Wang Huimin, Yang Guangzhi, Sun Dawei, Wang Boshen, Chen Hao, Chen Mengyao, Zhu Baoli
Key Laboratory of Environmental Medicine Engineering of Ministry of Education, School of Public Health, Southeast University, Nanjing, 210009, Jiangsu, China.
Institute of Occupational Disease Prevention, Jiangsu Province Center for Disease Prevention and Control, Nanjing, Jiangsu Province, China.
Environ Sci Pollut Res Int. 2021 Jul;28(28):38254-38262. doi: 10.1007/s11356-021-13486-5. Epub 2021 Mar 17.
Noise-induced hearing loss (NIHL) is one of these hazards which has been the second most common sensorineural hearing loss. Single-nucleotide polymorphisms (SNPs) mainly refer to the polymorphism of DNA sequence caused by the variation at the genomic nucleotide level. The influence of histone deacetylase 2 (HDAC2) variants on the risk of NIHL has not been studied. This research explored the association between HDAC2 and the development of NIHL. A total of 1146 industrial workers from one textile factory in east China were recruited to perform a case-control study. Basic clinical data such sex, age, smoking, and drinking was obtained by questionnaires; pure-toneaudiometry (PTA) tests were conducted by specialist physicians. Then, we performed genotyping of five selected SNPs (rs10499080, rs2475631, rs2499618, rs6568819, and rs3757016) in the HDAC2 gene in 600 NIHL patients and 546 controls. Finally, the main influences of the SNPs and their interactions with NIHL were assessed. Under the recessive model, there were statistically significant differences in the genotype frequencies of rs10499080 between two groups, and the results showed that individuals with rs10499080 CC+CT had a lower risk of NIHL (OR = 0.597, 95%CI = 0.357-0.998). Meanwhile, the significant difference in the genotype distributions between cases and controls was found in rs10499080 in the group with noise exposure of ≤ 16 years. But the following haplotype analysis showed that no association between all haplotypes in the HDAC2 gene and NIHL was been found. The genetic polymorphisms rs10499080 and rs6568819 within HDAC2 gene have an association with risk of NIHL. Workers exposed to noise with HDAC2 have a lower risk of NIHL.
噪声性听力损失(NIHL)是这些危害之一,它是第二常见的感音神经性听力损失。单核苷酸多态性(SNP)主要指基因组核苷酸水平变异导致的DNA序列多态性。组蛋白去乙酰化酶2(HDAC2)变体对NIHL风险的影响尚未得到研究。本研究探讨了HDAC2与NIHL发生之间的关联。招募了来自中国东部一家纺织厂的1146名产业工人进行病例对照研究。通过问卷获取性别、年龄、吸烟和饮酒等基本临床数据;由专科医生进行纯音听力测定(PTA)测试。然后,我们对600例NIHL患者和546名对照者的HDAC2基因中五个选定的SNP(rs10499080、rs2475631、rs2499618、rs6568819和rs3757016)进行基因分型。最后,评估了SNP的主要影响及其与NIHL的相互作用。在隐性模型下,两组之间rs10499080的基因型频率存在统计学显著差异,结果表明rs10499080 CC + CT个体患NIHL的风险较低(OR = 0.597,95%CI = 0.357 - 0.998)。同时,在噪声暴露≤16年的组中,rs10499080病例组和对照组之间的基因型分布存在显著差异。但随后的单倍型分析表明,未发现HDAC2基因中的所有单倍型与NIHL之间存在关联。HDAC2基因内的遗传多态性rs10499080和rs6568819与NIHL风险相关。暴露于噪声的工人携带HDAC2时患NIHL的风险较低。