Abstract
To investigate the possible role of the polymorphism located in the regulatory region of monocyte chemoattractant protein-1 (MCP-1) gene in the susceptibility to rheumatoid arthritis (RA), a total of 141 Spanish RA patients and 194 controls, previously typed for human leukocyte antigen DRB1* (HLA-DRB1*), were genotyped for -2518 (A/G) MCP-1 gene polymorphism using polymerase chain reaction–restriction fragment length polymorphism. No association between -2518 (A/G) MCP-1 polymorphism and susceptibility to RA was found. Nevertheless, when patients and controls were stratified according to their HLA shared epitope (SE) status, a significant increase in the frequency of genotype GG was found among SE negative (SE−) patients with respect to both SE positive (SE+) patients and SE− controls (16% versus 4% in SE+ patients, p Fisher = 0.04, odds ratio [OR] = 4.4, 95% confidence interval [95%CI] = 1.03–21.48; and 4% in SE− controls, p Fisher = 0.02, OR = 4.13, 95%CI = 1.10–15.72). In conclusion, MCP-1 polymorphism is slightly associated with the susceptibility to RA in patients lacking the HLA SE.
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