Immune response and gene polymorphism profiles in Crohn's disease and ulcerative colitis

Inflamm Bowel Dis. 2009 Mar;15(3):353-8. doi: 10.1002/ibd.20757.

Abstract

Background: Polymorphisms in genes linked to the innate and adaptive immune response may be involved in inflammatory bowel disease pathogenesis. Our aim was to investigate associations among IL1B-511, IL1B-31, IL1RN, TNFA-307, TLR-2, TLR-4, IL2-330, NOD2 G908R, NOD2 L1007fsinsC polymorphisms and both Crohn's disease (CD) and ulcerative colitis (UC) in a Brazilian population.

Methods: We studied 43 patients with CD, 42 with UC, and 541 blood donors. Polymorphisms were evaluated by PCR, PCR-CTPP, or PCR-RFLP. Data were analyzed in multivariate models adjusting for confounding factors.

Results: IL1RN VNTR (P = 0.00, odds ratio [OR] = 2.43, 95% confidence interval [CI] = 1.50-3.90), as well as TNFA-307 polymorphic allele (P = 0.05, OR = 1.70, 95% CI = 1.00-2.94) were associated with UC. Both NOD2 mutations (G908R, P = 0.02, OR = 6.83, 95% CI = 1.62-25.45, and L1007fsinsC, P = 0.00, OR = 20.00, 95% CI = 3.21-124.69) were associated with CD.

Conclusions: Our analyses showed positive associations between proinflammatory polymorphisms at IL1RN and TNFA-307 loci and UC, as well as polymorphisms in the NOD2 gene and CD. These results highlight the importance of different genetic profiles associated with CD and UC.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Brazil / epidemiology
  • Colitis, Ulcerative / epidemiology
  • Colitis, Ulcerative / genetics
  • Colitis, Ulcerative / immunology*
  • Crohn Disease / epidemiology
  • Crohn Disease / genetics
  • Crohn Disease / immunology*
  • DNA / genetics*
  • Female
  • Follow-Up Studies
  • Genotype
  • Humans
  • Immunity, Cellular / immunology*
  • Interleukin 1 Receptor Antagonist Protein / genetics
  • Interleukin 1 Receptor Antagonist Protein / metabolism
  • Linkage Disequilibrium
  • Male
  • Nod2 Signaling Adaptor Protein / genetics*
  • Nod2 Signaling Adaptor Protein / metabolism
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Prevalence
  • Retrospective Studies

Substances

  • IL1RN protein, human
  • Interleukin 1 Receptor Antagonist Protein
  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein
  • DNA