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白细胞介素-1家族细胞因子内的基因多态性影响脓毒症患者的预后

[Genomic polymorphism within interleukin-1 family cytokines influences the outcome of septic patients].

作者信息

Ma Penglin, Chen Dechang, Pan Jiaqi, Du Bin

机构信息

Department of Critical Care Medicine, Peking Union Medical College Hospital, Beijing 100730, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2002 Sep 25;82(18):1237-41.

Abstract

OBJECTIVE

To determine the allele frequencies and genotype distribution of interleukin (IL)-1 alpha, IL-1 beta and IL-1 receptor antagonist (IL-1ra) gene polymorphism in septic patients.

METHODS

A prospective, consecutive entry study was made among 60 patients with the diagnosis of sepsis who were admitted consecutively into the general intensive care unit (ICU), Peking Union Medical College Hospital between 1997 and 1999. APACHE II scoring and MODS scoring were made within 24 hours after admission. The genomic DNA of peripheral blood nucleated cells was extracted. The polymorphic regions within intron 6 of IL-1 alpha gene containing variable numbers of a tandem repeat (VNTR) of 46 bp, and intron 2 of IL-1ra gene containing VNTR of 86 bp were amplified by means of polymerase chain reaction (PCR). Alleles A1-4 and RN1-4 were identified according to the size of amplified DNA product. The region containing the AvaI polymorphic site at position -511 of IL-1 beta gene was amplified by PCR, and subsequently digested with AvaI restriction enzyme.

RESULTS

The frequencies of allele IL-1ra RN2 and genotype RN2/2 in the 60 septic patients were significantly higher than those in normal controls (0.34 vs 0.23, P < 0.01, and 0.12 vs 0.05, P < 0.05, respectively). The allele frequencies or genotype distribution of IL-1 alpha VNTR gene polymorphism and IL-1 beta AvaI polymorphism did not differ between the septic patients and normal controls. In addition, genotypes A2/2, B2/2 and RN2/2 were associated with a significantly higher mortality (80%, 81% and 71%, respectively) in septic patients. Patients with any 2 of the three alleles, i.e. A2, B2 and RN2, suffered from a much more severe sepsis (as measured by APACHE II and MODS scores) and higher mortality rate ( 55-65%), while septic patients with genotypes A1/1, B1/1 or RN1/1 showed a much lower mortality (0-13%).

CONCLUSION

Allele IL-1RN2 polymorphism, but not IL-1A or IL-1B gene polymorphism, is associated with susceptibility to sepsis. Alleles A2, B2 and RN2 might be important high-risk genetic markers for sepsis.

摘要

目的

确定脓毒症患者白细胞介素(IL)-1α、IL-1β和IL-1受体拮抗剂(IL-1ra)基因多态性的等位基因频率和基因型分布。

方法

对1997年至1999年期间连续入住北京协和医院综合重症监护病房(ICU)的60例脓毒症诊断患者进行前瞻性、连续入组研究。入院后24小时内进行急性生理与慢性健康状况评分系统(APACHE II)评分和多器官功能障碍综合征(MODS)评分。提取外周血有核细胞的基因组DNA。通过聚合酶链反应(PCR)扩增IL-1α基因第6内含子中含有46 bp串联重复序列(VNTR)可变数目的多态性区域,以及IL-1ra基因第2内含子中含有86 bp VNTR的区域。根据扩增DNA产物的大小鉴定等位基因A1-4和RN1-4。通过PCR扩增IL-1β基因-511位含AvaI多态性位点的区域,随后用AvaI限制酶消化。

结果

60例脓毒症患者中,等位基因IL-1ra RN2和基因型RN2/2的频率显著高于正常对照组(分别为0.34对0.23,P<0.01;0.12对0.05,P<0.05)。脓毒症患者与正常对照组之间,IL-1α VNTR基因多态性和IL-1β AvaI多态性的等位基因频率或基因型分布无差异。此外,基因型A2/2、B2/2和RN2/2的脓毒症患者死亡率显著更高(分别为80%、81%和71%)。具有三个等位基因(即A2、B2和RN2)中任意两个的患者脓毒症病情更严重(以APACHE II和MODS评分衡量),死亡率更高(55%-65%),而基因型为A1/1、B1/1或RN1/1的脓毒症患者死亡率则低得多(0%-13%)。

结论

与脓毒症易感性相关的是等位基因IL-1RN2多态性,而非IL-1A或IL-1B基因多态性。等位基因A2、B2和RN2可能是脓毒症重要的高危遗传标志物。

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