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Effect of GRM7 polymorphisms on the development of noise-induced hearing loss in Chinese Han workers: a nested case-control study

机译:GRM7基因多态性对中国汉族工人噪声诱发的听力损失发展的影响:嵌套的病例对照研究。

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摘要

BackgroundNoise-induced hearing loss (NIHL) is a complex, irreversible disease caused by the interaction of genetic and environmental factors. In recent years, a great many studies have been done to explore the NIHL susceptibility genes among humans. So far, high powerful detections have been founded that genes of potassium ion channel genes (KCNQ4 and KCNE1), catalase (CAT), protocadherin 15 (PCDH15), myosin 14 (MYH14) and heart shock protein (HSP70) which have been identified in more than one population may be associated with the susceptibility to NIHL. As for metabolic glutamate receptor7 gene (GRM7), a lot of researches mainly focus on age-related hearing loss (ARHL) and the results have shown that the polymorphisms of GRM7 are linked to the development of ARHL. However, little is known about the association of GRM7 and the susceptibility to NIHL. Therefore, the aim of this study was to explore the effect of GRM7 polymorphisms on the susceptibility to NIHL.
机译:背景噪声诱发的听力损失(NIHL)是一种复杂的,不可逆的疾病,由遗传和环境因素的相互作用引起。近年来,已经进行了许多研究来探索人类中NIHL的易感基因。迄今为止,已经建立了强大的检测手段,已在以下人群中鉴定出了钾离子通道基因(KCNQ4和KCNE1),过氧化氢酶(CAT),原钙粘蛋白15(PCDH15),肌球蛋白14(MYH14)和心跳蛋白(HSP70)。一个以上的人群可能与NIHL的易感性有关。关于代谢性谷氨酸受体7基因(GRM7),许多研究主要集中在与年龄有关的听力损失(ARHL)上,结果表明GRM7的多态性与ARHL的发生有关。但是,关于GRM7与NIHL的易感性知之甚少。因此,本研究的目的是探讨GRM7多态性对NIHL易感性的影响。

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