Intercellular adhesion molecule-1 gene polymorphisms in isolated polymyalgia rheumatica
Amoli MM, ShelleyE, MatteyD.L, Garcia-PorruaC, Thomson W, HajeerA.H, Ollier WER, Gonzalez-GayM.A
Journal of Rheumatology. 2002;29, 3:502-504.
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OBJECTIVE: In untreated polymyalgia rheumatica (PMR), high levels of circulating soluble intercellular adhesion molecule-1 (ICAM-1) have been observed. To investigate the clinical implication of ICAM-1 polymorphisms in isolated PMR, we examined their potential influence in an unselected series of patients. METHODS: We studied 72 patients with isolated PMR and 129 ethnically matched controls from Lugo, Spain. Patients and controls were genotyped for HLA-DRB1 and ICAM-1 polymorphism at codons 241 and 469 by molecular methods. RESULTS: The distribution of alleles and genotypes for each ICAM-1 polymorphism did not show significant differences between patients with isolated PMR and controls. There were also no associations between ICAM-1 polymorphisms and relapses of the disease. The latter was primarily associated with carriage of an HLA-DRB1*0401 allele (OR 7.2, p = 0.01), although all relapsed patients with HLA-DRB1*0401 also carried the GG genotype of the ICAM-1 polymorphism at codon 241. The presence of both HLA-DRB1*0401 and the GG241 ICAM-1 genotype gave an OR of 15.2 (p = 0.005) after correction for age and sex. CONCLUSION: Although ICAM-1 polymorphisms alone do not appear to be associated with disease severity in isolated PMR, the presence of both HLA-DRB1*0401 and the ICAM-1 codon 241 GG homozygosity was significantly associated with increased risk of relapses in these patients
Alleles; Codon; Disease; Gene Frequency; Genotype; HLA-DR Antigens; Human; Intercellular Adhesion Molecule-1; Polymorphism (Genetics); Polymyalgia Rheumatica; Recurrence; Risk; Spain; Vasculitis; epidemiology; genetics; methods
- UI - 21905231DA - 20020322IS - 0315-162XLA - engPT - Journal ArticleRN - 0 (HLA-DR Antigens)RN - 126547-89-5 (Intercellular Adhesion Molecule-1)RN - 128338-86-3 (HLA-DRB1)SB - IM