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Association Between Single Nucleotide Polymorphisms of the Interleukin-4 Gene and Atopic Dermatitis Pubmed



Gharagozlou M1 ; Behniafard N1, 2 ; Amirzargar AA3 ; Hosseinverdi S2 ; Sotoudeh S1 ; Farhadi E4 ; Khaledi M5 ; Aryan Z2 ; Moghaddam ZG1 ; Mahmoudi M6 ; Aghamohammadi A1, 2 ; Rezaei N1, 2, 3, 7
Authors
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Authors Affiliations
  1. 1. Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Molecular Immunology Research Center, Department of Immunology-School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Hematology Department, School of Allied Medical Science, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. School of Nutrition and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Universal Scientific Education and Research Network (USERN), Teheran, Iran

Source: Acta Dermatovenerologica Croatica Published:2015


Abstract

Atopic dermatitis (AD) is an inflammatory skin disease in which both genetic and environmental factors seem to be involved. Several studies investigated the association of certain genetic factors with AD in different ethnic groups, but conflicting data were obtained. This study was performed to check the possible association between single nucleotide polymorphisms (SNPs) of interleukin 4 (IL-4) and the IL-4 receptor α chain (IL-4Rα) and AD in a group of Iranian patients. The allele and genotype frequencies of genes encoding for IL-4 and IL-4Rα were investigated in 89 patients with AD in comparison with 139 healthy controls, using methods based on polymerase chain reaction sequence-specific primers. The most frequent alleles of IL-4 in patients were T at -1098 (P<0.001, odds ratio (OR)=2.35), C at -590 (P<0.001, OR=4.84) and C at -33 (P=0.002, OR=2.08). The most frequent genotypes of IL-4 in patients were TT, CC, and CC at positions -1098 (P<0.001, OR=3.59), -590 (P<0.001, OR=31.25) and -33 (P<0.001, OR=3.46), respectively. We found a significant lower frequency of GT at -1098 GT, TC at -590, and TC at -33 in patients. There were no statistically significant differences in the frequency of alleles and genotypes of IL-4Rα gene at position +1902. A strong positive association was seen between TCC haplotype and AD (68% in patients vs. 23.4% in controls, P<0.001, OR=8.91). We detected a significantly lower frequency of TTC, GCC, and TTT haplotypes (P<0.001, OR=0.02, P<0.001, OR=0.40, P<0.001, OR=0.39, respectively) in patients compared to controls. A significant association between the polymorphisms of the IL-4 gene promoter at positions -1098, -590, and -33 and AD was detected in the Iranian population. © 2015, Croatian Dermatovenerological Society. All rights reserved.