Gene polymorphisms in the interleukins gene and the risk of acute pancreatitis: A meta-analysis

被引:5
|
作者
Zhu, Xiaole [1 ,2 ]
Hou, Chaoqun [1 ,2 ]
Tu, Min [1 ,2 ]
Shi, Chenyuan [1 ,2 ]
Yin, Lingdi [1 ,2 ]
Peng, Yunpeng [1 ,2 ]
Li, Qiang [1 ,2 ]
Miao, Yi [1 ,2 ]
机构
[1] Nanjing Med Univ, Pancreas Ctr, Affiliated Hosp 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Pancreas Inst, Nanjing 210029, Jiangsu, Peoples R China
关键词
Interleukin; Polymorphism; Acute pancreatitis; Meta-analysis; ASSOCIATION; SUSCEPTIBILITY; IL-8; CYTOKINE;
D O I
10.1016/j.cyto.2018.12.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Single nucleotide polymorphisms (SNPs) within the interleukins (IL) gene may affect the risk of acute pancreatitis. Many epidemiological studies have reported an association between the IL gene and acute pancreatitis risk, but the results remain inconsistent. Given the controversial available data, we carried out a meta-analysis to systematically evaluate and clarify the association between IL gene polymorphisms and AP. A systematic search of studies for this association was obtained from the PubMed, EMBASE, Web of Science and Chinese National Knowledge Infrastructure (CNKI) databases until June 1, 2017. We also searched the references of the included studies to identify additional studies. Odds ratios (ORs) with 95% confidence intervals (95% CIs) were used to pool the effect size. Stata12.0 was used for whole statistical analysis. Fifteen studies that contained 3371 AP cases and 3506 controls were included in final combination. Overall, a significant association was found between the IL-8-251 T/A (rs4073) polymorphism, the IL-10-1082 A/G (rs1800896) polymorphism and the AP risk in four genetic models (homozygote model, recessive model, dominant model, allele model). Meanwhile, individuals with IL-1 beta+3954 C/T (rs1143634, (homozygote model, recessive model)), IL-1 beta-511 C/T (rs16944, (dominant model)) and IL-6-634C/G (rs1800796, (allele model)) polymorphism were associated with an increased risk of AP. No evidence of an association was found between IL and 10-592 C/A (rs1800872) and IL-10-819 C/T (rs1800871) polymorphism and AP risk.
引用
收藏
页码:50 / 59
页数:10
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