Associations of GST Gene Polymorphisms and GST Enzyme Activity with the Development of Noise-Induced Hearing Loss in Chinese Han Males.

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY Public Health Genomics Pub Date : 2024-01-01 Epub Date: 2024-10-30 DOI:10.1159/000541618
Fang Ji, Jian Zhang, Xiaowen Ding, Li Rong, Xiaodong Liu, Tenglong Yan, Jue Li
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Abstract

Introduction: In noise-induced hearing loss (NIHL), glutathione S-transferases (GSTs) play a pivotal role as antioxidants in cochlear protection. Nevertheless, the variability in population and environmental factors complicates the interpretation of research findings on the association among GST gene polymorphism, GST enzyme activity, and NIHL, leading to inconsistent results. To explore the potential correlation between them, we took a cross-sectional survey.

Methods: For workers with NIHL, standard 1:1 propensity score matching was applied to create a highly comparable control group. Multiplex PCR was used to detect GSTT1 and GSTM1 gene deletions, PCR-restriction fragment length polymorphism was used to detect the GSTP1 rs1695 gene polymorphism, and a GST assay kit was used to measure total plasma GST activity. Furthermore, we analyzed the relationship among GST gene polymorphism, GST enzyme activity, and NIHL.

Results: This study included 144 workers with NIHL and 144 workers with normal hearing. The GSTM1 null genotype was significantly higher among workers with NIHL than controls (64.6% vs. 49.3%), regression analysis revealed a significant correlation between GSTM1 null genotype and elevated susceptibility to NIHL (p = 0.013). Workers with NIHL had significantly lower GST activity than healthy controls (p < 0.05). GST enzymes were not affected by GSTT1, GSTM1, or GSTP1 polymorphisms.

Conclusion: GSTM1 null genotype but not GSTM1 alone may confer susceptibility to NIHL, and serum GST enzyme activity is linked to NIHL.

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中国汉族男性 GST 基因多态性和 GST 酶活性与噪声性听力损失发病的关系
引言 在噪声性听力损失(NIHL)中,谷胱甘肽 S 转移酶(GST)作为抗氧化剂在保护耳蜗方面发挥着关键作用。然而,由于人群和环境因素的差异,有关 GST 基因多态性、GST 酶活性和 NIHL 之间相关性的研究结果解释变得复杂,导致结果不一致。为了探讨它们之间的潜在相关性,我们进行了一项横断面调查。方法 对于患有 NIHL 的工人,采用标准的 1:1 倾向得分匹配法来创建一个高度可比的对照组。使用多重 PCR 检测 GSTT1 和 GSTM1 基因缺失,使用 PCR-RFLP 检测 GSTP1 rs1695 基因多态性,使用 GST 检测试剂盒测定血浆总 GST 活性。此外,我们还分析了 GST 基因多态性、GST 酶活性和 NIHL 之间的关系。结果 本研究包括 144 名患有 NIHL 的工人和 144 名听力正常的工人。在 NIHL 患者中,GSTM1 空基因型明显高于对照组(64.6% 对 49.3%),回归分析显示 GSTM1 空基因型与 NIHL 易感性升高之间存在显著相关性(P=0.013)。患有 NIHL 的工人的 GST 活性明显低于健康对照组(p=0.013)。
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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
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