Clinical relevance of the TLR4 11367 polymorphism in patients with major trauma

Arch Surg. 2009 Dec;144(12):1144-8. doi: 10.1001/archsurg.2009.211.

Abstract

Objective: To investigate the clinical relevance of the TLR4 11367 polymorphism in patients with major trauma.

Design: Genetic functional and association study.

Setting: Daping Hospital and Chongqing Emergency Medical Center, Chongqing, China.

Patients: A total of 132 patients with major trauma were prospectively recruited.

Main outcome measures: The TLR4 11367 polymorphism was genotyped using single-tube, bidirectional, allele-specific amplification method. Whole peripheral blood samples obtained within 24 hours after admission were stimulated with lipopolysaccharide and then tested for production of tumor necrosis factor alpha and interleukin 6. Sepsis morbidity rate and multiple organ dysfunction scores were assessed.

Results: The 11367 polymorphism was shown to be strongly associated with less capacity of peripheral leukocytes to produce tumor necrosis factor alpha and interleukin 6 in response to ex vivo lipopolysaccharide stimulation in patients with trauma at admission. Results from association study indicated that patients with trauma who carry the 11367C allele were less likely to have sepsis and multiple organ dysfunction.

Conclusions: Combined with our previous in vitro functional study, the results suggest that the TLR4 11367 polymorphism might be a good predictor of who is more likely to develop complications such as sepsis or multiple organ dysfunction syndrome, depending on genotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Asian People / genetics
  • China
  • Cohort Studies
  • Female
  • Genotype
  • Humans
  • Injury Severity Score
  • Male
  • Middle Aged
  • Multiple Organ Failure / epidemiology
  • Multiple Organ Failure / genetics*
  • Polymorphism, Genetic / genetics*
  • Sepsis / epidemiology
  • Sepsis / genetics*
  • Toll-Like Receptor 4 / genetics*
  • Wounds and Injuries / complications*
  • Wounds and Injuries / genetics*
  • Young Adult

Substances

  • TLR4 protein, human
  • Toll-Like Receptor 4