Utility of serum macrophage migration inhibitory factor as a potential biomarker for detection of cerebrocardiac syndrome following severe traumatic brain injury

•Serum macrophage migration inhibitory factor levels are raised after brain trauma.•Serum macrophage migration inhibitory factor levels are correlated with clinical severity following brain trauma.•Serum macrophage migration inhibitory factor appears as an independent predictor for cerebrocardiac sy...

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Published inClinica chimica acta Vol. 512; pp. 179 - 184
Main Authors Dai, Jun-Xia, Lin, Qun, Ba, Hua-Jun, Ye, Liang-Zhi, Li, Zhi-Wei, Cai, Jian-Yong
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.01.2021
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Abstract •Serum macrophage migration inhibitory factor levels are raised after brain trauma.•Serum macrophage migration inhibitory factor levels are correlated with clinical severity following brain trauma.•Serum macrophage migration inhibitory factor appears as an independent predictor for cerebrocardiac syndrome. Cerebrocardiac syndrome (CCS) is a common complication after severe traumatic brain injury (sTBI) and its occurrence obviously increases the risk of a poor outcome. Macrophage migration inhibitory factor (MIF) acts as an inflammatory cytokine and its circulating concentration are related to acute heart and brain injury. The aim of this study was to examine the association of serum concentration of MIF with posttraumatic CCS. From January 2016 to February 2019, 116 sTBI patients and 116 healthy controls with similar age and gender percentage were recruited. Relationship between serum MIF concentration and CCS was assessed using multivariate analysis. Serum MIF concentration of patients were significantly higher than those among controls. Serum MIF concentration were intimately correlated with Glasgow coma scale scores (t = -5.553, P < 0.001) and serum C-reactive protein concentration (t = 5.320, P < 0.001) in a multivariate linear regression model. 61 patients (52.6%) displayed CCS. Under ROC curve analylsis, there was a strong discriminatory ability for CCS regarding serum MIF concentration (area under curve, 0.834; 95% confidence interval, 0.754–0.897). Serum MIF concentration were highly associated with CCS independent of other confounding factors (odds ratio, 5.608; 95% CI: 1.896–16.587). Increased MIF in serum may be a useful biomarker for early detection of CCS after head trauma.
AbstractList Cerebrocardiac syndrome (CCS) is a common complication after severe traumatic brain injury (sTBI) and its occurrence obviously increases the risk of a poor outcome. Macrophage migration inhibitory factor (MIF) acts as an inflammatory cytokine and its circulating concentration are related to acute heart and brain injury. The aim of this study was to examine the association of serum concentration of MIF with posttraumatic CCS. From January 2016 to February 2019, 116 sTBI patients and 116 healthy controls with similar age and gender percentage were recruited. Relationship between serum MIF concentration and CCS was assessed using multivariate analysis. Serum MIF concentration of patients were significantly higher than those among controls. Serum MIF concentration were intimately correlated with Glasgow coma scale scores (t = -5.553, P < 0.001) and serum C-reactive protein concentration (t = 5.320, P < 0.001) in a multivariate linear regression model. 61 patients (52.6%) displayed CCS. Under ROC curve analylsis, there was a strong discriminatory ability for CCS regarding serum MIF concentration (area under curve, 0.834; 95% confidence interval, 0.754-0.897). Serum MIF concentration were highly associated with CCS independent of other confounding factors (odds ratio, 5.608; 95% CI: 1.896-16.587). Increased MIF in serum may be a useful biomarker for early detection of CCS after head trauma.
BACKGROUNDCerebrocardiac syndrome (CCS) is a common complication after severe traumatic brain injury (sTBI) and its occurrence obviously increases the risk of a poor outcome. Macrophage migration inhibitory factor (MIF) acts as an inflammatory cytokine and its circulating concentration are related to acute heart and brain injury. The aim of this study was to examine the association of serum concentration of MIF with posttraumatic CCS. METHODSFrom January 2016 to February 2019, 116 sTBI patients and 116 healthy controls with similar age and gender percentage were recruited. Relationship between serum MIF concentration and CCS was assessed using multivariate analysis. RESULTSSerum MIF concentration of patients were significantly higher than those among controls. Serum MIF concentration were intimately correlated with Glasgow coma scale scores (t = -5.553, P < 0.001) and serum C-reactive protein concentration (t = 5.320, P < 0.001) in a multivariate linear regression model. 61 patients (52.6%) displayed CCS. Under ROC curve analylsis, there was a strong discriminatory ability for CCS regarding serum MIF concentration (area under curve, 0.834; 95% confidence interval, 0.754-0.897). Serum MIF concentration were highly associated with CCS independent of other confounding factors (odds ratio, 5.608; 95% CI: 1.896-16.587). CONCLUSIONSIncreased MIF in serum may be a useful biomarker for early detection of CCS after head trauma.
•Serum macrophage migration inhibitory factor levels are raised after brain trauma.•Serum macrophage migration inhibitory factor levels are correlated with clinical severity following brain trauma.•Serum macrophage migration inhibitory factor appears as an independent predictor for cerebrocardiac syndrome. Cerebrocardiac syndrome (CCS) is a common complication after severe traumatic brain injury (sTBI) and its occurrence obviously increases the risk of a poor outcome. Macrophage migration inhibitory factor (MIF) acts as an inflammatory cytokine and its circulating concentration are related to acute heart and brain injury. The aim of this study was to examine the association of serum concentration of MIF with posttraumatic CCS. From January 2016 to February 2019, 116 sTBI patients and 116 healthy controls with similar age and gender percentage were recruited. Relationship between serum MIF concentration and CCS was assessed using multivariate analysis. Serum MIF concentration of patients were significantly higher than those among controls. Serum MIF concentration were intimately correlated with Glasgow coma scale scores (t = -5.553, P < 0.001) and serum C-reactive protein concentration (t = 5.320, P < 0.001) in a multivariate linear regression model. 61 patients (52.6%) displayed CCS. Under ROC curve analylsis, there was a strong discriminatory ability for CCS regarding serum MIF concentration (area under curve, 0.834; 95% confidence interval, 0.754–0.897). Serum MIF concentration were highly associated with CCS independent of other confounding factors (odds ratio, 5.608; 95% CI: 1.896–16.587). Increased MIF in serum may be a useful biomarker for early detection of CCS after head trauma.
Author Dai, Jun-Xia
Ba, Hua-Jun
Li, Zhi-Wei
Ye, Liang-Zhi
Cai, Jian-Yong
Lin, Qun
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Keywords Macrophage migration inhibitory factor
CCS
Traumatic brain injury
GCS
Cerebrocardiac syndrome
Biomarkers
Inflammation
MIF
sTBI
Language English
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Snippet •Serum macrophage migration inhibitory factor levels are raised after brain trauma.•Serum macrophage migration inhibitory factor levels are correlated with...
Cerebrocardiac syndrome (CCS) is a common complication after severe traumatic brain injury (sTBI) and its occurrence obviously increases the risk of a poor...
BACKGROUNDCerebrocardiac syndrome (CCS) is a common complication after severe traumatic brain injury (sTBI) and its occurrence obviously increases the risk of...
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SubjectTerms Biomarkers
Brain Injuries, Traumatic - complications
Brain Injuries, Traumatic - diagnosis
C-Reactive Protein
Cerebrocardiac syndrome
Humans
Inflammation
Macrophage migration inhibitory factor
Macrophage Migration-Inhibitory Factors
Traumatic brain injury
Title Utility of serum macrophage migration inhibitory factor as a potential biomarker for detection of cerebrocardiac syndrome following severe traumatic brain injury
URI https://dx.doi.org/10.1016/j.cca.2020.11.007
https://www.ncbi.nlm.nih.gov/pubmed/33181151
https://search.proquest.com/docview/2460769294
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