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[钙黏蛋白CDH23基因多态性与中国工人噪声性听力损失的关联]

[Association of cadherin CDH23 gene polymorphisms with noise induced hearing loss in Chinese workers].

作者信息

Yang Miao, Tan Hao, Zheng Jian-Ru, Wang Feng, Jiang Changzheng, He Mei'an, Chen Yongwen, Wu Tangchun

机构信息

Institute of Occupational Medicine, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

Wei Sheng Yan Jiu. 2006 Jan;35(1):19-22.

Abstract

OBJECTIVE

To investigate the association of cadherin 23 gene (CDH23) polymorphisms with the development of noise induced hearing loss (NIHL).

METHODS

194 workers exposed to occupational noise were drawn as the subjects in the cross-sectional epidemiology study. According to the result of audiometry, they were divided into two groups: the NIHL group and the normal group. The genotypes of 93 workers with NIHL and 101 normal workers were tested by polymerase chain reaction followed by restriction fragment polymorphism analysis (PCR-RFLP).

RESULTS

There were no significant difference in the distribution of genotypes and alleles frequencies of the rs1227049 and rs1227051 positions between NIHL group and normal group (P > 0.05), there were significant differences between the two groups in the rs3802711 position and the terminal position of exon 7 (P < 0.01). After adjusted for age, sex, smoking, history of explosive noise exposure and cumulative noise exposure (CNE) with multiple logistic regression analysis, the risk of rs1227049 CC genotype was found significantly increased than that of the GG genotype, the OR value of which was 3.865 (95% CI 1.076 - 13.886), the risk of rs3802711 TT genotype was significantly higher than that of the CT genotype, the OR value of which was 6.088 (95% CI 2.485 - 14.917). GG genotype in the terminal position of exon 7 was also found a significantly higher risk than the AG genotype, the OR value of which was 5.769 (95% CI 2.745 - 12.121).

CONCLUSION

It was suggested that genetic polymorphism in cadherin CDH23 gene might play an important role in the development of NIHL in Chinese workers. The individuals with the rs1227049 CC genotype, rs3802711 TT genotype and GG genotype in the terminal position of exon 7 might be more susceptible to NIHL.

摘要

目的

探讨钙黏蛋白23基因(CDH23)多态性与噪声性听力损失(NIHL)发生发展的关系。

方法

选取194名职业性噪声暴露工人作为横断面流行病学研究对象。根据听力检测结果,将其分为两组:NIHL组和正常组。采用聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)检测93例NIHL工人和101例正常工人的基因型。

结果

NIHL组与正常组rs1227049和rs1227051位点的基因型和等位基因频率分布无显著差异(P>0.05),rs3802711位点和第7外显子末端位置两组间差异有统计学意义(P<0.01)。经年龄、性别、吸烟、爆震性噪声暴露史和累积噪声暴露(CNE)多因素logistic回归分析校正后,发现rs1227049 CC基因型的风险显著高于GG基因型,OR值为3.865(95%CI 1.076 - 13.886),rs3802711 TT基因型的风险显著高于CT基因型,OR值为6.088(95%CI 2.485 - 14.917)。第7外显子末端位置的GG基因型风险也显著高于AG基因型,OR值为5.769(95%CI 2.745 - 12.121)。

结论

提示钙黏蛋白CDH23基因多态性可能在中国工人NIHL发生发展中起重要作用。rs1227049 CC基因型、rs3802711 TT基因型和第7外显子末端位置的GG基因型个体可能更易患NIHL。

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