high IL-6 levels at 4 wk, and 16.7% in patients with high IL-6 levels both at baseline and at 4 wk. The increasing trend of the mortality rate with the dynamic changes of IL-6 was significant (P for trend = 0.023). CONCLUSION: A high level of serum IL-6 is an independent risk factor for mortality in patients with HBV-ACLF. Furthermore, a sustained high level or dynamic elevated level of serum IL-6 indicates a higher mortality. |
format | Online Article Text |
id | pubmed-7438191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-74381912020-08-31 High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure Zhou, Chao Zhang, Ning He, Ting-Ting Wang, Yao Wang, Li-Fu Sun, Yong-Qiang Jing, Jing Zhang, Jing-Jing Fu, Shuang-Nan Wang, Xuan Liang, Xiao-Xiao Li, Xin Gong, Man Li, Jun World J Gastroenterol Retrospective Study BACKGROUND: Patients with hepatitis B virus-associated acute-on-chronic liver failure (HBV-ACLF) present a complex and poor prognosis. Systemic inflammation plays an important role in its pathogenesis, and interleukin-6 (IL-6) as a pro-inflammatory cytokine is related with severe liver impairment and also plays a role in promoting liver regeneration. Whether serum IL-6 influences HBV-ACLF prognosis has not been studied. AIM: To determine the impact of serum IL-6 on outcome of patients with HBV-ACLF. METHODS: We performed a retrospective study of 412 HBV-ACLF patients. The findings were analyzed with regard to mortality and the serum IL-6 level at baseline, as well as dynamic changes of serum IL-6 within 4 wk. RESULTS: The serum IL-6 level was associated with mortality. Within 4 wk, deceased patients had significantly higher levels of IL-6 at baseline than surviving patients [17.9 (7.3-57.6) vs 10.4 (4.7-22.3), P = 0.011]. Patients with high IL-6 levels (> 11.8 pg/mL) had a higher mortality within 4 wk than those with low IL-6 levels (≤ 11.8 pg/mL) (24.2% vs 13.2%, P = 0.004). The odds ratios calculated using univariate and multivariate logistic regression were 2.10 (95% confidence interval [CI]: 1.26-3.51, P = 0.005) and 2.11 (95%CI: 1.15-3.90, P = 0.017), respectively. The mortality between weeks 5 and 8 in patients with high IL-6 levels at 4 wk was 15.0%, which was significantly higher than the 6.6% mortality rate in patients with low IL-6 levels at 4 wk (hazard ratio = 2.39, 95%CI: 1.05-5.41, P = 0.037). The mortality was 5.0% in patients with high IL-6 levels at baseline and low IL-6 levels at 4 wk, 7.5% in patients with low IL-6 levels both at baseline and at 4 wk, 11.5% in patients with low IL-6 levels at baseline and high IL-6 levels at 4 wk, and 16.7% in patients with high IL-6 levels both at baseline and at 4 wk. The increasing trend of the mortality rate with the dynamic changes of IL-6 was significant (P for trend = 0.023). CONCLUSION: A high level of serum IL-6 is an independent risk factor for mortality in patients with HBV-ACLF. Furthermore, a sustained high level or dynamic elevated level of serum IL-6 indicates a higher mortality. Baishideng Publishing Group Inc 2020-08-14 2020-08-14 /pmc/articles/PMC7438191/ /pubmed/32874059 http://dx.doi.org/10.3748/wjg.v26.i30.4479 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Retrospective Study Zhou, Chao Zhang, Ning He, Ting-Ting Wang, Yao Wang, Li-Fu Sun, Yong-Qiang Jing, Jing Zhang, Jing-Jing Fu, Shuang-Nan Wang, Xuan Liang, Xiao-Xiao Li, Xin Gong, Man Li, Jun High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure |
title | High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure |
title_full | High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure |
title_fullStr | High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure |
title_full_unstemmed | High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure |
title_short | High levels of serum interleukin-6 increase mortality of hepatitis B virus-associated acute-on-chronic liver failure |
title_sort | high levels of serum interleukin-6 increase mortality of hepatitis b virus-associated acute-on-chronic liver failure |
topic | Retrospective Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438191/ https://www.ncbi.nlm.nih.gov/pubmed/32874059 http://dx.doi.org/10.3748/wjg.v26.i30.4479 |
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