Polymorphism of monocyte chemoattractant protein 1 in Crohn's disease

Int J Colorectal Dis. 2003 Sep;18(5):401-5. doi: 10.1007/s00384-003-0477-0. Epub 2003 Feb 1.

Abstract

Background and aims: The chemokine MCP-1 is thought to be important for the recruitment of mononuclear cells and the maintenance of inflammation in inflammatory bowel disease. We investigated whether MCP-1 protein expression is correlated with the degree of mucosal inflammation in patients with Crohn's disease. Furthermore, we studied whether a functional single nucleotide polymorphism (G or A) located in the distal regulatory region of the MCP-1 gene is associated with Crohn's disease and/or its phenotype.

Patients and methods: MCP-1 concentration in tissue homogenates was analyzed in mucosal biopsy specimens of 31 patients with Crohn's disease and 48 controls by enzyme-linked immunosorbent assay, and the correlation with an endoscopic macroscopic score was analyzed. In 179 patients with Crohn's disease and 189 controls MCP-1 genotyping was carried out by polymerase chain reaction restriction fragment length polymorphism technique. Subgroup phenotypic analysis was performed according to the Vienna classification.

Results: MCP-1 tissue concentrations were significantly associated with the macroscopic degree of inflammation. The gene frequency of the different MCP-1 alleles did not differ from healthy controls. However, the G/A and G/G genotype was significantly decreased in patients with a later onset of the disease and both genotypes presented also less frequently with a fistulizing disease behavior.

Conclusion: The degree of intestinal inflammation in Crohn's disease is associated with MCP-1 tissue levels. Furthermore there is evidence for an association of different disease behavior with different MCP-1 genotypes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Case-Control Studies
  • Chemokine CCL2 / genetics*
  • Chemokine CCL2 / metabolism
  • Colon / metabolism
  • Colon / pathology
  • Crohn Disease / genetics*
  • Crohn Disease / metabolism
  • Gene Frequency*
  • Genotype
  • Humans
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Phenotype*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Retrospective Studies

Substances

  • Chemokine CCL2