AI Article Synopsis

  • This study explored how specific genetic variations (SNPs) in the TNF gene influence the risk of developing sepsis, using updated Sepsis-3 definitions.
  • It analyzed DNA from patients with infections and systemic inflammatory responses, comparing haplotypes and serum TNF-α levels.
  • The findings indicated that certain haplotypes associated with lower frequency alleles might reduce sepsis risk, but higher levels of TNF-α were found in patients with the more common haplotype who did develop sepsis.

Article 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.

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Source
http://dx.doi.org/10.1016/j.ijid.2017.12.008DOI Listing

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