Macrophage migration inhibitory factor levels correlate with fatal outcome in sepsis
被引:145
作者:
Bozza, FA
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机构:Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
Bozza, FA
Gomes, RN
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机构:Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
Gomes, RN
Japiassú, AM
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机构:Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
Japiassú, AM
Soares, M
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机构:Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
Soares, M
Castro-Faria-Neto, HC
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机构:Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
Castro-Faria-Neto, HC
Bozza, PT
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机构:Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
Bozza, PT
Bozza, MT
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机构:Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
Bozza, MT
机构:
[1] Univ Fed Rio de Janeiro, Inst Microbiol, Dept Imunol, BR-21941590 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Hosp Univ Clementino Grafa Filho, ICU, BR-21941590 Rio De Janeiro, Brazil
[3] Hosp Espanol, ICU, Rio De Janeiro, Brazil
[4] Fundacao Oswaldo Cruz, IOC, Dept Fisiol & Farmacodinam, Lab Imunofarmacol, Rio De Janeiro, Brazil
[5] Inst Nacl Canc, ICU, Rio De Janeiro, Brazil
来源:
SHOCK
|
2004年
/
22卷
/
04期
关键词:
sepsis;
MIF;
IL-6;
cytokine;
mortality;
markers;
D O I:
10.1097/01.shk.0000140305.01641.c8
中图分类号:
R4 [临床医学];
学科分类号:
1002 ;
100602 ;
摘要:
Macrophage migration inhibitory factor (MIF) is a cytokine playing a critical role in the pathophysiology of experimental sepsis. The purpose of this study was to determine the levels of MIF and to compare those to interleukin-6 (IL-6) levels in predicting mortality among critically ill patients with sepsis. The levels of MIF and IL-6 were measured in 25 patients with septic shock, 17 patients with sepsis, and 11 healthy volunteers. The median plasma concentrations of MIF and IL-6 were significantly higher in patients with septic shock and in patients with sepsis than in healthy controls. MIF levels were significantly different between survivors and nonsurvivors, as were IL-6 levels. Discriminatory power in predicting mortality, as assessed by the areas under receiver operating characteristic curves (AUROC), was 0.793 for MIF and 0.680 for IL-6. Finally, high plasma levels of MIF (>1100 pg/mL) had a sensitivity of 100% and a specificity of 64% to identify the patients who eventually would evolve to a fatal outcome. Thus, our data suggest that an elevated MIF level in recently diagnosed septic patients appears to be an early indicator of poor outcome and a potential entry criterion for future studies with therapeutic intervention aiming at MIF neutralization.