TNF-Alpha Gene Polymorphisms in Iranian Azari Turkish Patients with Inflammatory Bowel Diseases

被引:12
|
作者
Bonyadi, Mortaza [1 ]
Abdolmohammadi, Reza [1 ]
Jahanafrooz, Zohreh [2 ]
Somy, Mohammad-Hosein [1 ]
Khoshbaten, Manoochehr [1 ]
机构
[1] Tabriz Univ Med Sci, Liver & Gastrointestinal Dis Res Ctr, Tabriz, Iran
[2] Univ Tabriz, Fac Nat Sci, Ctr Excellence Biodivers, Dept Genet, Tabriz, Iran
来源
SAUDI JOURNAL OF GASTROENTEROLOGY | 2014年 / 20卷 / 02期
关键词
Genetics; inflammatory bowel disease; single nucleotide polymorphisms; tumor necrosis factor alfa; CROHNS-DISEASE; ULCERATIVE-COLITIS; PROMOTER; SUSCEPTIBILITY; METAANALYSIS; ASSOCIATION; IL-10;
D O I
10.4103/1319-3767.129475
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Context: Crohn's disease (CD) and ulcerative colitis (UC) are chronic inflammatory diseases of the bowel (IBD) whose causes are not fully known. Emerging data indicate that alterations in cytokine synthesis may play a role in IBD pathogenesis. Aims: We aimed to determine the association between tumor necrosis factor-alfa (TNF alpha) promoter polymorphisms (at positions -308 and -1031) and susceptibility to IBD among Iranian Azari Turkish patients. Settings and Design: One hundred and one patients with IBD and 100 healthy subjects were analyzed. Materials and Methods: Both polymorphisms in the promoter region of the TNF alpha gene at positions -1031T/C and -308G/A were detected by polymerase chain reaction-restriction fragment length polymorphism assay. All statistical analyses were calculated with SPSS for Windows 16.0. The Fisher's exact test was used to test for departure from Hardy-Weinberg equilibrium of the genotype frequencies (P > 0.05). Results: The allele frequency of the TNF alpha-308G and -1031T were higher in IBD patients but did not reach statistical significance. However, the homozygous TT genotype for the SNP-1031 T > C was significantly higher in UC patients than in healthy controls (P = 0.01) and the heterozygous CT genotype for the SNP -1031 T > C was significantly lower in UC patients than in healthy controls (P = 0.03). Conclusions: The TNF alpha-1031 T allele confers a significant risk for developing UC in Iranian Azeri Turkish patients. Also the frequency of TNF alpha-1031 C allele was considerably low among patients with UC and it may have protective role among them (OR = 0.43; P = 0.01).
引用
收藏
页码:108 / 112
页数:5
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