High levels of serum macrophage migration inhibitory factor and interleukin 10 are associated with a rapidly fatal outcome in patients with severe sepsis

The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early phase of sepsis and rapidly fatal outcome. One hundred and fifty-three adult subjects with the main diagnosis of severe sepsis (including se...

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Published inInternational journal of infectious diseases Vol. 20; pp. 13 - 17
Main Authors Chuang, Tzu-Yi, Chang, Hou-Tai, Chung, Kuei-Pin, Cheng, Hui-Shan, Liu, Chung-Yang, Liu, Yen-Chun, Huang, Hsiu-Han, Chou, Ting-Chen, Chang, Bei-Ling, Lee, Meng-Rui, Lin, Chou-Jui, Lee, Shih-Wei, Yu, Chong-Jen, Hsueh, Po-Ren
Format Journal Article
LanguageEnglish
Published Canada Elsevier Ltd 01.03.2014
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ISSN1201-9712
1878-3511
1878-3511
DOI10.1016/j.ijid.2013.12.006

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Abstract The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early phase of sepsis and rapidly fatal outcome. One hundred and fifty-three adult subjects with the main diagnosis of severe sepsis (including septic shock) admitted directly from the emergency department of two tertiary medical centers and one regional teaching hospital between January 2009 and December 2011, were included prospectively. MIF and IL-10 levels were measured and outcomes were analyzed by Cox regression analysis according to the following outcomes: rapidly fatal outcome (RFO, death within 48h), late fatal outcome (LFO, death between 48h and 28 days), and survival at 28 days. Among the three outcome groups, IL-10 levels were significantly higher in the RFO group (p < 0.001) and no significant differences were seen between the LFO and survivor groups. After Cox regression analysis, each incremental elevation of 1000 pg/ml in both IL-10 and MIF was independently associated with RFO in patients with severe sepsis. Each incremental elevation of 1000 pg/ml in IL-10 increased the RFO risk by a factor of 1.312 (95% confidence interval 1.094–1.575; p=0.003); this was the most significant factor leading to RFO in patients with severe sepsis. Patients with RFO exhibited simultaneously high MIF and IL-10 levels in the early phase of severe sepsis. Incremental increases in both IL-10 and MIF levels were associated with RFO in this patient group, and of the two, IL-10 was the most significant factor linked to RFO.
AbstractList Summary Objectives The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early phase of sepsis and rapidly fatal outcome. Methods One hundred and fifty-three adult subjects with the main diagnosis of severe sepsis (including septic shock) admitted directly from the emergency department of two tertiary medical centers and one regional teaching hospital between January 2009 and December 2011, were included prospectively. MIF and IL-10 levels were measured and outcomes were analyzed by Cox regression analysis according to the following outcomes: rapidly fatal outcome (RFO, death within 48 h), late fatal outcome (LFO, death between 48 h and 28 days), and survival at 28 days. Results Among the three outcome groups, IL-10 levels were significantly higher in the RFO group ( p < 0.001) and no significant differences were seen between the LFO and survivor groups. After Cox regression analysis, each incremental elevation of 1000 pg/ml in both IL-10 and MIF was independently associated with RFO in patients with severe sepsis. Each incremental elevation of 1000 pg/ml in IL-10 increased the RFO risk by a factor of 1.312 (95% confidence interval 1.094–1.575; p = 0.003); this was the most significant factor leading to RFO in patients with severe sepsis. Conclusions Patients with RFO exhibited simultaneously high MIF and IL-10 levels in the early phase of severe sepsis. Incremental increases in both IL-10 and MIF levels were associated with RFO in this patient group, and of the two, IL-10 was the most significant factor linked to RFO.
The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early phase of sepsis and rapidly fatal outcome. One hundred and fifty-three adult subjects with the main diagnosis of severe sepsis (including septic shock) admitted directly from the emergency department of two tertiary medical centers and one regional teaching hospital between January 2009 and December 2011, were included prospectively. MIF and IL-10 levels were measured and outcomes were analyzed by Cox regression analysis according to the following outcomes: rapidly fatal outcome (RFO, death within 48h), late fatal outcome (LFO, death between 48h and 28 days), and survival at 28 days. Among the three outcome groups, IL-10 levels were significantly higher in the RFO group (p < 0.001) and no significant differences were seen between the LFO and survivor groups. After Cox regression analysis, each incremental elevation of 1000 pg/ml in both IL-10 and MIF was independently associated with RFO in patients with severe sepsis. Each incremental elevation of 1000 pg/ml in IL-10 increased the RFO risk by a factor of 1.312 (95% confidence interval 1.094–1.575; p=0.003); this was the most significant factor leading to RFO in patients with severe sepsis. Patients with RFO exhibited simultaneously high MIF and IL-10 levels in the early phase of severe sepsis. Incremental increases in both IL-10 and MIF levels were associated with RFO in this patient group, and of the two, IL-10 was the most significant factor linked to RFO.
The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early phase of sepsis and rapidly fatal outcome. One hundred and fifty-three adult subjects with the main diagnosis of severe sepsis (including septic shock) admitted directly from the emergency department of two tertiary medical centers and one regional teaching hospital between January 2009 and December 2011, were included prospectively. MIF and IL-10 levels were measured and outcomes were analyzed by Cox regression analysis according to the following outcomes: rapidly fatal outcome (RFO, death within 48 h), late fatal outcome (LFO, death between 48 h and 28 days), and survival at 28 days. Among the three outcome groups, IL-10 levels were significantly higher in the RFO group (p < 0.001) and no significant differences were seen between the LFO and survivor groups. After Cox regression analysis, each incremental elevation of 1000 pg/ml in both IL-10 and MIF was independently associated with RFO in patients with severe sepsis. Each incremental elevation of 1000 pg/ml in IL-10 increased the RFO risk by a factor of 1.312 (95% confidence interval 1.094-1.575; p=0.003); this was the most significant factor leading to RFO in patients with severe sepsis. Patients with RFO exhibited simultaneously high MIF and IL-10 levels in the early phase of severe sepsis. Incremental increases in both IL-10 and MIF levels were associated with RFO in this patient group, and of the two, IL-10 was the most significant factor linked to RFO.
The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early phase of sepsis and rapidly fatal outcome.OBJECTIVESThe aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early phase of sepsis and rapidly fatal outcome.One hundred and fifty-three adult subjects with the main diagnosis of severe sepsis (including septic shock) admitted directly from the emergency department of two tertiary medical centers and one regional teaching hospital between January 2009 and December 2011, were included prospectively. MIF and IL-10 levels were measured and outcomes were analyzed by Cox regression analysis according to the following outcomes: rapidly fatal outcome (RFO, death within 48 h), late fatal outcome (LFO, death between 48 h and 28 days), and survival at 28 days.METHODSOne hundred and fifty-three adult subjects with the main diagnosis of severe sepsis (including septic shock) admitted directly from the emergency department of two tertiary medical centers and one regional teaching hospital between January 2009 and December 2011, were included prospectively. MIF and IL-10 levels were measured and outcomes were analyzed by Cox regression analysis according to the following outcomes: rapidly fatal outcome (RFO, death within 48 h), late fatal outcome (LFO, death between 48 h and 28 days), and survival at 28 days.Among the three outcome groups, IL-10 levels were significantly higher in the RFO group (p < 0.001) and no significant differences were seen between the LFO and survivor groups. After Cox regression analysis, each incremental elevation of 1000 pg/ml in both IL-10 and MIF was independently associated with RFO in patients with severe sepsis. Each incremental elevation of 1000 pg/ml in IL-10 increased the RFO risk by a factor of 1.312 (95% confidence interval 1.094-1.575; p=0.003); this was the most significant factor leading to RFO in patients with severe sepsis.RESULTSAmong the three outcome groups, IL-10 levels were significantly higher in the RFO group (p < 0.001) and no significant differences were seen between the LFO and survivor groups. After Cox regression analysis, each incremental elevation of 1000 pg/ml in both IL-10 and MIF was independently associated with RFO in patients with severe sepsis. Each incremental elevation of 1000 pg/ml in IL-10 increased the RFO risk by a factor of 1.312 (95% confidence interval 1.094-1.575; p=0.003); this was the most significant factor leading to RFO in patients with severe sepsis.Patients with RFO exhibited simultaneously high MIF and IL-10 levels in the early phase of severe sepsis. Incremental increases in both IL-10 and MIF levels were associated with RFO in this patient group, and of the two, IL-10 was the most significant factor linked to RFO.CONCLUSIONSPatients with RFO exhibited simultaneously high MIF and IL-10 levels in the early phase of severe sepsis. Incremental increases in both IL-10 and MIF levels were associated with RFO in this patient group, and of the two, IL-10 was the most significant factor linked to RFO.
Author Lee, Meng-Rui
Chung, Kuei-Pin
Chang, Bei-Ling
Hsueh, Po-Ren
Lee, Shih-Wei
Liu, Chung-Yang
Chou, Ting-Chen
Huang, Hsiu-Han
Chang, Hou-Tai
Liu, Yen-Chun
Chuang, Tzu-Yi
Cheng, Hui-Shan
Lin, Chou-Jui
Yu, Chong-Jen
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  organization: Department of Critical Care Medicine, Far Eastern Memorial Hospital, Taipei, Taiwan
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  fullname: Chung, Kuei-Pin
  organization: Departments of Laboratory Medicine and Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, No. 7, Chung-Shan S. Rd., Taipei 100, Taiwan
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  givenname: Hui-Shan
  surname: Cheng
  fullname: Cheng, Hui-Shan
  organization: Departments of Laboratory Medicine and Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, No. 7, Chung-Shan S. Rd., Taipei 100, Taiwan
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  givenname: Chung-Yang
  surname: Liu
  fullname: Liu, Chung-Yang
  organization: Department of Communications Management, Ming Chuan University, Taipei, Taiwan
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  surname: Liu
  fullname: Liu, Yen-Chun
  organization: Center of Tuberculosis Prevention, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan
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  fullname: Huang, Hsiu-Han
  organization: Center of Tuberculosis Prevention, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan
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  givenname: Ting-Chen
  surname: Chou
  fullname: Chou, Ting-Chen
  organization: Center of Tuberculosis Prevention, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan
– sequence: 9
  givenname: Bei-Ling
  surname: Chang
  fullname: Chang, Bei-Ling
  organization: Department of Laboratory Medicine, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan
– sequence: 10
  givenname: Meng-Rui
  surname: Lee
  fullname: Lee, Meng-Rui
  organization: Department of Internal Medicine, National Taiwan University Hospital Hsin-Chu Branch, National Taiwan University College of Medicine, Hsin-Chu, Taiwan
– sequence: 11
  givenname: Chou-Jui
  surname: Lin
  fullname: Lin, Chou-Jui
  organization: Department of Internal Medicine, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan
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  surname: Lee
  fullname: Lee, Shih-Wei
  organization: Department of Internal Medicine, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan
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  givenname: Chong-Jen
  surname: Yu
  fullname: Yu, Chong-Jen
  organization: Department of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan
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  givenname: Po-Ren
  surname: Hsueh
  fullname: Hsueh, Po-Ren
  email: hsporen@ntu.edu.tw
  organization: Departments of Laboratory Medicine and Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, No. 7, Chung-Shan S. Rd., Taipei 100, Taiwan
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Keywords Macrophage migration inhibitory factor
Intensive care units
Rapidly fatal outcome
Severe sepsis
Interleukin 10
Language English
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Snippet The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10) levels in the early...
Summary Objectives The aim of this study was to delineate the association between high macrophage migration inhibitory factor (MIF) and interleukin 10 (IL-10)...
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SubjectTerms Adult
Aged
Aged, 80 and over
Female
Humans
Infectious Disease
Intensive care units
Interleukin 10
Interleukin-10 - blood
Macrophage migration inhibitory factor
Macrophage Migration-Inhibitory Factors - blood
Male
Middle Aged
Proportional Hazards Models
Prospective Studies
Pulmonary/Respiratory
Rapidly fatal outcome
Sepsis - blood
Sepsis - diagnosis
Sepsis - mortality
Severe sepsis
Shock, Septic - mortality
Title High levels of serum macrophage migration inhibitory factor and interleukin 10 are associated with a rapidly fatal outcome in patients with severe sepsis
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https://www.clinicalkey.es/playcontent/1-s2.0-S1201971214000204
https://dx.doi.org/10.1016/j.ijid.2013.12.006
https://www.ncbi.nlm.nih.gov/pubmed/24445225
https://www.proquest.com/docview/1505254265
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