100
Views
4
CrossRef citations to date
0
Altmetric
Original

Genetic factors in noise induced hearing loss

, &
Pages 25-32 | Published online: 11 Jul 2009

References

  • Gates GA, Couropmitree NN, Myers RH. Genetic associations in age-related hearing thresholds. Arch Otolaryngol Head Neck Surg. 1999; 125: 654–9
  • Davis RR, Kozel P, Erway LC. Genetic influences in individual susceptibility to noise: a review. Noise Health. 2003; 5: 19–28
  • Henry KR. Influence of genotype and age on noise-induced auditory losses. Behav Genet. 1982; 12: 563–73
  • Ohlemiller KK. Contributions of mouse models to understanding of age- and noise-related hearing loss. Brain Res. 2006; 26: 89–102
  • Chen TJ, Chen SS, Wang DC, Hsieh YL. Increased vulnerability of auditory system to noise exposure in mdx mice. Laryngoscope. 2002; 112: 520–5
  • Schick B, Praetorius M, Eigenthaler M, Jung V, Muller M, Walter U, et al. Increased noise sensitivity and altered inner ear MENA distribution in VASP-/- mice. Cell Tissue Res. 2004; 318: 493–502
  • Fairfield DA, Lomax MI, Dootz GA, Chen S, Galecki AT, Benjamin IJ, et al. Heat shock factor 1-deficient mice exhibit decreased recovery of hearing following noise overstimulation. J Neurosci Res. 2005; 81: 589–96
  • Sugahara K, Inouye S, Izu H, Katoh Y, Katsuki K, Takemoto T, et al. Heat shock transcription factor HSF1 is required for survival of sensory hair cells against acoustic overexposure. Hear Res. 2003; 182: 88–96
  • Johnson KR, Erway LC, Cook SA, Willott JF, Zheng QY. A major gene affecting age-related hearing loss in C57BL/6J mice. Hear Res. 1997; 114: 83–92
  • Johnson KR, Zheng QY, Erway LC. A major gene affecting age-related hearing loss is common to at least 10 inbred strains of mice. Genomics. 2000; 70: 171–80
  • Erway LC, Shiau YW, Davis RR, Krieg EF. Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss. Hear Res. 1996; 93: 181–7
  • 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: 82–90
  • 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: 66–79
  • Kozel PJ, Davis RR, Krieg EF, Shull GE, Erway LC. Deficiency in plasma membrane calcium ATPase isoform 2 increases susceptibility to noise-induced hearing loss in mice. Hear Res. 2002; 164: 231–9
  • McFadden SL, Ding D, Reaume AG, Flood DG, Salvi RJ. Age-related cochlear hair cell loss is enhanced in mice lacking copper/zinc superoxide dismutase. Neurobiol Aging. 1999; 20: 1–8
  • Ohlemiller KK, McFadden SL, Ding DL, Flood DG, Reaume AG, Hoffman EK, et al. Targeted deletion of the cytosolic Cu/Zn-superoxide dismutase gene (SOD1) increases susceptibility to noise-induced hearing loss. Audiol Neurootol. 1999; 4: 237–46
  • Ohlemiller KK, Wright JS, Dugan LL. Early elevation of cochlear reactive oxygen species following noise exposure. Audiol Neurootol. 1999; 4: 229–36
  • Keithley EM, Canto C, Zheng QY, Wang X, Fischel-Ghodsian N, Johnson KR. Cu/Zn superoxide dismutase and age-related hearing loss. Hear Res. 2005; 209: 76–85
  • Ohlemiller KK, McFadden SL, Ding DL, Lear PM, Ho YS. Targeted mutation of the gene for cellular glutathione peroxidase (Gpx1) increases noise-induced hearing loss in mice. J Assoc Res Otolaryngol 2000a; 1: 243–54
  • Ohlemiller KK, Wright JS, Heidbreder AF. Vulnerability to noise-induced hearing loss in ‘middle-aged’ and young adult mice: a dose-response approach in CBA, C57BL, and BALB inbred strains. Hear Res 2000; 149: 239–47
  • Tabuchi K, Suzuki M, Mizuno A, Hara A. Hearing impairment in TRPV4 knockout mice. Neurosci Lett. 2005; 382: 304–8
  • Ohlemiller KK, Gagnon PM. Genetic impairment of ceruloplasmin, an iron regulatory protein, promotes noise-induced hearing loss (NIHL) and age-related hearing loss (ARHL). 2005 Abstr Ass Res Otolaryngol. 2005; 28: 199
  • Yoshida N, Hequembourg SJ, Atencio CA, Rosowski JJ, Liberman MC. Acoustic injury in mice: 129/SvEv is exceptionally resistant to noise-induced hearing loss. Hear Res. 2000; 141: 97–106
  • Candreia C, Martin GK, Stagner BB, Lonsbury-Martin BL. Distortion product otoacoustic emissions show exceptional resistance to noise exposure in MOLF/Ei mice. Hear Res. 2004; 194: 109–17
  • Vazquez AE, Jimenez AM, Martin GK, Luebke AE, Lonsbury-Martin BL. Evaluating cochlear function and the effects of noise exposure in the B6.CAST + Ahl mouse with distortion product otoacoustic emissions. Hear Res. 2004; 194: 87–96
  • Erway LC, Willot JF, Archer JR, Harrison DE. Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains. Hear Res. 1993; 65: 125–32
  • Davis RR, Cheever ML, Krieg EF, Erway LC. Quantitative measure of genetic susceptibility to noise-induced hearing loss in two strains of mice. Hear Res. 1999; 134: 9–15
  • Noben-Trauth K, Zheng QY, Johnson KR, Nishina PM. mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics. 1997; 44: 266–72
  • Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B, et al. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nat Genet. 2001; 27: 103–7
  • Pickles JO, Brix J, Comis SD, Gleich O, Koppl C, Manley GA, et al. The organization of tip links and stereocilia on hair cells of bird and lizard basilar papillae. Hear Res. 1989; 41: 31–42
  • Fridberger A, Flock A, Ulfendahl M, Flock B. Acoustic overstimulation increases outer hair cell Ca2 +  concentrations and causes dynamic contractions of the hearing organ. Proc Natl Acad Sci. U S A 1998; 95: 7127–32
  • Kozel PJ, Friedman RA, Erway LC, Yamoah EN, Liu LH, Riddle T, et al. Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2 + -ATPase isoform 2. J Biol Chem. 1998; 273: 18693–6
  • Street VA, McKee-Johnson JW, Fonseca RC, Tempel BL, Noben-Trauth K. Mutations in a plasma membrane Ca2 + -ATPase gene cause deafness in deafwaddler mice. Nat Genet. 1998; 19: 390–4
  • Bryda EC, Kim HJ, Legare ME, Frankel WN, Noben-Trauth K. High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (Cdh23v). Genomics. 2001; 73: 338–42
  • Noben-Trauth K, Zheng QY, Johnson KR. Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nature Genet. 2003; 35: 21–3
  • Harding GW, Bohne BA, Vos JD. The effect of an age-related hearing loss gene (Ahl) on noise-induced hearing loss and cochlear damage from low-frequency noise. Hear Res. 2005; 204: 90–100
  • Hirose K, Discolo CM, Keasler JR, Ransohoff R. Mononuclear phagocytes migrate into the murine cochlea after acoustic trauma. J Comp Neurol. 2005; 489: 180–94
  • Bärrenas M, Lindgren F. The influence of eye colour on susceptibility to TTS in humans. Br J Audiol. 1991; 25: 203–207
  • Bärrenas M. Pigmentation and noise-induced hearing loss: is the relationship between pigmentation and noise-induced hearing loss due to an ototoxic pheolamin interaction or to otoprotective eumelan effects. In Prasher D, Luxon L, editors. Advances in Noise Research. Vol 1. Biological effect of noise. London: Whurr; 1998. p. 59–70.
  • Voisey J, van Daal A. Agouti: from mouse to man, from skin to fat. Pigment Cell Res. 2002; 15: 10–8
  • Picciotti PM, Torsello A, Cantore I, Stigliano E, Paludetti G, Wolf FI. Expression of vascular endothelial growth factor and its receptors in the cochlea of various experimental animals. Acta Otolaryngol. 2005; 125: 1152–7
  • Lamm K, Arnold W. The effect of blood flow promoting drugs on cochlear blood flow, perilymphatic pO(2) and auditory function in the normal and noise-damaged hypoxic and ischaemic guinea pig inner ear. Hear Res. 2000; 141: 199–219
  • Yang M, Tan H, Zheng JR, Wang F, Jiang C, He M, et al. Association of cadherin CDH23 gene polymorphisms with noise induced hearing loss in Chinese workers. Wei Sheng Yan Jiu 2006; 35: 19–22
  • van Laer L, Carlsson PI, Ottschytsch N, Bondeson ML, Konings A, Vandevelde A, et al. The contribution of genes involved in potassium recycling in the inner ear to noise-induced hearing loss. Hum Mutat. 2006; 27: 786–95
  • Malczyk-Pawelczyk M, van Laer L, van Camp G, Rajkowska E, Dudarewicz A, Sliwinska-Kowalska M. Association of variation in potassium recycling pathway genes and noise-induced hearing loss in a Polish noise-exposed population. Proceedings of the XXVIIIth International Congress of Audiology, ICAud2006, September 3–7, 2006, Innsbruck, Austria.
  • Fortunato G, Marciano E, Zarrilli F, Mazzaccara C, Intrieri M, Calcagno G, et al. Paraoxonase and superoxide dismutase gene polymorphisms and noise-induced hearing loss. Clin Chem. 2004; 50: 2012–8
  • Carlsson PI, van Laer L, Borg E, Bondeson ML, Thys M, Fransen E, et al. The influence of genetic variation in oxidative stress genes on human noise susceptibility. Hear Res. 2005; 202: 87–96
  • Corbacella E, Lanzoni I, Bertolaso L, Previati M, Martini A. Protective effects of minocycline and MDL 28170 in gentamicin ototoxicity. Aud Med. (in press).
  • Jacobs HT, Hutchin TP, Kappi T, Gillies G, Minkkinen K, Walker J, et al. Mitochondrial DNA mutations in patients with postlingual, non-syndromic hearing impairment. Eur J Hum Genet. 2005; 13: 26–33
  • Nadeau JH. Listening to genetic background noise. N Engl J Med. 2005; 352: 1598–9
  • Martini A, Prosser S. Genetics of noise- induced hearing loss In: Farinella B, editor. The audiological picture of occupational deafness from noise. Vol II. Palermo: Medical Books; 2004. p. 47–57.
  • Coucke P, van Camp G, Djoyodiharjo B, Smith SD, Frants RR, Padberg GW, et al. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. N Engl J Med. 1994; 331: 425–31
  • Robertson NG, Lu L, Heller S, Merchant SN, Eavey RD, McKenna M, et al. Mutations in a novel cochlear gene cause DFNA9, a human non-syndromic deafness with vestibular dysfunction. Nat Genet. 1998; 20: 299–303
  • Manolis EN, Yandavi N, Nadol JB, Jr, Eavey RD, McKenna M, Rosenbaum S, et al. A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12–13. Hum Mol Genet. 1996; 5: 1047–50
  • Wayne S, Robertson NG, DeClau F, Chen N, Verhoeven K, Prasad S, et al. Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus. Hum Mol Genet. 2001; 10: 195–200
  • O'Neill ME, Marietta J, Nishimura D, Wayne S, van Camp G, van Laer L, et al. A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6. Hum Mol Genet. 1996; 5: 853–6
  • Lalwani AK, Luxford WM, Mhatre AN, Attaie A, Wilcox ER, Castelein CM. A new locus for non-syndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration. Am J Hum Genet. 1999; 64: 318–23
  • Elfenbein JL, Fisher RA, Wei S, Morell RJ, Stewart C, Friedman TB, et al. Audiological aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss. Ear Hear. 2001; 22: 279–88
  • Greene CC, McMillan PM, Barker SE, Kurnool P, Lomax MI, Burmeister M, et al. DFNA25, a novel locus for dominant non-syndromic hereditary hearing impairment, maps to 12q21–24. Am J Hum Genet. 2001; 68: 254–60
  • Xiao S, Yu C, Chou X, Yuan W, Wang Y, Bu L, et al. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat Genet. 2001; 27: 201–4
  • 2003/10/EC Council directive on the minimum health and safety requirements regarding the exposure of workers to the risks arising from physical agents (noise), European Commission, Brussels, 2003.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.