A novel 5'-flanking region polymorphism of macrophage migration inhibitory factor is associated with systemic-onset juvenile idiopathic arthritis

Arthritis Rheum. 2001 Aug;44(8):1782-5. doi: 10.1002/1529-0131(200108)44:8<1782::AID-ART314>3.0.CO;2-#.

Abstract

Objective: To determine if polymorphisms of the macrophage migration inhibitory factor (MIF) gene are associated with systemic-onset juvenile idiopathic arthritis (JIA).

Methods: Denaturing high-performance liquid chromatography was used to screen for the MIF gene in 32 healthy Caucasian subjects. One hundred seventeen UK Caucasian patients with systemic-onset JIA and 172 unrelated healthy UK Caucasian controls were genotyped for a single-nucleotide polymorphism (SNP) identified in the 5'-flanking region of the gene, using polymerase chain reaction-restriction fragment length analysis.

Results: A G-to-C transition was identified at position -173 of the MIF gene. The presence of a C at -173 creates an activator protein 4 transcription factor binding site. Allele and genotype frequencies differed significantly between the patients and controls for the MIF-173 polymorphism. Individuals possessing a MIF-173*C allele have an increased risk of systemic-onset JIA (36.8% versus 20.3%) (odds ratio 2.3, 95% confidence interval 1.34-3.86; P = 0.0005).

Conclusion: This is the first report of a SNP in the MIF gene. This polymorphism is associated with systemic-onset JIA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Untranslated Regions
  • Arthritis, Juvenile / genetics*
  • Child
  • Child, Preschool
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Humans
  • Infant
  • Macrophage Migration-Inhibitory Factors / genetics*
  • Polymorphism, Restriction Fragment Length
  • Polymorphism, Single Nucleotide*

Substances

  • 5' Untranslated Regions
  • Macrophage Migration-Inhibitory Factors