Variations in the Cadherin 23 Gene Associated With Noise-Induced Hearing Loss

References

• Mehrparvar AH, Mirmohammadi SJ, Hashemi SH, et al. Concurrent effect of noise exposure and smoking on extended high-frequency pure-tone thresholds. Int J Audiol. 2015;54(5):301–307. doi:10.3109/14992027.2014.978906
   PubMed Web of Science ®Google Scholar
• Upile T, Sipaul F, Jerjes W, et al. The acute effects of alcohol on auditory thresholds. BMC Ear Nose Throat Disord. 2007;7:4. doi:10.1186/1472-6815-7-4
   PubMedGoogle Scholar
• Taylor W, Pearson J, Mair A, Burns W. Study of noise and hearing in jute weaving. J Acoust Soc Am. 1965;38:113–120. doi:10.1002/ajhb.20744
   PubMed Web of Science ®Google Scholar
• Sliwinska-Kowalska M, Pawelczyk M. Contribution of genetic factors to noise-induced hearing loss: a human studies review. Mutat Res. 2013;752(1):61–65. doi:10.1016/j.mrrev.2012.11.001
   PubMed Web of Science ®Google Scholar
• Siemens J, Lillo C, Dumont RA, et al. Cadherin 23 is a component of the tip link in hair-cell stereocilia. Nature. 2004;428(6986):950–955. doi:10.1038/nature02483
   PubMed Web of Science ®Google Scholar
• Bouzid A, Smeti I, Chakroun A, et al. CDH23 methylation status and presbycusis risk in elderly women. Front Aging Neurosci. 2018;10:241. doi:10.3389/fnagi.2018.00241
   PubMed Web of Science ®Google Scholar
• Holme RH, Steel KP. Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation. J Assoc Res Otolaryngol. 2004;5(1):66–79. doi:10.1007/s10162-003-4021-2
   PubMed Web of Science ®Google Scholar
• Noben-Trauth K, Zheng QY, Johnson KR. Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet. 2003;35(1):21–23. doi:10.1038/ng1226
   PubMed Web of Science ®Google Scholar
• Davis RR, Newlander JK, Ling X, Cortopassi GA, Krieg EF, Erway LC. Genetic basis for susceptibility to noise-induced hearing loss in mice. Hear Res. 2001;155(1–2):82–90. doi:10.1016/s0378-5955(01)00250-7
   PubMed Web of Science ®Google Scholar
• Miyasaka Y, Shitara H, Suzuki S, et al. Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23. Hum Mol Genet. 2016;25(10):2045–2059. doi:10.1093/hmg/ddw078
   PubMed Web of Science ®Google Scholar
• Konings A, Van Laer L, Wiktorek-Smagur A, et al. Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populations. Ann Hum Genet. 2009;73(2):215–224. doi:10.1111/j.1469-1809.2008.00499.x
   PubMed Web of Science ®Google Scholar
• Yang M, Tan H, Zheng JR, et al. Association of cadherin CDH23 gene polymorphisms with noise induced hearing loss in Chinese workers. Wei Sheng Yan Jiu. 2006;35(1):19–22.
   PubMedGoogle Scholar
• Kowalski TJ, Pawelczyk M, Rajkowska E, Dudarewicz A, Sliwinska-Kowalska M. Genetic variants of CDH23 associated with noise-induced hearing loss. Otol Neurotol. 2014;35(2):358–365. doi:10.1097/MAO.0b013e3182a00332
   PubMed Web of Science ®Google Scholar
• Xu X, Yang Q, Jiao J, et al. Genetic variation in POU4F3 and GRHL2 associated with noise-induced hearing loss in Chinese population: a case-control study. Int J Environ Res Public Health. 2016;13(6):561. doi:10.3390/ijerph13060561
   PubMed Web of Science ®Google Scholar
• National Health and Family Planning Commission of the PRC. Diagnosis of occupational noise deafness (instead of GBZ 49-2007). Available fromhttp://www.nhc.gov.cn/zwgkzt/pyl/201410/12e4ec65af8e46248bb45d366a0d5021.shtml. Accessed March 20, 2024.
   Google Scholar
• National Health and Family Planning Commission of the PRC. Measurement of physical factors in the workplace -Part 8: noise. Available fromhttp://www.nhc.gov.cn/zwgkzt/pyl/201410/1a150c9e20f846b8a651d2fd69c6bdb0.shtmlAccessed March 20, 2024.
   Google Scholar
• Xie HW, Qiu W, Heyer NJ, et al. The use of the kurtosis-adjusted cumulative noise exposure metric in evaluating the hearing loss risk for complex noise. Ear Hear. 2016;37(3):312–323. doi:10.1097/AUD.0000000000000251
   PubMed Web of Science ®Google Scholar
• Ting JC, Ye Y, Thomas GH, Ruczinski I, Pevsner J. Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan. BMC Bioinf. 2006;7:25. doi:10.1186/1471-2105-7-25
   PubMed Web of Science ®Google Scholar
• Abbasi M, Pourrajab B, Tokhi MO. Protective effects of vitamins/antioxidants on occupational noise-induced hearing loss: a systematic review. J Occup Health. 2021;63(1):e12217. doi:10.1002/1348-9585.12217
   PubMed Web of Science ®Google Scholar
• Henderson D, Bielefeld EC, Harris KC, Hu BH. The role of oxidative stress in noise‐induced hearing loss. Ear Hear. 2006;27(1):1–19. doi:10.1097/01.aud.0000191942.36672.f3
   PubMed Web of Science ®Google Scholar
• Quaranta N, Dicorato A, Matera V, D’Elia A, Quaranta A. The effect of alpha‐lipoic acid on temporary threshold shift in humans: a preliminary study. Acta Otorhinolaryngol Ital. 2012;32:380–385.
   PubMed Web of Science ®Google Scholar
• Yang M, Tan H, Yang Q, et al. Association of hsp70 polymorphisms with risk of noise-induced hearing loss in Chinese automobile workers. Cell Stress Chaperones. 2006;11(3):233–239. doi:10.1111/j.1469-1809.2008.00499.x
   PubMed Web of Science ®Google Scholar
• Konings A, Van Laer L, Michel S, et al. Variations in HSP70 genes associated with noise-induced hearing loss in two independent populations. Eur J Hum Genet. 2009;17(3):329–335. doi:10.1038/ejhg.2008.172
   PubMed Web of Science ®Google Scholar
• Qian PY, Zhao ZX, Liu SY, et al. Alcohol as a risk factor for hearing loss: a systematic review and meta-analysis. PLoS One. 2023;18(1):e0280641. doi:10.1371/journal.pone.0280641
   PubMed Web of Science ®Google Scholar
• Jiang Z, Fa B, Zhang X, et al. Identifying genetic risk variants associated with noise-induced hearing loss using a novel strategy for evaluating individual susceptibility. Hear Res. 2021;407:108281. doi:10.1016/j.heares.2021.108281
   PubMed Web of Science ®Google Scholar
• Sliwinska-Kowalska M, Noben-Trauth K, Pawelczyk M, Kowalski TJ. Single nucleotide polymorphisms in the cadherin 23 (CDH23) gene in polish workers exposed to industrial noise. Am J Hum Biol. 2008;20(4):481–483. doi:10.1002/ajhb.20744
   PubMed Web of Science ®Google Scholar
• Jiang CM. Single nucleotide polymerase in CDH23, PMCA2 gene in workers exposed to industrial noise. Master’s Deg Thesis Guangdong Pharmaceutical University. 2012.
   Google Scholar
• Zheng QY, Yan D, Ouyang XM, et al. Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans. Hum Mol Genet. 2005;14(1):103–111. doi:10.1093/hmg/ddi010
   PubMed Web of Science ®Google Scholar
• Kazmierczak P, Sakaguchi H, Tokita J, et al. Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells. Nature. 2007;449(7158):87–91. doi:10.1038/nature06091
   PubMed Web of Science ®Google Scholar
• Muller U. Cadherins and mechanotransduction by hair cells. Curr Opin Cell Biol. 2008;20(5):557–566. doi:10.1016/j.ceb.2008.06.004
   PubMed Web of Science ®Google Scholar
• Sakaguchi H, Tokita J, Müller U, Kachar B. Tip links in hair cells: molecular composition and role in hearing loss. Curr Opin Otolaryngol Head Neck Surg. 2009;17(5):388–393. doi:10.1097/MOO.0b013e3283303472
   PubMed Web of Science ®Google Scholar
• Wang SL, Yu LG, Liu RP, et al. Gene-gene interaction of GJB2, SOD2, and CAT on occupational noise-induced hearing loss in Chinese han population. Biomed Environ Sci. 2014;27(12):965–968. doi:10.3967/bes2014.131
   PubMed Web of Science ®Google Scholar
• Lie A, Skogstad M, Johannessen HA, et al. Occupational noise exposure and hearing: a systematic review. Int Arch Occup Environ Health. 2016;89(3):351–372. doi:10.1007/s00420-015-1083-5
   PubMed Web of Science ®Google Scholar
• Jiao J, Gu GZ, Chen GS, et al. Relationship research among CDH23 gene and the risk of noise-induced hearing loss. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2020;38(2):84–90. doi:10.3760/cma.j.issn.1001-9391.2020.02.002
   PubMedGoogle Scholar