Title of article :
Association Study of TNF-α -308 G/A (rs1800629) and -863 C/A (rs1800630) Polymorphisms with Systemic Lupus Erythematosus in the Iranian Lor Population
Author/Authors :
Mashayekh ، Zeynab Department of Biology - Faculty of Science - Shahid Chamran University of Ahvaz , Rafieian ، Mahsa Department of Biology - Faculty of Science - Shahid Chamran University of Ahvaz , Kazeminezhad ، Reza Department of Biology - Faculty of Science - Shahid Chamran University of Ahvaz
From page :
1
To page :
6
Abstract :
Background:Systemic lupus erythematosus (SLE) is caused by a combination of environmental and genetic factors; studying the association between regulatory genes and this disease may determine the genetic causes of interfering with SLE. In different populations, studies have shown that the tumor necrosis factor α ( TNF-α) gene (as a candidate gene) can contribute to the formation and progression of lupus disease. Objectives: This study aimed to indicate the possible association between the increased rate of SLE hazard and 2 single-nucleotide polymorphisms (SNPs) of rs1800629 and rs1800630 genetic polymorphisms in the TNF-αpromoter gene in the Lor population. Methods: According to the American College of Rheumatology (ACR) criteria, 120 unrelated SLE patients and 120 healthy controls with no family or personal history of autoimmune diseases were selected. DNA was genotyped for the TNF-αpromoter (-308 G/A and -863 C/A) by the tetra-primer amplification-refractory mutation system (tetra-primer ARMS)–polymerase chain reaction (PCR) method. Results: The frequency difference between allele A (mutant allele) and allele C (normal allele) at position -863 of the TNF-αpromoter gene (odds ratio [OR] = 3.426; 95% CI, 1.985 - 5.914) was notably higher in SLE patients than in control subjects. Also, a significant relation was obtained among the rs1800830 AA genotype and increased risk of SLE (OR = 4.489; 95% CI, 2.464 - 8.177; P 0.0001). Our results for rs1800629 at position -308 were not remarkably different. Conclusions: We found a significant correlation between allelic and genotype frequencies between rs1800830 (-863 C/A) TNF-αSNP and SLE in our study. However, no significant correlation was observed between the rs1800629 (-308 G/A) TNF-αpromoter and the increase of SLE hazard in the Lor population. No remarkable association was obtained between TNF-αgene rs1800629 (-308 G/A) and rs1800630 (-863 C/A) SNPs and anti-double-stranded DNA (anti-dsDNA) or antinuclear antibody (ANA), which are some of the symptoms of SLE.
Keywords :
Systemic Lupus Erythematosus , Single , nucleotide Polymorphism , rs1800629 , rs1800630
Journal title :
Gene Cell Tissue
Journal title :
Gene Cell Tissue
Record number :
2739894
Link To Document :
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