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由 TNF 基因中较小频率单核苷酸多态性组成的单体型可预防向脓毒症进展:使用新的脓毒症分类的研究。

Haplotypes composed of minor frequency single nucleotide polymorphisms of the TNF gene protect from progression into sepsis: A study using the new sepsis classification.

机构信息

Department of Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.

Genome Analysis, Leibniz Institute on Aging - Fritz Lipmann Institute, Jena, Germany.

出版信息

Int J Infect Dis. 2018 Feb;67:102-106. doi: 10.1016/j.ijid.2017.12.008. Epub 2017 Dec 21.

DOI:10.1016/j.ijid.2017.12.008
PMID:29274398
Abstract

OBJECTIVES

Several articles have provided conflicting results regarding the role of single nucleotide polymorphisms (SNPs) in the promoter region of the TNF gene in susceptibility to sepsis. Former articles have been based on previous definitions of sepsis. This study investigated the influence of TNF haplotypes on the development of sepsis using the new Sepsis-3 definitions.

METHODS

DNA was isolated from patients suffering from infection and systemic inflammatory response syndrome. Haplotyping was performed for six SNPs of TNF. The serum levels of tumour necrosis factor alpha (TNF-α) of these patients were measured using an enzyme immunosorbent assay. Patients were classified into infection and sepsis categories using the Sepsis-3 definitions. Associations between the TNF haplotypes and the clinical characteristics and serum TNF-α levels of the patients were examined.

RESULTS

The most common TNF haplotype h1 was composed of major alleles of the studied SNPs. Carriage of haplotypes composed of minor frequency alleles was associated with a lower risk of developing sepsis (odds ratio 0.41, 95% confidence interval 0.19-0.88, p=0.022), but this did not affect the 28-day outcome. Serum TNF-α levels were significantly higher among patients homozygous for h1 haplotypes who developed sepsis compared to infection (p=0.032); a similar result was not observed for patients carrying other haplotypes.

CONCLUSIONS

Haplotypes containing minor frequency SNP alleles of TNF protect against the development of sepsis without affecting the outcome.

摘要

目的

有几篇文章对于肿瘤坏死因子(TNF)基因启动子区域单核苷酸多态性(SNPs)在脓毒症易感性中的作用提供了相互矛盾的结果。以前的文章基于以前的脓毒症定义。本研究使用新的 Sepsis-3 定义,调查了 TNF 单倍型对脓毒症发展的影响。

方法

从患有感染和全身炎症反应综合征的患者中提取 DNA。对 TNF 的六个 SNPs 进行单倍型分析。使用酶联免疫吸附试验测量这些患者的肿瘤坏死因子-α(TNF-α)血清水平。使用 Sepsis-3 定义将患者分为感染和脓毒症组。检查 TNF 单倍型与患者的临床特征和血清 TNF-α水平之间的关联。

结果

最常见的 TNF 单倍型 h1 由研究 SNP 的主要等位基因组成。携带由较小频率等位基因组成的单倍型与发生脓毒症的风险较低相关(优势比 0.41,95%置信区间 0.19-0.88,p=0.022),但这并不影响 28 天的结果。与携带其他单倍型的患者相比,发生脓毒症的 h1 单倍型纯合子患者的血清 TNF-α水平明显更高(p=0.032);对于携带其他单倍型的患者,未观察到类似的结果。

结论

含有 TNF 较小频率 SNP 等位基因的单倍型可预防脓毒症的发生,而不影响结局。

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