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SOD2 基因 47C 等位基因(rs4880)的败血症患者中,脓毒性休克的频率更高。

Higher frequency of septic shock in septic patients with the 47C allele (rs4880) of the SOD2 gene.

机构信息

FABIO-PUCRS, Brazil.

出版信息

Gene. 2013 Mar 15;517(1):106-11. doi: 10.1016/j.gene.2012.10.078. Epub 2012 Nov 8.

Abstract

AIM

To analyze the effect of the two different versions of the manganese superoxide dismutase gene (SOD2) on sepsis. The SOD2 gene presents the 47C>T single nucleotide polymorphism (SNP; ID: rs4880) which produces MnSOD with different activities. The -9Val MnSOD (47T allele) is less efficient than the -9Ala version (47C allele). During sepsis there are abundance of ROS, high SOD2 expression and excess of H(2)O(2) synthesis. High concentrations of H(2)O(2) could affect the sepsis scenario and/or the sepsis outcome.

METHODS

We determined the 47C>T single nucleotide polymorphism (SNP) frequencies in 529 critically ill patients with or without sepsis, facing outcome. To collect information on population frequencies, we obtained a pilot 47C>T genotypic and allelic frequencies in a random group of 139 healthy subjects.

RESULTS

We compared the 47C allele carriers (47CC+47CT genotypes) with 47TT homozygotes and noticed a significant association between 47C allele carriers and septic shock in septic patients (P=0.025). With an adjusted binary multivariate logistic regression, incorporating 47C>T SNP and the main clinical predictors, we showed high SOFA scores [P<0.001, OR=9.107 (95% CI=5.319-15.592)] and 47C allele [P=0.011, OR=2.125 (95% CI=1.190-3.794)] were significantly associated with septic shock outcome. With this information we presented a hypothesis suggesting that this negative outcome from sepsis is possibly explained by effects on cellular stress caused by 47C allele.

CONCLUSION

In our population there was a significant higher frequency of septic shock in septic patients with the 47C allele of the SOD2 gene. This higher 47C allele frequency in septic patients with negative outcome could be explained by effects of higher activity MnSOD on cellular stress during the sepsis.

摘要

目的

分析两种不同版本的锰超氧化物歧化酶基因(SOD2)对脓毒症的影响。SOD2 基因存在 47C>T 单核苷酸多态性(SNP;ID:rs4880),导致 MnSOD 活性不同。-9Val MnSOD(47T 等位基因)的效率低于-9Ala 版本(47C 等位基因)。在脓毒症中,存在大量 ROS、SOD2 高表达和 H2O2 合成过量。高浓度的 H2O2 可能影响脓毒症的发生和/或结局。

方法

我们在 529 名危重病患者中确定了有无脓毒症和结局的情况下 47C>T 单核苷酸多态性(SNP)的频率。为了收集人群频率信息,我们在随机抽取的 139 名健康受试者中获得了 47C>T 基因型和等位基因频率的初步数据。

结果

我们比较了 47C 等位基因携带者(47CC+47CT 基因型)与 47TT 纯合子,发现脓毒症患者中 47C 等位基因携带者与感染性休克之间存在显著关联(P=0.025)。通过纳入 47C>T SNP 和主要临床预测因子的二元多变量逻辑回归,我们显示出较高的 SOFA 评分[P<0.001,OR=9.107(95%CI=5.319-15.592)]和 47C 等位基因[P=0.011,OR=2.125(95%CI=1.190-3.794)]与感染性休克结局显著相关。根据这些信息,我们提出了一个假设,即脓毒症中这种负面结局可能是由 47C 等位基因引起的细胞应激的影响所解释的。

结论

在我们的人群中,脓毒症患者中 SOD2 基因的 47C 等位基因的感染性休克发生率显著更高。脓毒症患者中具有负性结局的较高 47C 等位基因频率可能是由于较高活性 MnSOD 在脓毒症期间对细胞应激的影响所致。

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