References
- Lee KY. Pathophysiology of age-related hearing loss (peripheral and central). Korean J Audiol. 2013;17:45–49.
- Parham K, Lin FR, Coelho DH, et al. Comprehensive management of presbycusis: central and peripheral. Otolaryngol Head Neck Surg. 2013;148:537–539.
- Lin FR, Metter EJ, O’Brien RJ, et al. Hearing loss and incident dementia. Arch Neurol. 2011;68:214–220.
- Hoffman HJ, Dobie RA, Losonczy KG, et al. Declining prevalence of hearing loss in US adults aged 20 to 69 years. JAMA Otolaryngol Head Neck Surg. 2017;143:274–285.
- Sha SH, Taylor R, Forge A, et al. Differential vulnerability of basal and apical hair cells is based on intrinsic susceptibility to free radicals. Hear Res. 2001;155:1–8.
- Sakamoto M, Kaga K, Kamio T. Extended high-frequency ototoxicity induced by the first administration of cisplatin. Otolaryngol Head Neck Surg. 2000;122:828–833.
- Fausti SA, Henry JA, Schaffer HI, et al. High-frequency monitoring for early detection of cisplatin ototoxicity. Arch Otolaryngol Head Neck Surg. 1993;119:661–666.
- Al-Malky G, Dawson SJ, Sirimanna T, et al. High-frequency audiometry reveals high prevalence of aminoglycoside ototoxicity in children with cystic fibrosis. J Cyst Fibros. 2015;14:248–254.
- Matthews LJ, Lee FS, Mills JH, et al. Extended high-frequency thresholds in older adults. J Speech Lang Hear Res. 1997;40:208–214.
- Kumar P, Upadhyay P, Kumar A, et al. Extended high frequency audiometry in users of personal listening devices. Am J Otolaryngol. 2017;38:163–167.
- Han C, Ding D, Lopez MC, et al. Effects of long-term exercise on age-related hearing loss in mice. J Neurosci. 2016;36:11308–11319.
- Ralli M, Troiani D, Podda MV, et al. The effect of the NMDA channel blocker memantine on salicylate-induced tinnitus in rats. Acta Otorhinolaryngol Ital. 2014;34:198–204.
- Shekhawat GS, Searchfield GD, Stinear CM. The relationship between tinnitus pitch and hearing sensitivity. Eur Arch Otorhinolaryngol. 2014;271:41–48.
- Sereda M, Hall DA, Bosnyak DJ, et al. Re-examining the relationship between audiometric profile and tinnitus pitch. Int J Audiol. 2011;50:303–312.
- Pan T, Tyler RS, Ji H, et al. The relationship between tinnitus pitch and the audiogram. Int J Audiol. 2009;48:277–294.
- Ralli M, Greco A, Turchetta R, et al. Somatosensory tinnitus: current evidence and future perspectives. J Int Med Res. 2017;45:933–947.
- Ralli M, Altissimi G, Turchetta R, et al. Somatosensory tinnitus: correlation between cranio-cervico-mandibular disorder history and somatic modulation. Audiol Neurotol. 2016;21:372–382.
- Forge A, Schacht J. Aminoglycoside antibiotics. Audiol Neurootol. 2000;5:3–22.
- Spongr VP, Flood DG, Frisina RD, et al. Quantitative measures of hair cell loss in CBA and C57BL/6 mice throughout their life spans. J Acoust Soc Am. 1997;101:3546–3553.
- Chen GD, Decker B, Krishnan Muthaiah VP, et al. Prolonged noise exposure-induced auditory threshold shifts in rats. Hear Res. 2014;317:1–8.
- Dallos P, Harris D, Ozdamar O, et al. Behavioral, compound action potential, and single unit thresholds: relationship in normal and abnormal ears. J Acoust Soc Am. 1978;64:151–157.
- Takeno S, Harrison RV, Ibrahim D, et al. Cochlear function after selective inner hair cell degeneration induced by carboplatin. Hear Res. 1994;75:93–102.
- Salvi R, Sun W, Ding D, et al. Inner hair cell loss disrupts hearing and cochlear function leading to sensory deprivation and enhanced central auditory gain. Front Neurosci. 2016;10:621.
- Hofstetter P, Ding D, Salvi R. Magnitude and pattern of inner and outer hair cell loss in chinchilla as a function of carboplatin dose. Audiology. 1997;36:301–311.
- Lobarinas E, Salvi R, Ding D. Insensitivity of the audiogram to carboplatin-induced inner hair cell loss in chinchillas. Hear Res. 2013;302:113–120.
- Liberman MC, Kujawa SG. Cochlear synaptopathy in acquired sensorineural hearing loss: manifestations and mechanisms. Hear Res. 2017;349:138–147.
- Fernandez KA, Jeffers PW, Lall K, et al. Aging after noise exposure: acceleration of cochlear synaptopathy in “recovered” ears. J Neurosci. 2015;35:7509–7520.
- Sergeyenko Y, Lall K, Liberman MC, et al. Age-related cochlear synaptopathy: an early-onset contributor to auditory functional decline. J Neurosci. 2013;33:13686–13694.
- Kujawa SG, Liberman MC. Acceleration of age-related hearing loss by early noise exposure: evidence of a misspent youth. J Neurosci. 2006;26:2115–2123.
- Kujawa SG, Liberman MC. Adding insult to injury: cochlear nerve degeneration after “temporary” noise-induced hearing loss. J Neurosci. 2009;29:14077–14085.
- Lobarinas E, Salvi R, Ding D. Selective inner hair cell dysfunction in chinchillas impairs hearing-in-noise in the absence of outer hair cell loss. J Assoc Res Otolaryngol. 2016;17:89–101.
- Huyghe JR, Van Laer L, Hendrickx JJ, et al. Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. Am J Hum Genet. 2008;83:401–407.
- Gopinath B, Flood VM, McMahon CM, et al. Dietary antioxidant intake is associated with the prevalence but not incidence of age-related hearing loss. J Nutr Health Aging. 2011;15:896–900.
- Vaughan N, James K, McDermott D, et al. A 5-year prospective study of diabetes and hearing loss in a veteran population. Otol Neurotol. 2006;27:37–43.
- Van Eyken E, Van Camp G, Van Laer L. The complexity of age-related hearing impairment: contributing environmental and genetic factors. Audiol Neurotol. 2007;12:345–358.
- Viljanen A, Era P, Kaprio J, et al. Genetic and environmental influences on hearing in older women. J Gerontol A Biol Sci Med Sci. 2007;62:447–452.
- Gates GA, Couropmitree NN, Myers RH. Genetic associations in age-related hearing thresholds. Arch Otolaryngol Head Neck Surg. 1999;125:654–659.
- Zheng QY, Johnson KR, Erway LC. Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses. Hear Res. 1999;130:94–107.
- Zheng QY, Johnson KR, Erway LC. Screening mice at the Jackson laboratory for hereditary hearing impairment. Abstract Assoc Res Otolaryngol. 1997;882:221.
- Willott JF, Erway LC, Archer JR, et al. Genetics of age-related hearing loss in mice. II. Strain differences and effects of caloric restriction on cochlear pathology and evoked response thresholds. Hear Res. 1995;88:143–155.
- Johnson KR, Yu H, Ding D, et al. Separate and combined effects of Sod1 and Cdh23 mutations on age-related hearing loss and cochlear pathology in C57BL/6J mice. Hear Res. 2010;268:85–92.
- Kane KL, Longo-Guess CM, Gagnon LH, et al. Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice. Hear Res. 2012;283:80–88.
- McFadden SL, Ding D, Burkard RF, et al. Cu/Zn SOD deficiency potentiates hearing loss and cochlear pathology in aged 129,CD-1 mice. J Comp Neurol. 1999;413:101–112.
- Ohlemiller KK, McFadden SL, Ding DL, et al. Targeted mutation of the gene for cellular glutathione peroxidase (Gpx1) increases noise-induced hearing loss in mice. J Assoc Res Otolaryngol. 2000;1:243–254.
- Li HS, Borg E. Age-related loss of auditory sensitivity in two mouse genotypes. Acta Otolaryngol. 1991;111:827–834.
- Hunter KP, Willott JF. Aging and the auditory brainstem response in mice with severe or minimal presbycusis. Hear Res. 1987;30:207–218.
- Wang Y, Liberman MC. Restraint stress and protection from acoustic injury in mice. Hear Res. 2002;165:96–102.
- Williamson TT, Zhu X, Walton JP, et al. Auditory brainstem gap responses start to decline in mice in middle age: a novel physiological biomarker for age-related hearing loss. Cell Tissue Res. 2015;361:359–369.
- Lowe AS, Walton JP. Alterations in peripheral and central components of the auditory brainstem response: a neural assay of tinnitus. PLoS One. 2015;10:e0117228.
- McFadden SL, Ding D, Salvi R. Anatomical, metabolic and genetic aspects of age-related hearing loss in mice. Audiology. 2001;40:313–321.
- Ding DL, McFadden SL, Wang J, et al. Age- and strain-related differences in dehydrogenase activity and glycogen levels in CBA and C57 mouse cochleas. Audiol Neurootol. 1999;4:55–63.
- Someya S, Xu J, Kondo K, et al. Age-related hearing loss in C57BL/6J mice is mediated by Bak-dependent mitochondrial apoptosis. Proc Natl Acad Sci USA. 2009;106:19432–19437.
- Noben-Trauth K, Zheng QY, Johnson KR. Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet. 2003;35:21–23.
- Mianne J, Chessum L, Kumar S, et al. Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology-directed repair. Genome Med. 2016;8:16.
- Johnson KR, Tian C, Gagnon LH, et al. Effects of Cdh23 single nucleotide substitutions on age-related hearing loss in C57BL/6 and 129S1/Sv mice and comparisons with congenic strains. Sci Rep. 2017;7:44450.
- Buffenstein R, Edrey YH, Yang T, et al. The oxidative stress theory of aging: embattled or invincible? Insights from non-traditional model organisms. Age (Dordr). 2008;30:99–109.
- Perez VI, Bokov A, Van Remmen H, et al. Is the oxidative stress theory of aging dead? Biochim Biophys Acta. 2009;1790:1005–1014.
- Bared A, Ouyang X, Angeli S, et al. Antioxidant enzymes, presbycusis, and ethnic variability. Otolaryngol Head Neck Surg. 2010;143:263–268.
- Unal M, Tamer L, Dogruer ZN, et al. N-acetyltransferase 2 gene polymorphism and presbycusis. Laryngoscope. 2005;115:2238–2241.
- Ates NA, Unal M, Tamer L, et al. Glutathione S-transferase gene polymorphisms in presbycusis. Otol Neurotol. 2005;26:392–397.
- Tsuji T, Yamada K, Kunieda T. Characterization of the dwg mutations: dwg and dwg (Bayer) are new mutant alleles of the Ggt1 gene. Mamm Genome. 2009;20:711–719.
- Ding D, Jiang H, Chen GD, et al. N-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in γ-glutamyl transferase 1 deficient mice. Aging. 2016;8:730–750.
- Pena-Llopis S, Ferrando MD, Pena JB. Fish tolerance to organophosphate-induced oxidative stress is dependent on the glutathione metabolism and enhanced by N-acetylcysteine. Aquat Toxicol. 2003;65:337–360.
- Fetoni AR, Ralli M, Sergi B, et al. Protective effects of N-acetylcysteine on noise-induced hearing loss in guinea pigs. Acta Otorhinolaryngol Ital. 2009;29:70–75.
- James SJ, Slikker W, Melnyk S, et al. Thimerosal neurotoxicity is associated with glutathione depletion: protection with glutathione precursors. Neurotoxicology. 2005;26:1–8.
- Wu HP, Hsu CJ, Cheng TJ, et al. N-acetylcysteine attenuates noise-induced permanent hearing loss in diabetic rats. Hear Res. 2010;267:71–77.
- Ohinata Y, Yamasoba T, Schacht J, et al. Glutathione limits noise-induced hearing loss. Hear Res. 2000;146:28–34.