Suppr超能文献

没有证据表明谷胱甘肽 S-转移酶多态性与慢性鼻-鼻窦炎相关。

No evidence for a correlation of glutathione S-tranferase polymorphisms and chronic rhinosinusitis.

机构信息

Department of Otolaryngology, Head and Neck Surgery, University Medical Center of the Johannes Gutenberg University Mainz, Germany.

出版信息

Rhinology. 2011 Jun;49(2):180-4. doi: 10.4193/Rhino10.064.

Abstract

OBJECTIVE

Cellular detoxification mechanisms are mandatory for cellular protection against oxidative stress and reactive oxygen species. One major group of antioxidative active enzymes involved in cellular detoxification are the Glutathione S-Transferases (GST). Multiple subtypes like GSTM1, GSTP1, and GSTT1 and variants of them are known, arising from allelic variations of the GST loci. Moreover, functional variants occur in high percentages and have been associated with diseases like bronchial asthma and bronchial hyperresponsiveness. The interplay of oxidative stress, detoxifying genes like GSTs and the genesis of respiratory tract illness is under contradictory debate. In this study, we analysed the potential association of GST-polymorphisms and chronic rhinosinusitis (CRS).

METHODS

In total 170 nasal tissue samples, 49 tissue samples from patients with CRS without nasal polyps, 69 tissue samples from CRS with nasal polyps and 52 healthy tissue controls of the inferior turbinate were analysed for their individual GST-status. Genotypes for GSTM1 (null versus present), GSTT1 (null versus present), and GSTP1 (Ile105Val) were determined by Polymerase Chain Reaction. The respective genotypes were correlated to the incidence of CRS with and without nasal polyps in aspirin-tolerant and intolerant patients and to the individual health status concerning asthma and allergies.

RESULTS

No correlation between any GST-polymorphism and CRS with and without nasal polyps or allergies or asthma or aspirin-intolerance was observed.

CONCLUSION

Our results do not suggest that there is a relevant genetic predisposition considering the individual GST-status for the susceptibility of nasal respiratory epithelia leading to CRS.

摘要

目的

细胞解毒机制对于细胞抵御氧化应激和活性氧至关重要。参与细胞解毒的主要抗氧化酶之一是谷胱甘肽 S-转移酶 (GST)。有多种亚型,如 GSTM1、GSTP1 和 GSTT1 及其等位基因变异体,这些都是 GST 基因座的等位基因变异产生的。此外,功能变体的出现频率很高,并与支气管哮喘和支气管高反应性等疾病有关。氧化应激、解毒基因(如 GST)和呼吸道疾病发生之间的相互作用存在争议。在这项研究中,我们分析了 GST 多态性与慢性鼻-鼻窦炎 (CRS) 的潜在关联。

方法

总共分析了 170 个鼻组织样本,其中 49 个来自无鼻息肉的 CRS 患者,69 个来自有鼻息肉的 CRS 患者,52 个来自下鼻甲健康对照组的组织样本,以分析其个体 GST 状态。通过聚合酶链反应 (PCR) 确定 GSTM1(缺失型与存在型)、GSTT1(缺失型与存在型)和 GSTP1(Ile105Val)的基因型。将各自的基因型与阿司匹林耐受和不耐受患者中有无鼻息肉的 CRS 发生率以及与哮喘和过敏有关的个体健康状况相关联。

结果

未观察到任何 GST 多态性与有无鼻息肉的 CRS、过敏或哮喘或阿司匹林不耐受之间存在相关性。

结论

我们的结果表明,考虑到 GST 个体状态对导致 CRS 的鼻呼吸道上皮的易感性,没有与 GST 多态性相关的遗传易感性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验