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首页> 外文期刊>Journal of occupational health >Lack of association between cytokine gene polymorphisms and silicosis and pulmonary tuberculosis in Chinese iron miners.
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Lack of association between cytokine gene polymorphisms and silicosis and pulmonary tuberculosis in Chinese iron miners.

机译:中国铁矿工中细胞因子基因多态性与矽肺和肺结核之间缺乏关联。

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摘要

Silicosis is a fibrotic lung disease produced by the inhalation and deposition of silica dust. The association between silicosis and pulmonary tuberculosis (PTB) has been well established. Cytokines participate in the development and progression of silicosis and PTB. Functional polymorphisms in cytokine genes have been identified that alter cytokine production. The aims of the current investigation were to determine whether functional polymorphisms in the tumor necrosis factor-alpha (TNF-alpha) gene at position -308; in the transforming growth factor-beta 1 (TGF-beta1) gene at positions -509, +869 (codon 10), and +915 (codon 25); in the interleukin-10 (IL-10) gene at position -1,082, -819 and -592; and in the intron 1 of the interferon-gamma (IFN-gamma) gene at position +874 are associated with silicosis and PTB. We conducted a case-control study with 183 silicosis patients and 111 silica-exposed miners, and a 1:2 matched case-control study of 61 PTB cases and 122 PTB-free miners. Genotype analysis wasperformed on genomic DNA, using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. There was complete linkage disequilibrium (LD) between the -819C and -592C alleles of the IL-10 gene. The genotype frequencies were similar between cases and control subjects for all investigated cytokine polymorphisms (p>0.05). We did not find an association between the different genotypes and severity of silicosis. We assume that these genetic variants do not play a dominant role in silicosis and PTB in our Chinese population.
机译:矽肺病是吸入和沉积矽尘产生的纤维化肺部疾病。矽肺病和肺结核(PTB)之间的关联已得到很好的建立。细胞因子参与矽肺病和PTB的发生和发展。已经确定了细胞因子基因中的功能多态性会改变细胞因子的产生。当前研究的目的是确定-308位肿瘤坏死因子-α(TNF-alpha)基因中的功能多态性是否存在。在-509,+ 869(密码子10)和+915(密码子25)位置的转化生长因子-beta 1(TGF-beta1)基因中;在白细胞介素10(IL-10)基因的-1,082,-819和-592位;干扰素-γ(IFN-γ)基因的内含子1中+874位与矽肺病和PTB有关。我们对183名矽肺病患者和111名接触二氧化硅的矿工进行了病例对照研究,并对61例PTB病例和122名无PTB矿工进行了1:2配对病例对照研究。使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析对基因组DNA进行基因型分析。 IL-10基因的-819C和-592C等位基因之间完全连锁不平衡(LD)。对于所有调查的细胞因子多态性,病例与对照组之间的基因型频率相似(p> 0.05)。我们没有发现不同基因型和矽肺病的严重程度之间的关联。我们假设这些遗传变异在我们中国人口的矽肺病和PTB中没有起主导作用。

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