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作 者:胡飞飞[1] 张恒东[2] 李昕[3] 卞倩[2] 朱宝立[2] 张正东[4]
机构地区:[1]常州市疾病预防控制中心,常州213022 [2]江苏省疾病预防控制中心 [3]南京市疾病预防控制中心 [4]南京医科大学公共卫生学院
出 处:《中华劳动卫生职业病杂志》2014年第2期104-107,共4页Chinese Journal of Industrial Hygiene and Occupational Diseases
基 金:江苏省自然科学基金资助项目(BK2010575);江苏省医学创新团队与领军人才项目(LJ201130)
摘 要:目的 探讨DNA甲基转移酶1基因(DNMT1) rs12984523、rs16999593和rs2228612单核苷酸多态性与中国汉族人群中噪声性听力损失(NIHL)易感性之间的关联.方法 采用病例-对照研究,电测听双耳高频平均听阈值≥40 dB为病例组,共188名工人;电测听结果双耳高频平均听阈值<40dB的300名工人为对照组.应用TaqMan探针法检测3个SNP位点的基因型.结果 DNMT1rs2228612携带TT基因型为NIHL的危险因素(调整后OR=1.69,95%CI:1.14~2.52).结论 在188例电测听双耳高频平均听阈值≥40 dB的中国汉族人群中,DNMT1 rs 2228612与噪声性听力损失的易感性有关.Objective To investigate the association between single nucleotide polymorphisms (SNPs) in DNA methyltransferase 1 (DNMT1) (rs12984523,rs16999593,and rs2228612) and noise-induced hearing loss (NIHL) in Chinese Han population.Methods This case-control study consisted of 188 cases (case group) and 300 controls (control group) in the same working position,who were matched for age and gender.The cases had a binaural average high-frequency hearing threshold not less than 40 dB,and the controls had a binaural average high-frequency heating threshold less than 40 dB.The genotypes at the three SNPs were determined by TaqMan probe.Results TT genotype at DNMT1 rs2228612 is a risk factor for NIHL (adjusted OR=1.69,95% CI:1.14-2.52).Conclusion The study of Chinese Han population suggested that DNMT1 rs2228612 is associated with susceptibility to NIHL.
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