Semin Hear 2013; 34(01): 051-064
DOI: 10.1055/s-0032-1333151
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Assistive Devices for Patients with Auditory Neuropathy: Hearing Aid Use

Rosamaria Santarelli
1   Department of Neuroscience, Service of Audiology and Phoniatrics, University of Padova, Padova, Italy
,
Roberta Rossi
1   Department of Neuroscience, Service of Audiology and Phoniatrics, University of Padova, Padova, Italy
,
Edoardo Arslan
1   Department of Neuroscience, Service of Audiology and Phoniatrics, University of Padova, Padova, Italy
› Author Affiliations
Further Information

Publication History

Publication Date:
29 January 2013 (online)

Abstract

Auditory neuropathy (AN) is a hearing disorder characterized by disruption of temporal coding of acoustic signals in the auditory nerve resulting from lesions involving auditory nerve fibers, the inner hair cells, or their synapses with auditory nerve terminals. Disruption of auditory nerve discharge underlies both the absence of auditory brainstem responses (ABRs) and impairment of speech perception. AN may be related to genetic disorders or result from a wide range of other etiologies. It can be identified either as an isolated disorder (isolated AN) or associated with multisystem involvement (non-isolated AN). Effectiveness and choice of assistive devices depend crucially upon etiology, site of lesion, and stage of the disease. Cochlear implants constitute an effective rehabilitative tool able to restore speech perception in many patients with genetic AN, especially those affected by the isolated form of the disorder. Some children with isolated AN have proved to be good hearing aid users, showing satisfactory open-set speech perception abilities in the aided condition. Over 50% of children discharged from neonatal intensive care units showing the electrophysiological profile of AN (absent ABRs, presence of otoacoustic emissions) benefit from hearing aid use, the provision of amplification resulting in remarkable improvement in speech perception. It can be concluded that differences in cochlear implant outcome or hearing aid use in patients with AN are related to the pathophysiological mechanisms underlying alteration of auditory nerve discharge associated with individual etiologies.

 
  • References

  • 1 Starr A, Zeng FG, Michalewski HJ , et al. Perspectives on auditory neuropathy: disorders of inner hair cell, auditory nerve, and their synapse. In: The Senses: A Comprehensive Reference. New York, NY: Academic Press; 2008: 397-412
  • 2 Zeng F-G, Kong Y-Y, Michalewski HJ, Starr A. Perceptual consequences of disrupted auditory nerve activity. J Neurophysiol 2005; 93: 3050-3063
  • 3 Starr A, Picton TW, Sininger Y, Hood LJ, Berlin CI. Auditory neuropathy. Brain 1996; 119: 741-753
  • 4 Starr A, Sininger YS, Pratt H. The varieties of auditory neuropathy. J Basic Clin Physiol Pharmacol 2000; 11: 215-230
  • 5 Santarelli R. Information from cochlear potentials and genetic mutations helps localize the lesion site in auditory neuropathy. Genome Med 2010; 2: 91
  • 6 Johnson JS, Newport EL. Critical period effects on universal properties of language: the status of subjacency in the acquisition of a second language. Cognition 1991; 39: 215-258
  • 7 Butinar D, Starr A, Zidar J, Koutsou P, Christodoulou K. Auditory nerve is affected in one of two different point mutations of the neurofilament light gene. Clin Neurophysiol 2008; 119: 367-375
  • 8 Santarelli R, Starr A, Michalewski HJ, Arslan E. Neural and receptor cochlear potentials obtained by transtympanic electrocochleography in auditory neuropathy. Clin Neurophysiol 2008; 119: 1028-1041
  • 9 Pangrsic T, Lasarow L, Reuter K , et al. Hearing requires otoferlin-dependent efficient replenishment of synaptic vesicles in hair cells. Nat Neurosci 2010; 13: 869-876
  • 10 Roux I, Safieddine S, Nouvian R , et al. Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell 2006; 127: 277-289
  • 11 Santarelli R, Del Castillo I, Rodríguez-Ballesteros M , et al. Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene. J Assoc Res Otolaryngol 2009; 10: 545-556
  • 12 Starr A, Michalewski HJ, Zeng F-G , et al. Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145- > Ser). Brain 2003; 126: 1604-1619
  • 13 Huang T, Santarelli R, Starr A. Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals. Brain Res 2009; 1300: 97-104
  • 14 Williams PA, Morgan JE, Votruba M. Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathy. Brain 2010; 133: 2942-2951
  • 15 Kjer P, Jensen OA, Klinken L. Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy. Acta Ophthalmol (Copenh) 1983; 61: 300-312
  • 16 Alavi MV, Bette S, Schimpf S , et al. A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy. Brain 2007; 130: 1029-1042
  • 17 American Academy of Pediatrics, Joint Committee on Infant Hearing. Year 2007 position statement: Principles and guidelines for early hearing detection and intervention programs. Pediatrics 2007; 120: 898-921
  • 18 Xoinis K, Weirather Y, Mavoori H, Shaha SH, Iwamoto LM. Extremely low birth weight infants are at high risk for auditory neuropathy. J Perinatol 2007; 27: 718-723
  • 19 Kraus N, Ozdamar O, Stein L, Reed N. Absent auditory brain stem response: peripheral hearing loss or brain stem dysfunction?. Laryngoscope 1984; 94: 400-406
  • 20 Arslan E, Turrini M, Lupi G, Genovese E, Orzan E. Hearing threshold assessment with auditory brainstem response (ABR) and ElectroCochleoGraphy (ECochG) in uncooperative children. Scand Audiol Suppl 1997; 46: 32-37
  • 21 Jiang ZD, Brosi DM, Shao XM, Wilkinson AR. Sustained depression of brainstem auditory electrophysiology during the first months in term infants after perinatal asphyxia. Clin Neurophysiol 2008; 119: 1496-1505
  • 22 Jiang ZD, Wu YY, Liu XY, Wilkinson AR. Depressed brainstem auditory function in children with cerebral palsy. J Child Neurol 2011; 26: 272-278
  • 23 Amatuzzi M, Liberman MC, Northrop C. Selective inner hair cell loss in prematurity: a temporal bone study of infants from a neonatal intensive care unit. J Assoc Res Otolaryngol 2011; 12: 595-604
  • 24 Roush P, Frymark T, Venediktov R, Wang B. Audiologic management of auditory neuropathy spectrum disorder in children: a systematic review of the literature. Am J Audiol 2011; 20: 159-170
  • 25 Rance G, Barker EJ. Speech and language outcomes in children with auditory neuropathy/dys-synchrony managed with either cochlear implants or hearing aids. Int J Audiol 2009; 48: 313-320
  • 26 Teagle HFB, Roush PA, Woodard JS , et al. Cochlear implantation in children with auditory neuropathy spectrum disorder. Ear Hear 2010; 31: 325-335
  • 27 Rodríguez-Ballesteros M, del Castillo FJ, Martín Y , et al. Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF). Hum Mutat 2003; 22: 451-456
  • 28 Miyamoto RT, Kirk KI, Renshaw J, Hussain D. Cochlear implantation in auditory neuropathy. Laryngoscope 1999; 109: 181-185
  • 29 Brookes JT, Kanis AB, Tan LY, Tranebjaerg L, Vore A, Smith RJ. Cochlear implantation in deafness-dystonia-optic neuronopathy (DDON) syndrome. Int J Pediatr Otorhinolaryngol 2008; 72: 121-126
  • 30 Starr A, Isaacson B, Michalewski HJ , et al. A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells. J Assoc Res Otolaryngol 2004; 5: 411-426
  • 31 Breneman AI, Gifford RH, Dejong MD. Cochlear implantation in children with auditory neuropathy spectrum disorder: long-term outcomes. J Am Acad Audiol 2012; 23: 5-17
  • 32 Rance G, Cone-Wesson B, Wunderlich J, Dowell R. Speech perception and cortical event related potentials in children with auditory neuropathy. Ear Hear 2002; 23: 239-253
  • 33 Lee DS, Lee JS, Oh SH , et al. Cross-modal plasticity and cochlear implants. Nature 2001; 409: 149-150
  • 34 Boothroyd A. The acoustic speech signal. In: Pediatric Audiology: Diagnosis, Technology, and Management. New York, NY: Thieme; 2008: 159-167
  • 35 Varga R, Kelley PM, Keats BJ , et al. Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene. J Med Genet 2003; 40: 45-50
  • 36 Delmaghani S, del Castillo FJ, Michel V , et al. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nat Genet 2006; 38: 770-778
  • 37 Schoen CJ, Emery SB, Thorne MC , et al. Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila. Proc Nat. Acad Sci USA 2010; 107: 13396-13401
  • 38 Wang Q, Li R, Zhao H , et al. Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation. Am J Med Genet A 2005; 133A: 27-30
  • 39 Kovach MJ, Campbell KCM, Herman K , et al. Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: delineation of the clinical features and review of the literature. Am J Med Genet 2002; 108: 295-303
  • 40 Kalaydjieva L, Gresham D, Gooding R , et al. N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom. Am J Hum Genet 2000; 67: 47-58
  • 41 López-Bigas N, Olivé M, Rabionet R , et al. Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment. Hum Mol Genet 2001; 10: 947-952
  • 42 Bähr M, Andres F, Timmerman V, Nelis ME, Van Broeckhoven C, Dichgans J. Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene. J Neurol Neurosurg Psychiatr 1999; 66: 202-206
  • 43 Amati-Bonneau P, Guichet A, Olichon A , et al. OPA1 R445H mutation in optic atrophy associated with sensorineural deafness. Ann Neurol 2005; 58: 958-963
  • 44 Meyer E, Michaelides M, Tee LJ , et al. Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy. Mol Vis 2010; 16: 650-664
  • 45 Rance G, Fava R, Baldock H , et al. Speech perception ability in individuals with Friedreich ataxia. Brain 2008; 131: 2002-2012
  • 46 Wang QJ, Li QZ, Rao SQ , et al. AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23-27.3. J Med Genet 2006; 43: e33
  • 47 Bahmad F, Merchant SN, Nadol JB, Tranebjaerg L. Otopathology in Mohr-Tranebjaerg syndrome. Laryngoscope 2007; 117: 1202-1208
  • 48 Ceranić B, Luxon LM. Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatr 2004; 75: 626-630