Jiao J, Yuan L L, Li T, Wu H, Gu G Z, Chen G S, Zhang H L, Yu S F
Department of Occupational Health, The Third People's Hospital of Henan Province (Henan Hospital for Occupational Diseases),Zhengzhou 450052, China.
Department of Occupational Health,School of Public Health, Zhengzhou University, Zhengzhou 450001, China.
Zhonghua Yu Fang Yi Xue Za Zhi. 2022 Aug 6;56(8):1087-1094. doi: 10.3760/cma.j.cn112150-20210917-00905.
To explore the relationship between DNA methylation and occupational noise-induced hearing loss. A case-control study was conducted. People with hearing loss induced by occupational noise were recruited as the case group and those with normal hearing but still exposed to occupational noise were recruited as the control group. A total of 60 participants were included, of which 30 participants were in the case group and 30 in the control group. The methylation level was detected by 850k genome-wide DNA methylation chip technology. The significance of differential methylated position (DMP) was tested by R-packet 'Champ'. The differential methylated region (DMR) was analyzed by using Champ's Bumphunter algorithm. Cluster profiler was used to analyze the gene list for GO and KEGG pathway enrichment. There was significant difference between two groups in binaural high-frequency average hearing threshold (<0.05), but there was no significant difference in age, smoking, drinking, hypertension, physical exercise and cumulative noise exposure. The results of DMP and DMR analysis showed that 713875 sites were detected in the case group and the control group, and 439 methylation sites with significant difference, accounting for 0.06%; 650 regions were detected, and 72 methylation regions with significant differences, accounting for 11.08%. Compared with the control group, the results of GO enrichment analysis showed that the case group had statistically significant differences in four pathways: axogenesis of projection neurons in the central nervous system, neuronal development in the central nervous system, axogenesis of neurons in the central nervous system and neuronal differentiation in the central nervous system. KEGG enrichment analysis showed that there were significant differences in sphingolipid metabolism, aldosterone synthesis and secretion, primary bile acid biosynthesis pathway between the case group and the control group. The occurrence of occupational noise-induced hearing loss may be related to the regulation of gene expression related to axogenesis of projection neurons in the central nervous system, development of neurons in the central nervous system, axogenesis of neurons in the central nervous system, differentiation of neurons in the central nervous system, sphingolipid metabolism, aldosterone synthesis and secretion, primary bile acid biosynthesis and gene methylation related to metabolism.
为探讨DNA甲基化与职业性噪声性听力损失之间的关系。进行了一项病例对照研究。将职业性噪声所致听力损失者招募为病例组,将听力正常但仍暴露于职业性噪声者招募为对照组。共纳入60名参与者,其中病例组30名,对照组30名。采用850k全基因组DNA甲基化芯片技术检测甲基化水平。用R包“Champ”检验差异甲基化位点(DMP)的显著性。采用Champ的Bumphunter算法分析差异甲基化区域(DMR)。使用Cluster profiler分析基因列表进行GO和KEGG通路富集分析。两组双耳高频平均听阈差异有统计学意义(<0.05),但年龄、吸烟、饮酒、高血压、体育锻炼和累积噪声暴露方面差异无统计学意义。DMP和DMR分析结果显示,病例组和对照组共检测到713875个位点,其中差异有统计学意义的甲基化位点439个,占0.06%;检测到650个区域,其中差异有统计学意义的甲基化区域72个,占11.08%。与对照组相比,GO富集分析结果显示,病例组在中枢神经系统投射神经元轴突发生、中枢神经系统神经元发育、中枢神经系统神经元轴突发生、中枢神经系统神经元分化这四条通路中差异有统计学意义。KEGG富集分析显示,病例组与对照组在鞘脂代谢、醛固酮合成与分泌、初级胆汁酸生物合成途径方面存在显著差异。职业性噪声性听力损失的发生可能与中枢神经系统投射神经元轴突发生、中枢神经系统神经元发育、中枢神经系统神经元轴突发生、中枢神经系统神经元分化、鞘脂代谢、醛固酮合成与分泌、初级胆汁酸生物合成以及与代谢相关的基因甲基化对基因表达的调控有关。