• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[基于队列研究的KCNQ4基因多态性对噪声性听力损失风险随CNE或噪声暴露持续时间变化的预测——Cox模型分析]

[Prediction of KCNQ4gene polymorphism varies with CNE or noise exposure duration on the Risk of NIHL-Cox model analysis based on cohort study].

作者信息

Zhou W H, Gu G Z, Wu H, Li Y H, Chen G S, Zhang H L, Yu S F, Zheng Y X

机构信息

Henan Provincial Institute for Occupational Health, Zhengzhou 450052, China.

Wugang Institute for Occupational Health, Wugang 462599, China.

出版信息

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2020 Feb 20;38(2):111-116. doi: 10.3760/cma.j.issn.1001-9391.2020.02.007.

DOI:10.3760/cma.j.issn.1001-9391.2020.02.007
PMID:32306673
Abstract

The purpose of this study was to explore the association between gene in the potassium recycling pathway 4 (KCNQ4) polymorphisms and the susceptibility to noise-induced hearing loss (NIHL) , and analysis the effect of cumulative noise exposure (CNE) and noise exposure duration on this association. A nested case-control study with 1∶1 matched was used based on the cohort of noise exposure in a steel factory. A total of 286 cases were selected as the group of hearing loss and 286 controls were chosen according to the matching standards of same gender, same type of work, age difference ≤ 5 years, noise exposure duration ≤ 2 years. The single nucleotide polymorphisms (SNPs) of rs4660468, rs4660470, rs34287852 in KCNQ4 were genotyped by SNPscan(TM) method. The codominant, dominant and recessive models were established to study KCNQ4 polymorphisms and the susceptibility to NIHL by single-factor conditional logistic regression analysis. The COX regression analysis was used to analyze the risk of developing NIHL in individuals with different genotypes along with the extending of noise exposure duration or CNE. In the case of CNE≤96 dB (A) ·year, the risk of developing NIHL in individuals with TA genotype of rs4660470 was 2.197 times than individuals with TT genotypes (95%: 1.0324.677) , and those with TA+AA and TT genotypes (HR=2.467, 95%: 1.0255.934) With the increase of noise exposure duration, in rs4660470, individuals with TA genotype had a higher risk of suffering NIHL than those with TT genotype (HR=1.461, 95%: 1.061~2.011) , individuals with TA and/or AA genotype had a earlier risk of suffering NIHL than those with TT genotype. The mutant allele A of rs4660470 in KCNQ4 may be a risk factor for developing NIHL, CNE≤100 dB (A) ·year or the increase of noise exposure duration may further increase the risk of NIHL.

摘要

本研究旨在探讨钾离子循环通路4(KCNQ4)基因多态性与噪声性听力损失(NIHL)易感性之间的关联,并分析累积噪声暴露(CNE)和噪声暴露持续时间对这种关联的影响。基于某钢铁厂噪声暴露队列,采用1∶1匹配的巢式病例对照研究。共选取286例听力损失患者作为病例组,按照性别相同、工作类型相同、年龄相差≤5岁、噪声暴露持续时间≤2年的匹配标准选取286例对照。采用SNPscan(TM)方法对KCNQ4基因的rs4660468、rs4660470、rs34287852单核苷酸多态性(SNP)进行基因分型。通过单因素条件logistic回归分析建立共显性、显性和隐性模型,研究KCNQ4基因多态性与NIHL易感性的关系。采用COX回归分析,分析不同基因型个体随着噪声暴露持续时间延长或CNE增加发生NIHL的风险。在CNE≤96 dB(A)·年的情况下,rs4660470基因TA基因型个体发生NIHL的风险是TT基因型个体的2.197倍(95%:1.0324.677),TA+AA基因型个体与TT基因型个体相比(HR=2.467,95%:1.0255.934)。随着噪声暴露持续时间增加,在rs4660470基因中,TA基因型个体发生NIHL的风险高于TT基因型个体(HR=1.461,95%:1.061~2.011),TA和/或AA基因型个体发生NIHL的风险早于TT基因型个体。KCNQ4基因rs4660470的突变等位基因A可能是发生NIHL的危险因素,CNE≤100 dB(A)·年或噪声暴露持续时间增加可能会进一步增加NIHL的风险。

相似文献

1
[Prediction of KCNQ4gene polymorphism varies with CNE or noise exposure duration on the Risk of NIHL-Cox model analysis based on cohort study].[基于队列研究的KCNQ4基因多态性对噪声性听力损失风险随CNE或噪声暴露持续时间变化的预测——Cox模型分析]
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2020 Feb 20;38(2):111-116. doi: 10.3760/cma.j.issn.1001-9391.2020.02.007.
2
[Association between GSTP1 gene polymorphisms and susceptibility to noise-induced hearing loss].谷胱甘肽S-转移酶P1基因多态性与噪声性听力损失易感性的关联
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2020 Feb 20;38(2):101-107. doi: 10.3760/cma.j.issn.1001-9391.2020.02.005.
3
[Relationship research among CDH23 gene and the risk of noise-induced hearing loss].[CDH23基因与噪声性听力损失风险的关系研究]
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2020 Feb 20;38(2):84-90. doi: 10.3760/cma.j.issn.1001-9391.2020.02.002.
4
[Investigation into the relationship between mitochondrial 12 S rRNA gene, tRNA gene and cytochrome oxidase Ⅱ gene variations and the risk of noise-induced hearing loss].[线粒体12S rRNA基因、tRNA基因及细胞色素氧化酶Ⅱ基因变异与噪声性听力损失风险的关系研究]
Zhonghua Yu Fang Yi Xue Za Zhi. 2017 Jan 6;51(1):34-40. doi: 10.3760/cma.j.issn.0253-9624.2017.01.008.
5
[Association between variations in protocadherin 15 gene and occupational noise-induced hearing loss].[原钙黏蛋白15基因变异与职业性噪声性听力损失之间的关联]
Zhonghua Yu Fang Yi Xue Za Zhi. 2017 Jan 6;51(1):20-26. doi: 10.3760/cma.j.issn.0253-9624.2017.01.006.
6
Genetic variation in KCNQ4 gene is associated with susceptibility to noise-induced hearing loss in a Chinese population.KCNQ4 基因的遗传变异与中国人群噪声性听力损失的易感性相关。
Environ Toxicol Pharmacol. 2018 Oct;63:55-59. doi: 10.1016/j.etap.2018.08.009. Epub 2018 Aug 17.
7
[Association between eye absent homolog 4 gene polymorphisms and occupational noise-induced hearing loss].眼缺失同源物4基因多态性与职业性噪声性听力损失之间的关联
Zhonghua Yu Fang Yi Xue Za Zhi. 2017 Jan 6;51(1):27-33. doi: 10.3760/cma.j.issn.0253-9624.2017.01.007.
8
[Association between GSTP1 gave polymorphisms and susceptibility to noise-induced hearing loss].[谷胱甘肽S-转移酶P1基因多态性与噪声性听力损失易感性的关联]
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2020 Feb 20;38(2):120-124. doi: 10.3760/cma.j.issn.1001-9391.2020.02.009.
9
Effect of GRM7 polymorphisms on the development of noise-induced hearing loss in Chinese Han workers: a nested case-control study.GRM7基因多态性对中国汉族工人噪声性听力损失发生发展的影响:一项巢式病例对照研究
BMC Med Genet. 2018 Jan 5;19(1):4. doi: 10.1186/s12881-017-0515-3.
10
[Relationship between GRM7 gene polymorphisms and the susceptbility to noise-induced hearing loss].GRM7基因多态性与噪声性听力损失易感性的关系
Wei Sheng Yan Jiu. 2018 Mar;47(2):218-227.

引用本文的文献

1
[Research progress in genetics of noise-induced hearing loss].[噪声性听力损失的遗传学研究进展]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 Apr;38(4):343-347;353. doi: 10.13201/j.issn.2096-7993.2024.04.016.
2
The Role of Genetic Variants in the Susceptibility of Noise-Induced Hearing Loss.基因变异在噪声性听力损失易感性中的作用。
Front Cell Neurosci. 2022 Jul 12;16:946206. doi: 10.3389/fncel.2022.946206. eCollection 2022.