Association between interleukin 1 receptor antagonist gene 86-bp VNTR polymorphism and sepsis: A meta-analysis

被引:8
作者
Fang, Fang [1 ]
Pan, Jian [1 ]
Li, Yiping [1 ]
Xu, Lixiao [1 ]
Su, Guanghao [1 ]
Li, Gang [1 ]
Wang, Jian [1 ]
机构
[1] Soochow Univ, Childrens Hosp, Pediat Res Inst, Suzhou 215003, Jiangsu, Peoples R China
关键词
Interleukin 1 receptor antagonist; Polymorphism; Sepsis; Mortality; Meta-analysis; DISEASE; SEVERITY; MORTALITY; ALLELE; FAMILY;
D O I
10.1016/j.humimm.2014.12.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Objective: Many studies have focused on the relationship between interleukin 1 receptor antagonist (IL1RN) gene 86-bp VNTR polymorphism and sepsis, but the results remain inconsistent. Thus, a meta-analysis was carried out to derive a more precise estimation of the association between RJRN 86-bp VNTR polymorphism and risk of sepsis and sepsis-related mortality. Methods: Relevant publications were searched in several widely used databases and six eligible studies were included in the meta-analysis. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the strength of the association between IL1RN 86-bp VNTR polymorphism and risk of sepsis and sepsis-related mortality. Results: Significant associations between IL1RN 86-bp VNTR polymorphism and sepsis risk were observed in both overall meta-analysis for L2 versus 22 (OR = 0.75, 95% CI = 0.59-0.94) and severe sepsis subgroup for LL + L2 versus 22 (OR = 0.67, 95% CI = 0.47-0.93). L stands for long alleles containing three to six repeats; 2 stands for short allele containing two repeats. However, no significant sepsis mortality variation was detected for all genetic models. Conclusions: According to the results of our meta-analysis, the IL1RN 86-bp VNTR polymorphism probably associates with sepsis risk but not with sepsis-related mortality. (C) 2014 Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics.
引用
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页码:1 / 5
页数:5
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