TNFα-308 G/A 和 IFN-γ+874A/T 多态性与口腔扁平苔藓的关系

Q4 Medicine
Malihe Saleh Gohari, Molook Torabi, Reihaneh Saleh Gohari, Elham Abbaszadeh, N. Saleh-Gohari
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引用次数: 0

摘要

背景:口腔扁平苔藓(OLP)是一种表现为炎症的慢性疾病,全球发病率为 0.1-4%。该病的病变发生在口腔粘膜、牙龈,很少发生在腭部。本研究旨在探讨这种疾病与 TNFα-308G/A 和 IFN-γ+874A/T 多态性之间的关系。研究方法在这项病例对照研究中,我们收集了 50 名健康受试者的口腔黏膜样本,并采用简单抽样方法招募了 50 名到克尔曼牙科学院就诊的 OLP 患者。随后,我们使用扩增难治性突变系统聚合酶链式反应(ARMS-PCR)技术,通过测序确定病例和对照组中是否存在 TNFα-308G/A 和 IFN-γ+874A/T 多态性。结果显示与对照组相比,OLP患者TNF基因A和GA等位基因的发生率高于G和GG等位基因的发生率,而在OLP患者中未发现该基因的AA基因型。在 IFN 基因多态性方面,发现 T 等位基因与患病风险之间存在关系,但无统计学意义(P 值:0.068)。结论虽然TNF-α(-308G/A)多态性的A等位基因与OLP的发病风险有密切关系,但IFN-γ+874A/T基因型与疾病之间的关系不足以预测患OLP的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between TNFα-308 G/A and IFN-γ+874A/T Polymorphisms with Oral Lichen Planus
Background: Oral lichen planus (OLP) is a chronic disease that presents with inflammation and has a global prevalence of 0.1-4%. Lesions of the disease occur in the oral mucosa, gums, and rarely in the palate. This study aimed to investigate the relationship between this disease and TNFα-308G/A and IFN-γ+874A/T polymorphisms. Methods: In this case-control study, oral mucosal samples were collected from 50 healthy subjects, and 50 OLP patients presented to the Kerman Faculty of Dentistry were enrolled using a simple sampling method. Subsequently, we used the amplification refractory mutation system polymerase chain reaction (ARMS-PCR) technique followed by sequencing to determine the presence of TNFα-308G/A and IFN-γ+874A/T polymorphisms in cases and controls. Results: Compared to the control group, the prevalence of A and GA alleles of the TNF gene was higher than the prevalence of G and GG alleles in OLP patients, while the AA genotype of the gene was not found in OLP patients. Regarding IFN gene polymorphism, the relationship between the T allele and the risk of disease was discovered, but it was not statistically significant (P value: 0.068). Conclusion: Although there is a strong relation between the A allele of TNF-α (-308G/A) polymorphism and the risk of OLP, this association between IFN-γ+874A/T genotype and the disease was not strong enough to predict the possibility of developing OLP.
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