79
Views
11
CrossRef citations to date
0
Altmetric
Original

The influence of genetic factors, smoking and cardiovascular diseases on human noise susceptibility

, , &
Pages 82-91 | Published online: 11 Jul 2009

References

  • Calvo J, Rabionet R, Gasparini P, Estivill X. Connexins and deafness Homepage. World wide web (homepage on the Internet) (cited 2004 April 13). Available from: http://www.crg.es/deafness.
  • McGuirt WT, Smith R J. Connexin 26 as a cause of hereditary hearing loss. Am J Audiol. 1999; 8: 93–100
  • van Laer L, van Camp G.Genes in the ear: what have we learned over the last years? Scand Audiol Suppl. 2001:44–53.
  • Morton N E. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci. 1991; 630: 16–31
  • Kelsell DP, Dunlop J, Stevens HP, Lench NJ, Liang JN, Parry G, et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature. 1997; 387: 80–3
  • Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR, et al. Prelingual deafness: high prevalence of a 30delG mutation in the Connexin 26 gene. Hum Mol Genet. 1997; 6: 2173–7
  • Gasparini P, Rabionet R, Barbujani G, Melchionda S, Petersen M, Brondum-Nielsen K, et al. High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG. Eur J Hum Genet. 2000; 8: 19–23
  • Kenneson A, van Naarden Braun K, Boyle C. GJB2 (Connexin 26) variants and non-syndromic sensorineural hearing loss: a HuGE review. Genet Med. 2002; 4: 258–74
  • Lucotte G, Mercier G. Meta-analysis of GJB2 mutation 35delG frequencies in Europe. Genet Test. 2001; 5: 149–52
  • Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, et al. Mutations in the Connexin 26 gene (GJB2) among Ashkenazi Jews with non-syndromic recessive deafness. N Engl J Med. 1998; 339: 1500–5
  • Yan D, Park HJ, Ouyang XM, Pandya A, Doi K, Erdenetungalag R, et al. Evidence of a founder effect for the 235delC mutation of GJB2 (Connexin 26) in east Asians. Hum Genet. 2003; 114: 44–50
  • Loffler J, Nekahm D, Hirst-Stadlmann A, Gunther B, Menzel HJ, Utermann G, et al. Sensorineural hearing loss and the incidence of C×26 mutations in Austria. Eur J Hum Genet. 2001; 9: 226–30
  • Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L, et al. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet. 1998; 351: 394–8
  • del Castillo I, Villamar M, Moreno-Pelayo MA, del Castillo FJ, Alvarez A, Telleria D, et al. A deletion involving the Connexin 30 gene in non-syndromic hearing impairment. N Engl J Med. 2002; 346: 243–9
  • Ahmad S, Chen S, Sun J, Lin X. Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice. Biochem Biophys Res Commun. 2003; 307: 362–8
  • Holt JR, Corey D P. Ion channel defects in hereditary hearing loss. Neuron. 1999; 22: 217–9
  • Marziano NK, Casalotti SO, Portelli AE, Becker DL, Forge A. Mutations in the gene for Connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on Connexin 30. Hum Mol Genet. 2003; 12: 805–12
  • Grifa A, Wagner CA, D'Ambrosio L, Melchionda S, Bernardi F, Lopez-Bigas N, et al. Mutations in GJB6 cause non-syndromic autosomal dominant deafness at DFNA3 locus. Nat Genet. 1999; 23: 16–8
  • Borg E, Canlon B, Engstrom B. Noise-induced hearing loss. Literature review and experiments in rabbits. Morphological and electrophysiological features, exposure parameters and temporal factors, variability and interactions. Scand Audiol Suppl. 1995; 40: 1–147
  • Rabinowitz PM, Pierce Wise J Sr, Hur Mobo B, Antonucci PG, Powell C, Slade M. Antioxidant status and hearing function in noise-exposed workers. Hear Res. 2002; 173: 164–71
  • 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
  • Carlsson PI, Borg E, Grip L, Dahl N, Bondeson M L. Variability in noise susceptibility in a Swedish population: the role of 35delG mutation in the Connexin 26 (GJB2) gene. Audiol Med. 2004; 2: 123–30
  • 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
  • Engel-Yeger B, Zaaroura S, Zlotogora J, Shalev S, Hujeirat Y, Carrasquillo M, et al. The effects of a Connexin 26 mutation – 35delG – on otoacoustic emissions and brainstem evoked potentials: homozygotes and carriers. Hear Res. 2002; 163: 93–100
  • Henderson D, McFadden SL, Liu CC, Hight N, Zheng X Y. The role of antioxidants in protection from impulse noise. Ann N Y Acad Sci. 1999; 884: 368–80
  • Lautermann J, Crann SA, McLaren J, Schacht J. Glutathione-dependent antioxidant systems in the mammalian inner ear: effects of ageing, ototoxic drugs and noise. Hear Res. 1997; 114: 75–82
  • Pryor WA, Prier DG, Church DF. Electron-spin resonance study of mainstream and sidestream cigarette smoke: nature of the free radicals in gas-phase smoke and in cigarette tar. Environ Health Perspect. 1983; 47: 345–55
  • Mukherjee S, Woods L, Weston Z, Williams AB, Das SK. The effect of mainstream and sidestream cigarette smoke exposure on oxygen defence mechanisms of guinea pig erythrocytes. J Biochem Toxicol. 1993; 8: 119–25
  • Diken H, Kelle M, Tumer C, Deniz B, Baylan Y, Sermet A. Effects of cigarette smoking on blood antioxidant status in short-term and long-term smokers. Turk J Med Sci. 2001; 31: 555
  • Toth KM, Berger EM, Beehler CJ, Repine JE. Erythrocytes from cigarette smokers contain more glutathione and catalase and protect endothelial cells from hydrogen peroxide better than erythrocytes from non-smokers. Am Rev Respir Dis. 1986; 134: 281–4
  • Mizoue T, Miyamoto T, Shimizu T. Combined effect of smoking and occupational exposure to noise on hearing loss in steel factory workers. Occup Environ Med. 2003; 60: 56–9
  • Starck J, Toppila E, Pyykko I. Smoking as a risk factor in sensorineural hearing loss among workers exposed to occupational noise. Acta Otolaryngol (Stockh) 1999; 119: 302–5
  • Barone JA, Peters JM, Garabrant DH, Bernstein L, Krebsbach R. Smoking as a risk factor in noise induced hearing loss. J Occup Med. 1987; 29: 741–5
  • Eddy LB, Morgan RJ, Carney HC. Hearing loss due to combined effects of noise and sodium salicylate. ISA Trans. 1976; 15: 103–8
  • Sliwinska-Kowalska M, Zamyslowska-Szmytke E, Szymczak W, Kotylo P, Fiszer M, Wesolowski W, et al. Effects of coexposure to noise and mixture of organic solvents on hearing in dockyard workers. J Occup Environ Med. 2004; 46: 30–8
  • Ward WD. Endogenous factors related to susceptibility to damage from noise. Occup Med. 1995; 10: 561–75
  • Pyykkö I, Toppila E, Starck J, Juhola M, Auramo Y. Database for a hearing conservation program. Scand Audiol. 2000; 29: 52–8
  • Johansson M, Arlinger S. The development of noise induced hearing loss in the Swedish County of Ostergotland in the 1980 and 1990s. Noise Health 2001; 3: 15–28
  • International Organization for Standardization. International Standard ISO 1999 Acoustics: Determination of Occupational Noise Exposure and Estimation of Noise-induced Hearing Impairment. Geneva: International Organization for Standardization; 1990.
  • Taylor W, Pearson J, Mair A, Burns W. Study of noise and hearing in jute weaving. J Acoust Soc Am. 1965; 38: 113–20
  • Lin D, Goldstein JA, Mhatre AN, Lustig LR, Pfister M, Lalwani AK. Assessment of denaturing high-performance liquid chromatography (DHPLC) in screening for mutations in Connexin 26 (GJB2). Hum Mutat. 2001; 18: 42–51
  • Pallares-Ruiz N, Blanchet P, Mondain M, Claustres M, Roux AF. A large deletion including most of GJB6 in recessive non-syndromic deafness: a digenic effect?. Eur J Hum Genet. 2002; 10: 72–6
  • Wu BL, Kenna M, Lip V, Irons M, Platt O. Use of a multiplex PCR/sequencing strategy to detect both Connexin 30 (GJB6) 342 kb deletion and Connexin 26 (GJB2) mutations in cases of childhood deafness. Am J Med Genet. 2003; 121: 102–8
  • Roux AF, Pallares-Ruiz N, Vielle A, Faugere V, Templin C, Leprevost D, et al. Molecular epidemiology of DFNB1 deafness in France. BMC Med Genet. 2004; 5: 5
  • Griffith AJ, Chowdhry AA, Kurima K, Hood LJ, Keats B, Berlin CI, et al. Autosomal recessive non-syndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (Connexin 26) genotype M34T/167delT. Am J Hum Genet. 2000; 67: 745–9
  • Houseman MJ, Ellis LA, Pagnamenta A, Di WL, Rickard S, Osborn AH, et al. Genetic analysis of the Connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss. J Med Genet. 2001; 38: 20–5
  • Feldmann D, Denoyelle F, Loundon N, Weil D, Garabedian EN, Couderc R, et al. Clinical evidence of the non-pathogenic nature of the M34T variant in the Connexin 26 gene. Eur J Hum Genet. 2004; 12: 279–84
  • Kelley PM, Abe S, Askew JW, Smith SD, Usami S, Kimberling WJ. Human Connexin 30 (GJB6), a candidate gene for non-syndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12. Genomics 1999; 62: 172–6
  • Wangemann P, Schacht J. Homeostatic mechanisms in the cochlea. The cochlea, P Dallos, AN Popper, RR Fay. Springer, New York 1996

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.