The fibrinogen -148 C/T polymorphism influences inflammatory response in experimental endotoxemia in vivo

Thromb Res. 2007;120(5):727-31. doi: 10.1016/j.thromres.2006.12.007. Epub 2007 Feb 15.

Abstract

Introduction: The acute phase reactant fibrinogen plays a critical role in the coagulation system and inflammation. Recently several polymorphisms have been described regulating basal and peak fibrinogen expression. We evaluated the role of a frequent promoter polymorphism in the beta chain of the fibrinogen gene (-148 C/T) in a human in vivo model of experimental endotoxemia.

Material and methods: Healthy volunteers received 2 ng/kg endotoxin (LPS, n=73) as a bolus infusion over 2 min. Blood samples were collected by venipunctures into EDTA anticoagulated vacutainer tubes before LPS infusion. For determination of the fibrinogen promoter polymorphism, we developed a new mutagenic separated polymerase chain reaction assay.

Results: Carriers of the -148 T allele had significantly lower TNFalpha expression throughout the whole time course of LPS stimulation and Interleukin-6 levels were trendwise lower, however only basal levels reached statistical significance. No effects were observed on markers of coagulation activation (D-Dimer, Prothrombin F(1+2)).

Conclusion: Our findings indicate, that the common -148 C/T polymorphism is associated with differences in the TNFalpha release in response to systemic LPS infusion in humans, and add to current evidence that gene-sequence changes in beta-fibrinogen locus can alter the ability of the host to respond to endotoxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Edetic Acid / chemistry
  • Endotoxemia / genetics*
  • Fibrinogen / genetics*
  • Fibrinogen / physiology*
  • Humans
  • Inflammation
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / metabolism
  • Male
  • Models, Biological
  • Mutagenesis
  • Polymerase Chain Reaction / methods*
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-6
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha
  • Fibrinogen
  • Edetic Acid