Lack of association between intercellular adhesion molecule-1 gene polymorphisms and giant cell arteritis

J Rheumatol. 2001 Jul;28(7):1600-4.

Abstract

Objective: Studies have shown an association between HLA-DRB1*04 and giant cell arteritis (GCA). Intercellular adhesion molecule-1 (ICAM-1) gene polymorphisms were reported to contribute susceptibility to GCA in Italian patients where susceptibility to GCA is not associated with HLA-DRB1*04 alleles. ICAM-1 is also highly expressed within inflammatory infiltrates of the blood vessels of GCA patients. To investigate the clinical implications of ICAM-1 polymorphisms in GCA, we examined their potential association and influence in the development of visual ischemic complications in a series of patients with GCA from Northwest Spain where GCA susceptibility is associated with HLA-DRB1*04.

Methods: Fifty-eight biopsy proven GCA and 129 ethnically matched controls were studied. Patients and controls were genotyped for ICAM-1 polymorphism at codons 241 and 469 by PCR-RFLP.

Results: The distribution of the alleles and genotypes for each ICAM- polymorphism did not show significant differences between GCA patients and controls. Although visual manifestations were significantly more likely to occur in men than women (OR 5.2, p = 0.018), allele and genotype frequencies of ICAM-1 polymorphisms in patients with GCA were not associated with development of visual complications or anemia. Visual complications in GCA were primarily associated with carriage of an HLA-DRB1*04 allele. No evidence was found for interaction between HLA-DRB1*04 and ICAM-1 polymorphism.

Conclusion: ICAM-1 polymorphisms are not genetic risk factors for the susceptibility and severity of GCA in Northwest Spain.

MeSH terms

  • Aged
  • Anemia / genetics
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Giant Cell Arteritis / epidemiology
  • Giant Cell Arteritis / genetics*
  • HLA-DR Antigens / genetics
  • HLA-DRB1 Chains
  • Humans
  • Intercellular Adhesion Molecule-1 / genetics*
  • Ischemia / genetics
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Risk Factors
  • Vision Disorders / genetics

Substances

  • HLA-DR Antigens
  • HLA-DRB1 Chains
  • Intercellular Adhesion Molecule-1