Association between lymphotoxin-α intron +252 polymorphism and sepsis: a meta-analysis

Scand J Infect Dis. 2011 Jul;43(6-7):436-47. doi: 10.3109/00365548.2011.562528. Epub 2011 Mar 2.

Abstract

Background: We evaluated the association of lymphotoxin-α (LTA, also known as tumour necrosis factor-β) promoter +252 A/G polymorphism with sepsis.

Methods: A systematic search was performed in MEDLINE, EMBASE, and Web of Science (for the period January 1966 to June 2010). Two reviewers independently selected studies on the genetic association of LTA +252 A/G polymorphism with sepsis and independently extracted data onto standardized forms.

Results: Twenty-seven studies with 4399 septic patients were included based on predefined inclusion criteria. As compared to AG + GG, the LTA AA genotype was significantly associated with an increased development of sepsis in the overall population (odds ratio (OR) 1.33, 95% confidence interval (CI) 1.09-1.62; p = 0.006). An association between mortality from sepsis and AA genotype was also found in the overall population (OR 1.89, 95% CI 1.27-2.80; p = 0.002). Stratification by ethnicity indicated that the contribution to both sepsis susceptibility and mortality may be stronger in Caucasians (OR 1.44, 95% CI 1.08-1.91 and OR 2.47, 95% CI 1.52-4.00, respectively) than in other ethnicities.

Conclusions: The LTA +252 A/G polymorphism is associated with both susceptibility to and mortality from sepsis.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Child
  • Child, Preschool
  • Ethnicity
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Infant
  • Infant, Newborn
  • Introns*
  • Lymphotoxin-alpha / genetics*
  • Lymphotoxin-alpha / immunology*
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Sepsis / genetics*
  • Sepsis / immunology*
  • Sepsis / mortality
  • Young Adult

Substances

  • Lymphotoxin-alpha