The -A2518G polymorphism in the MCP-1 gene and inflammatory bowel disease risk: A meta-analysis

J Dig Dis. 2015 Apr;16(4):177-85. doi: 10.1111/1751-2980.12232.

Abstract

Objective: The monocyte chemoattractant protein-1 (MCP-1) -A2518G gene polymorphism has been found to be involved in the susceptibility to inflammatory bowel disease (IBD); however, the results of existing studies are controversial. The aim of this meta-analysis was to assess the relationship between the MCP-1 -A2518G polymorphism and the risk of IBD.

Methods: PubMed, EMBASE and MEDLINE were searched for studies assessing the relationship between the -A2518G polymorphism in MCP-1 gene and the risk of IBD. Available data were extracted and statistically analyzed using STATA 12.0.

Results: A total of five publications involving 3137 individuals (1818 IBD cases and 1319 controls) were included in the meta-analysis. A combined analysis revealed that the MCP-1 -A2518G polymorphism in was a protective factor for GG + AG vs AA (OR 0.76, 95% CI 0.67-0.87, P = 0.000). Subgroup analysis by ethnicity showed that among European patients the AG + GG homozygote, unlike the AA homozygote, had a protective effect against IBD (OR 0.73, 95% CI 0.63-0.84, P = 0.000), but did not do so among Asian and African patients. Subgroup analysis by disease subtype suggested the -A2518G polymorphism in MCP-1 had a protective effect against Crohn's disease (OR 0.69, 95% CI 0.58-0.81, P = 0.000), but not against ulcerative colitis.

Conclusions: Our meta-analysis suggested that the -A2518G polymorphism in MCP-1 may be a protective factor for IBD in European populations. Further studies are required to confirm these findings.

Keywords: inflammatory bowel disease; meta-analysis; monocyte chemoattractant protein-1; polymorphism; susceptibility.

Publication types

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

MeSH terms

  • Asian People / genetics
  • Black People / genetics
  • Chemokine CCL2 / genetics*
  • Genetic Predisposition to Disease
  • Humans
  • Inflammatory Bowel Diseases / genetics*
  • Polymorphism, Genetic / genetics*
  • White People / genetics

Substances

  • CCL2 protein, human
  • Chemokine CCL2