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转化生长因子-β1 启动子变异 -509 c/t 与印度南部人群支气管哮喘的相关性。

Association of transforming growth factor-Beta 1 promoter variant -509 c/t with bronchial asthma in South Indian population.

机构信息

Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Hyderabad, 500016, India,

出版信息

Inflammation. 2015 Feb;38(1):409-14. doi: 10.1007/s10753-014-0045-5.

DOI:10.1007/s10753-014-0045-5
PMID:25359706
Abstract

Transforming growth factor-beta 1 (TGF-β1) is a multifunctional cytokine that plays a pivotal role in airway remodeling observed in the asthmatic airways. C to T base substitution at -509 promoter position in the TGF-β1 gene leads to its increased expression which contributes to airway remodeling in bronchial asthma. We sought to evaluate the association of TGF-β1 -509 C/T promoter variant with clinical asthma and varying degrees of disease severity. Three hundred and eighty-two clinically diagnosed asthma patients and 410 healthy controls were enrolled for the study. Patients were classified into severity classes according to the Global Initiative for Asthma (GINA) guidelines. TGF-β1 -509 C/T genotyping was carried out by amplification refractory mutation system polymerase chain reaction (ARMS-PCR) technique. In the present study, we found significantly higher frequency of TT genotype in asthma patients compared to controls (for TT vs. CC, p = 0.020). In addition, a significant difference was observed in the frequency of C and T allele in patients and controls (for T vs. C, p = 0.029). The heterozygous "CT" genotype was higher in moderate and severe asthmatics compared to mild subset of patients (for mild vs. moderate, p = 0.037). However, there was no significant distribution and association of variant allele with the severity subsets.

摘要

转化生长因子-β1(TGF-β1)是一种多功能细胞因子,在哮喘气道中观察到的气道重塑中发挥关键作用。TGF-β1 基因启动子位置-509 处的 C 到 T 碱基取代导致其表达增加,这有助于支气管哮喘的气道重塑。我们试图评估 TGF-β1-509C/T 启动子变异与临床哮喘和不同严重程度的相关性。招募了 382 名临床诊断为哮喘的患者和 410 名健康对照者进行研究。根据全球哮喘倡议(GINA)指南,将患者分为严重程度类别。采用扩增受阻突变系统聚合酶链反应(ARMS-PCR)技术对 TGF-β1-509C/T 基因分型进行了检测。在本研究中,我们发现哮喘患者 TT 基因型的频率明显高于对照组(TT 与 CC,p=0.020)。此外,患者和对照组中 C 和 T 等位基因的频率也存在显著差异(T 与 C,p=0.029)。与轻度哮喘患者相比,中度和重度哮喘患者的杂合“CT”基因型更高(轻度与中度,p=0.037)。然而,变异等位基因与严重程度亚组之间没有明显的分布和相关性。

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