INTERLEUKIN-4 (IL-4) AND INTERLEUKIN-4 RECEPTOR ALPHA CHAIN (IL-4Rα) GENE POLYMORPHISMS IN EGYPTIAN RHEUMATIC ARTHRITIS PATIENTS | ||||
Biochemistry Letters | ||||
Article 1, Volume 7, Issue 1, 2011, Page 1-21 PDF (2.55 MB) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/blj.2010.64239 | ||||
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Authors | ||||
Faten Z. Mohamed1; Yousri M. Mussien2; Eman F. Basiony3 | ||||
1Biochemistry Division, Dept. of Chemistry, Faculty of Science, Zagazig University | ||||
2Faculty of Medicine, Zagazig University, Egypt | ||||
3Faculty of Medicine, Zagazig University, Egypt. | ||||
Abstract | ||||
Rheumatoid arthritis (RA) is considered a Th1-driven disease. Interleukin 4 (IL-4) binds to its receptor, promoting Th2 differentiation and limiting Th1 responses, but its role in the pathogenesis of RA is conflicting. Objective: to evaluate the occurrence of variants of interleukin-4 (IL-4) and Interleukin-4 Receptor Alpha chain (IL-4 RA) gene in patients with rheumatoid arthritis and their possible contribution to disease severity. Methods: We analyzed 2 polymorphisms of the IL4 gene and 2 polymorphisms of IL-4 RA in patients with RA and in a control population, as well as measuring serum RF as a disease severity parameter. Results: The IL-4 –590 TT genotype (P<0.001) and The IL4 –590T allele (OR 2.84, 95% CI 1.0-8.77, p=0.03) were significantly more frequent in patients with RA than in controls, this is similar for IL-4 VNTR RP1⁄RP1 genotype (P<0.001) and IL-4 RP1 allele (OR 2.91 CI 0.92-10.23, P=0.04). Higher frequency of IL-4 RA I50V genotypes (P= 0.02) in RA patients compared with controls were also found. Nevertheless, the more severe form of RA is observed in patients carrying the IL-4 -590 T allele as compared with homozygous patients. The IL-4RA Q576 allele and IL-4RA V50 allele were significantly associated with the sever form of RA. Conclusion: The IL-4 -590 C/T, IL-4 VNTR in intron-3 and IL-4Rα I50V polymorphism were associated with RA susceptibility in Egyptian population. IL-4Rα I50V and IL-4Rα Q576R polymorphisms may be may be a genetic risk factor for RA severity. | ||||
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