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作 者:刘建平[1] 栗粟[1] 孙雅轩 LIU Jianping;LI Su;SUN Yaxuan(Department of Hepatological Surgery,Central Hospital of Panzhihua,Sichuan Province,Panzhihua 617067,China [)
机构地区:[1]四川省攀枝花市中心医院肝胆外科,四川攀枝花617067
出 处:《中国医药导报》2019年第1期68-73,共6页China Medical Herald
基 金:四川省科技厅科技支撑计划项目(2014SZ03614)
摘 要:目的统计分析白细胞介素-8(IL-8)基因启动子-251T>A多态性与急性胰腺炎(AP)发病风险的关系。方法对PubMed、Embase、Web of Science databases和万方数据库进行系统检索,检索IL-8启动子-251T>A多态性和急性胰腺炎发病风险相关的文献,文献查找日期为1990年1月~2015年12月。结果最终有7篇文献共计2282例病例纳入本研究。其中AP组病例1013例,对照组病例1269例。在纳入的总体中,IL-8启动子-251T>A多态性和AP发病风险相关(OR=1.56,95%CI:1.14~2.13,P=0.02);在显性模型中,A基因携带者会增加AP发病风险(OR=1.44,95%CI:1.21~1.73,P=0.01);在隐性模型中,纯合子AA基因型也会增加AP发病风险(OR=1.65, 95%CI:1.13~2.41,P=0.02)。亚组分析提示,IL-8启动子-251A多态性MAP隐性基因模型(OR=2.01,95%CI:1.25~3.24,P=0.025)和SAP所有基因模型(OR=1.80,95%CI:1.43~2.26,P=0.022;显性模型OR=2.17,95%CI:1.54~3.06,P=0.014;隐性模型OR=2.39,95%CI:1.49~3.81,P=0.005)会增加与AP发病风险。结论 IL-8基因启动子-251T>A多态性可能会增加AP的发病风险。但是考虑到本研究的局限性,需要有设计更完善、样本量更大的研究来证实该结论。Objective To investigate the relationship between the polymorphism of interleukin-8(IL-8)gene promoter-251T>A with the risk of acute pancreatitis(AP).Methods PubMed,Embase,Web of Science databases and WanFang were searched for studies on IL-8 promotor-251T>A polymorphism and AP risk from January 1990 to December 2015.Results Finally,seven studies involving 2282 cases,among all the cases,1013 in the AP group and 1269 in the control group.Among the population enrolled,IL-8 promoter-251T>A polymorphism was related to AP risk(OR=1.56,95%CI:1.41-2.13,P=0.02).In the dominant models,A carrier increased AP risk(OR=1.44,95%CI:1.21-1.73,P=0.01);in the recessive models,homozygote AA increased AP risk(OR=1.65,95%CI:1.13-2.41,P=0.02).Subgroup analysis indicated that the recessive gene model of MAP(OR=2.01,95%CI:1.25-3.24,P=0.025)and all SAP gene models(OR=1.80,95%CI:1.43-2.26,P=0.022),the dominant model(OR=2.17,95%CI:1.54-3.06,P=0.014)and the recessive model(OR=2.39,95%CI:1.49-3.81,P=0.005)of IL-8 promoter-251T>A polymorphism increased the risk of AP.Conclusion IL-8 promoter-251T>A is associated with increase of AP risk,but considering the limitations of this study,further research with better design and larger sample size is needed to confirm the conclusion.
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