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Research Article

SOD1 gene polymorphisms in sudden sensorineural hearing loss

, , , , , , , , , , , & show all
Pages 465-469 | Received 17 Oct 2015, Accepted 22 Oct 2015, Published online: 16 Feb 2016

References

  • Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, et al. Genetic and acquired prothrombotic risk factors and sudden hearing loss. Laryngoscope 2007;117:547–51.
  • Uchida Y, Sugiura S, Ando F, Shimokata H, Nakashima T. Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss. Laryngoscope 2010;120:791–5.
  • Uchida Y, Sugiura S, Nakashima T, Ando F, Shimokata H. Contribution of 1425G/A polymorphism in protein kinase C-Eta (PRKCH) gene and brain white matter lesions to the risk of sudden sensorineural hearing loss in a Japanese nested case-control study. J Neurogenet 2011;25:82–7.
  • Nishio N, Teranishi M, Uchida Y, Sugiura S, Ando F, Shimokata H, et al. Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes. Gene 2012;499:226–30.
  • Um JY, Jang CH, Kim KY, Kim SJ, Kim NH, Moon PD, et al. Candidate genes of cerebrovascular disease and sudden sensorineural hearing loss. Clin Appl Thromb Hemost 2010;16:559–62.
  • The International HapMap Project. Nature 2003;426:789–96.
  • El Barbary A, Altschuler RA, Schacht J. Glutathione S-transferases in the organ of Corti of the rat: enzymatic activity, subunit composition and immunohistochemical localization. Hear Res 1993;71:80–90.
  • Cadoni G, Boccia S, Scipione S, Arzani D, Cianfagna F, Ricciardi G, et al. Glutathione s-transferase gene polymorphisms in Italian patients with sudden sensorineural hearing loss. Otol Neurotol 2006;27:1166–9.
  • Spitaler M, Cantrell DA. Protein kinase C and beyond. Nat Immunol 2004;5:785–90.
  • Kubo M, Hata J, Ninomiya T, Matsuda K, Yonemoto K, Nakano T, et al. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. Nat Genet 2007;39:212–17.
  • Pierson MG, Gray BH. Superoxide dismutase activity in the cochlea. Hear Res 1982;6:141–51.
  • Yao X, Rarey KE. Detection and regulation of Cu/Zn-SOD and Mn-SOD in rat cochlear tissues. Hear Res 1996;96:199–203.
  • 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.
  • Liu YM, Li XD, Guo X Liu B, Lin AH Rao SQ. Association between polymorphisms in SOD1 and noise-induced hearing loss in Chinese workers. Acta Otolaryngol. 2010;130:477–86.
  • Carlsson PI, Van Laer L, Borg E, Bondeson ML, Thys M, Fransen E, Van Camp G. The influence of genetic variation in oxidative stress genes on human noise susceptibility. Hear Res 2005;202:87–96.
  • 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;50:2012–18.
  • Teranishi M, Uchida Y, Nishio N, Kato K, Otaka H, Yoshida T, et al. Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière’s disease in a Japanese population. DNA Cell Biol 2012;31:1555–62.
  • Nam SI, Yu GI, Kim HJ, Park KO, Chung JH, Ha E, Shin DH. A polymorphism at -1607 2G in the matrix metalloproteinase-1 (MMP-1) increased risk of sudden deafness in Korean population but not at -519A/G in MMP-1. Laryngoscope 2011;121:171–5.
  • Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995;10:111–13.
  • Welch GN, Loscalzo J. Homocysteine and atherothrombosis. N Engl J Med 1998;338:1042–50.

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