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IL-10 polymorphism is associated with increased incidence of severe sepsis

机译:IL-10多态性与严重败血症的发生率增加相关

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摘要

Objective To investigate whether three biallelic polymorphisms at positions -592, -819 and -1082 in the promoter region of the IL-10 gene are associated with increased incidence of severe sepsis. Methods The IL-10 -592, -819 and -1082 polymorphisms were typed using polymerase chain reaction followed by digestion with the restriction enzymes Rsa I, Mae III and Mnl I, respectively. Results Patients with severe sepsis were more likely to have IL-10 -1082 allele 1, compared with controls (P<0. 05). Genotype distribution of the IL-10 -1082 polymorphism significantly differed between patients and controls (P<0. 05). However, the allele frequencies and genotype distribution of the IL-10 -1082 polymorphism did not differ between surviving and dead patients (P>0. 05). No significant differences in the genotype distribution and allele frequencies of the IL-10 -592 and IL-10 -819 polymorphisms were observed between patients with severe sepsis and heathy controls, nor between surviving and dead patients (P> 0. 05). Conclusions The polymorphism at position -1082 in the promoter region of the IL-10 gene may be associated with susceptibility to severe sepsis. In constrast, the other two highly linked IL-10 polymorphisms are not associated with incidence or the outcome of severe sepsis.
机译:目的探讨IL-10基因启动子区域-592,-819和-1082位的三个双等位基因多态性是否与严重败血症的发生率增加相关。方法采用聚合酶链式反应,分别用限制性内切酶Rsa I,Mae III和Mnl I消化,确定IL-10 -592,-819和-1082多态性。结果败血症严重的患者与对照组相比,更有可能患有IL-10 -1082等位基因1(P <0。05)。 IL-10 -1082多态性的基因型分布在患者和对照组之间有显着差异(P <0。05)。然而,存活和死亡患者之间IL-10 -1082多态性的等位基因频率和基因型分布没有差异(P> 0。05)。在患有严重脓毒症和健康对照的患者之间以及存活和死亡患者之间,IL-10 -592和IL-10 -819多态性的基因型分布和等位基因频率均未观察到显着差异(P> 0. 05)。结论IL-10基因启动子区-1082位点的多态性可能与严重脓毒症的易感性有关。相反,其他两个高度相关的IL-10多态性与严重败血症的发生率或结果无关。

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