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 in | International journal of infectious diseases Vol. 20; pp. 13 - 17 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
01.03.2014
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ISSN | 1201-9712 1878-3511 1878-3511 |
DOI | 10.1016/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. |
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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 |
Author_xml | – sequence: 1 givenname: Tzu-Yi surname: Chuang fullname: Chuang, Tzu-Yi organization: Department of Internal Medicine, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan – sequence: 2 givenname: Hou-Tai surname: Chang fullname: Chang, Hou-Tai organization: Department of Critical Care Medicine, Far Eastern Memorial Hospital, Taipei, Taiwan – sequence: 3 givenname: Kuei-Pin surname: Chung 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 – sequence: 4 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 – sequence: 5 givenname: Chung-Yang surname: Liu fullname: Liu, Chung-Yang organization: Department of Communications Management, Ming Chuan University, Taipei, Taiwan – sequence: 6 givenname: Yen-Chun surname: Liu fullname: Liu, Yen-Chun organization: Center of Tuberculosis Prevention, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan – sequence: 7 givenname: Hsiu-Han surname: Huang fullname: Huang, Hsiu-Han organization: Center of Tuberculosis Prevention, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan – sequence: 8 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 – sequence: 12 givenname: Shih-Wei surname: Lee fullname: Lee, Shih-Wei organization: Department of Internal Medicine, Taoyuan General Hospital, Department of Health, Taoyuan, Taiwan – sequence: 13 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 – sequence: 14 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 |
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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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