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Clinical significance and prognosis of serum tenascin-C in patients with sepsis

BACKGROUND: Tenascin-C is a pro-inflammatory glycoprotein with various biological functions. High expression of tenascin-C is found in inflammation, tissue remodeling, and autoimmune diseases. However, its expression and clinical significance in sepsis remain unclear. This study was designed to inve...

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Autores principales: Yuan, Weifang, Zhang, Wei, Yang, Xiaofang, Zhou, Liyuan, Hanghua, Ziwei, Xu, Kailiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238343/
https://www.ncbi.nlm.nih.gov/pubmed/30442110
http://dx.doi.org/10.1186/s12871-018-0634-1
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author Yuan, Weifang
Zhang, Wei
Yang, Xiaofang
Zhou, Liyuan
Hanghua, Ziwei
Xu, Kailiang
author_facet Yuan, Weifang
Zhang, Wei
Yang, Xiaofang
Zhou, Liyuan
Hanghua, Ziwei
Xu, Kailiang
author_sort Yuan, Weifang
collection PubMed
description BACKGROUND: Tenascin-C is a pro-inflammatory glycoprotein with various biological functions. High expression of tenascin-C is found in inflammation, tissue remodeling, and autoimmune diseases. However, its expression and clinical significance in sepsis remain unclear. This study was designed to investigate the relationship between serum tenascin-C levels and disease severity and prognosis in patients with sepsis. METHODS: A total of 167 patients with sepsis admitted to the ICU were enrolled. Lood samples were collected within 24 h of admission. Serum tenascin-C levels were measured by enzyme-linked immunosorbent assay (ELISA). Follow-up was performed to observe 30-day mortality. RESULTS: Serum tenascin-C levels were significantly elevated in patients with sepsis compared with non-sepsis controls (P < 0.001). Serum tenascin-C levels were higher in nonsurvivors (58 cases) who died within 30 days (34.5%) compared to survivors (109 cases) (P < 0.001). In patients with sepsis, serum tenascin-C levels were significantly positively correlated with SOFA scores (P = 0.011), serum creatinine (P = 0.006), C-reactive protein (CRP) (P = 0.001), interleukin-6 (IL-6) (P < 0.001), and tumor necrosis factor α (TNF-α) (P = 0.026). Logistic multivariate regression models showed that serum tenascin-C levels were independent contributor of 30-day mortality. Kaplan-Meier curves showed that septic patients with high levels of serum tenascin-C (≥56.9 pg/mL) had significantly higher 30-day mortality than those with lower serum tenascin-C (< 56.9 pg/mL) (P < 0.001). CONCLUSION: Elevated serum tenascin-C was found in septic patients and associated with severity and poor prognosis.
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spelling pubmed-62383432018-11-26 Clinical significance and prognosis of serum tenascin-C in patients with sepsis Yuan, Weifang Zhang, Wei Yang, Xiaofang Zhou, Liyuan Hanghua, Ziwei Xu, Kailiang BMC Anesthesiol Research Article BACKGROUND: Tenascin-C is a pro-inflammatory glycoprotein with various biological functions. High expression of tenascin-C is found in inflammation, tissue remodeling, and autoimmune diseases. However, its expression and clinical significance in sepsis remain unclear. This study was designed to investigate the relationship between serum tenascin-C levels and disease severity and prognosis in patients with sepsis. METHODS: A total of 167 patients with sepsis admitted to the ICU were enrolled. Lood samples were collected within 24 h of admission. Serum tenascin-C levels were measured by enzyme-linked immunosorbent assay (ELISA). Follow-up was performed to observe 30-day mortality. RESULTS: Serum tenascin-C levels were significantly elevated in patients with sepsis compared with non-sepsis controls (P < 0.001). Serum tenascin-C levels were higher in nonsurvivors (58 cases) who died within 30 days (34.5%) compared to survivors (109 cases) (P < 0.001). In patients with sepsis, serum tenascin-C levels were significantly positively correlated with SOFA scores (P = 0.011), serum creatinine (P = 0.006), C-reactive protein (CRP) (P = 0.001), interleukin-6 (IL-6) (P < 0.001), and tumor necrosis factor α (TNF-α) (P = 0.026). Logistic multivariate regression models showed that serum tenascin-C levels were independent contributor of 30-day mortality. Kaplan-Meier curves showed that septic patients with high levels of serum tenascin-C (≥56.9 pg/mL) had significantly higher 30-day mortality than those with lower serum tenascin-C (< 56.9 pg/mL) (P < 0.001). CONCLUSION: Elevated serum tenascin-C was found in septic patients and associated with severity and poor prognosis. BioMed Central 2018-11-15 /pmc/articles/PMC6238343/ /pubmed/30442110 http://dx.doi.org/10.1186/s12871-018-0634-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yuan, Weifang
Zhang, Wei
Yang, Xiaofang
Zhou, Liyuan
Hanghua, Ziwei
Xu, Kailiang
Clinical significance and prognosis of serum tenascin-C in patients with sepsis
title Clinical significance and prognosis of serum tenascin-C in patients with sepsis
title_full Clinical significance and prognosis of serum tenascin-C in patients with sepsis
title_fullStr Clinical significance and prognosis of serum tenascin-C in patients with sepsis
title_full_unstemmed Clinical significance and prognosis of serum tenascin-C in patients with sepsis
title_short Clinical significance and prognosis of serum tenascin-C in patients with sepsis
title_sort clinical significance and prognosis of serum tenascin-c in patients with sepsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238343/
https://www.ncbi.nlm.nih.gov/pubmed/30442110
http://dx.doi.org/10.1186/s12871-018-0634-1
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