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肿瘤坏死因子-α-308 G/A 多态性与鼻息肉的相关性。

Association of the tumor necrosis factor-alpha -308 G/A polymorphism with nasal polyposis.

机构信息

Otolaryngology Department, Elazig State Hospital, Elazig, Turkey.

出版信息

Eur Arch Otorhinolaryngol. 2010 Jun;267(6):903-8. doi: 10.1007/s00405-009-1167-5. Epub 2009 Dec 11.

DOI:10.1007/s00405-009-1167-5
PMID:20012441
Abstract

Nasal polyposis (NP) is a chronic inflammatory disease in which several molecular and cellular interactions play important roles. Tumor necrosis factor-alpha (TNF-alpha) is a major pro-inflammatory cytokine with a key role in immune inflammatory responses in NP. Altered levels of TNF-alpha, which may occur due to polymorphisms in the TNF-alpha promoter region, may also be associated with NP susceptibility. Given these facts, we investigated the possible association of the TNF-alpha -308 G/A single nucleotide polymorphism (SNP) with NP. In this study, 97 consecutive adult patients with NP and 95 age- and gender-matched controls were recruited. For identification of SNP, restriction fragment length polymorphism analysis after polymerase chain reaction was carried out. The NP group had a significantly higher rate of polymorphism compared to controls (p = 0.015). Logistic regression analysis revealed that the presence of the TNF-alpha -308 G/A SNP is an independent risk factor for NP development (OR, 3.68; CI, 1.27-10.7; p = 0.016). The presence of a mutation failed to influence disease severity on the basis of resistance to medical and/or surgical treatment. This study suggests a possible linkage of a SNP in the TNF-alpha promoter with NP. These results need to be confirmed with multicentre studies for more precise interpretation and corroborative studies for investigating the influence of polymorphism on transcriptional activity.

摘要

鼻息肉(NP)是一种慢性炎症性疾病,其中有几个分子和细胞相互作用起着重要作用。肿瘤坏死因子-α(TNF-α)是一种主要的促炎细胞因子,在 NP 的免疫炎症反应中起着关键作用。TNF-α水平的改变可能由于 TNF-α启动子区域的多态性而发生,也可能与 NP 易感性有关。鉴于这些事实,我们研究了 TNF-α-308 G/A 单核苷酸多态性(SNP)与 NP 之间的可能关联。在这项研究中,招募了 97 例连续的成年 NP 患者和 95 名年龄和性别匹配的对照者。为了鉴定 SNP,进行了聚合酶链反应后的限制性片段长度多态性分析。NP 组的多态性发生率明显高于对照组(p = 0.015)。逻辑回归分析显示,TNF-α-308 G/A SNP 的存在是 NP 发展的独立危险因素(OR,3.68;95%CI,1.27-10.7;p = 0.016)。突变的存在未能根据对药物和/或手术治疗的耐药性来影响疾病的严重程度。本研究提示 TNF-α 启动子中的 SNP 与 NP 之间可能存在联系。这些结果需要通过多中心研究进行更精确的解释和相关性研究来证实,以研究多态性对转录活性的影响。

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