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Cochlear origin of hearing loss in MELAS syndrome

Sue, CM; Crimmins, DS; Presgrave, CM; Morris, JGL; Lipsett, LJ; Gibson, WPR; ... Byrne, E; + view all (1998) Cochlear origin of hearing loss in MELAS syndrome. Annals of Neurology , 43 (3) 350 - 359. 10.1002/ana.410430313.

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Abstract

There have been few studies investigating the mechanism and nature of the hearing loss that occurs in the mitochondrial disorders. We studied 18 patients with the MELAS A3243G point mutation from four different kindreds. Pure tone audiometry, speech discrimination testing, acoustic reflexes, tympanometry, and brain stem auditory evoked responses were performed to localize the site of pathology in the auditory pathways. In 12 patients, we performed electrocochleography and otoacoustic emissions to assess cochlear involvement. Neuroimaging and promontory nerve stimulation were performed to exclude retrocochlear pathology. Audiological testing confirmed sensorineural hearing loss in 14 of the 18 patients studied; hearing loss was usually gradual in onset, was symmetrical, and initially affected the higher frequencies. In some patients, there were features that distinguished the hearing loss from presbyacusis, including a young age at onset, asymmetrical involvement, stepwise progression, and partial recovery. We treated one patient who had profound bilateral hearing loss with cochlear implantation; this restored good functional hearing. Hearing loss in MELAS syndrome appears to be due to dysfunction of the cochlea, probably resulting from metabolic failure of the stria vascularis and outer hair cells. Cochlear implantation is a therapeutic option worth considering in those patients who become deaf.

Type:Article
Title:Cochlear origin of hearing loss in MELAS syndrome
DOI:10.1002/ana.410430313
UCL classification:UCL > School of Life and Medical Sciences > Faculty of Medical Sciences

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