Association between IL-6-174G/C Polymorphism and the Risk of Sepsis and Mortality: A Systematic Review and Meta-Analysis

被引:38
作者
Gao, Jun-wei [1 ]
Zhang, An-qiang [1 ]
Pan, Wei [1 ]
Yue, Cai-li [1 ]
Zeng, Ling [1 ]
Gu, Wei [1 ]
Jiang, Jianxin [1 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Inst Surg Res, State Key Lab Trauma Burns & Combined Injury, Chongqing 400042, Peoples R China
基金
国家杰出青年科学基金;
关键词
TNF-ALPHA POLYMORPHISMS; C-REACTIVE PROTEIN; GENETIC POLYMORPHISMS; PROMOTER POLYMORPHISM; INTERLEUKIN-6; GENE; UNITED-STATES; IL-6; VARIANTS; SEVERITY; MARKERS;
D O I
10.1371/journal.pone.0118843
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background Recent studies have reported the association between IL-6-174G/C polymorphism and sepsis. However, the results are inconclusive and conflicting. To better understand the role of IL-6-174G/C polymorphism in sepsis, we conducted a comprehensive meta-analysis. Methodology Literature search was conducted through PubMed, Embase, Web of Knowledge databases until July 29, 2013. The pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using fixed- or random-effect model based on heterogeneity test in total and subgroup analyses. Results Twenty studies on the risk of sepsis and seven studies on sepsis mortality were included. None of the results showed evidence of a significant association between IL-6-174 G/C polymorphism and sepsis risk in overall analysis or subgroup analyses based on sepsis type, ethnicity, source of control and age under any genetic model (the allele comparison, the codominant, the recessive or the dominant model). Although there was a statistically significant association between IL-6-174 G/C polymorphism and sepsis-related mortality under the recessive model, the significance did not exist after Bonferroni's correction. Conclusions Current evidence does not support a direct effect of IL-6-174 G/C polymorphism on the risk of sepsis. In addition, there was no association between IL-6-174 G/C polymorphism and sepsis mortality after Bonferroni's correction. Further analyses of gene-environment interactions and more studies based on larger sample size and homogeneous sepsis patients are required.
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页数:13
相关论文
共 40 条
[1]
Genetic polymorphisms of IL-6-174 and IL-10-1082 in full term neonates with late onset blood stream infections [J].
Abdel-Hady, Hesham ;
El-Naggar, Mohamed ;
El-Nady, Ghada ;
Badr, Rawia ;
El-Daker, Medhat .
JOURNAL OF PEDIATRIC INFECTIOUS DISEASES, 2009, 4 (04) :357-365
[2]
Mutations of genes involved in the innate immune system as predictors of sepsis in very low birth weight infants [J].
Ahrens, P ;
Kattner, E ;
Köhler, B ;
Härtel, C ;
Seidenberg, J ;
Segerer, H ;
Möller, J ;
Göpel, W .
PEDIATRIC RESEARCH, 2004, 55 (04) :652-656
[3]
Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[4]
IL-10, IL-6 and CD14 polymorphisms and sepsis outcome in ventilated very low birth weight infants [J].
Baier, R. John ;
Loggins, John ;
Yanamandra, Krishna .
BMC MEDICINE, 2006, 4 (1)
[5]
Genomic polymorphic profiles in an Irish population with meningococcaemia: is it possible to predict severity and outcome of disease? [J].
Balding, J ;
Healy, CM ;
Livingstone, WJ ;
White, B ;
Mynett-Johnson, L ;
Cafferkey, M ;
Smith, OP .
GENES AND IMMUNITY, 2003, 4 (08) :533-540
[6]
TLR4 and TNF-α polymorphisms are associated with an increased risk for severe sepsis following burn injury [J].
Barber, RC ;
Aragaki, CC ;
Rivera-Chavez, FA ;
Purdue, GF ;
Hunt, JL ;
Horton, JW .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (11) :808-U1
[7]
AMERICAN-COLLEGE OF CHEST PHYSICIANS SOCIETY OF CRITICAL CARE MEDICINE CONSENSUS CONFERENCE - DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ ;
ABRAMS, JH ;
BERNARD, GR ;
BIONDI, JW ;
CALVIN, JE ;
DEMLING, R ;
FAHEY, PJ ;
FISHER, CJ ;
FRANKLIN, C ;
GORELICK, KJ ;
KELLEY, MA ;
MAKI, DG ;
MARSHALL, JC ;
MERRILL, WW ;
PRIBBLE, JP ;
RACKOW, EC ;
RODELL, TC ;
SHEAGREN, JN ;
SILVER, M ;
SPRUNG, CL ;
STRAUBE, RC ;
TOBIN, MJ ;
TRENHOLME, GM ;
WAGNER, DP ;
WEBB, CD ;
WHERRY, JC ;
WIEDEMANN, HP ;
WORTEL, CH .
CRITICAL CARE MEDICINE, 1992, 20 (06) :864-874
[8]
BORDEN EC, 1994, J LAB CLIN MED, V123, P824
[9]
Polymorphisms IL10-819 and TLR-2 are potentially associated with sepsis in brazilian patients [J].
Carregaro, Fernanda ;
Carta, Adriana ;
Cordeiro, Jose Antonio ;
Lobo, Suzana M. ;
Tajara, Eloiza H. ;
Leopoldino, Andreia M. .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2010, 105 (05) :649-656
[10]
Interleukin-6 (-174C) polymorphism and the risk of sepsis in very low birth weight infants: meta-analysis [J].
Chauhan, M. ;
McGuire, W. .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2008, 93 (06) :1427-1429