Literature DB >> 17804975

Auditory efferent function is affected in multiple sclerosis.

Albert Coelho1, Borka Ceranić, Deepak Prasher, David H Miller, Linda M Luxon.   

Abstract

OBJECTIVE: This study evaluated efferent medial olivocochlear (MOC) function in patients with multiple sclerosis (MS). Various afferent auditory abnormalities have been described in MS, but there is a paucity of data on efferent function. The brain stem is a site of predilection for MS plaques and the efferent MOC pathway may be affected at this level.
METHODS: The study included 30 patients who had normal hearing. According to MRI findings, they were divided into two groups: those with an identifiable brain stem lesion (n = 10) and those with MS lesions in other parts of the central nervous system but without demonstrable MS plaques in the brain stem (n = 20). MOC function was evaluated by the olivocochlear suppression test, using transient evoked otoacoustic emissions. All subjects underwent standard auditory tests, including pure-tone audiometry and recording of auditory brain stem evoked responses. Twenty-two healthy subjects with normal hearing, matched for age and gender, served as a reference group for the auditory data.
RESULTS: The results showed that 66.6% of all patients had reduced MOC function, particularly those (90%) with identified lesions of the brain stem on MRI. Furthermore, abnormal MOC function was found in 55% patients without evidence of a brain stem lesion on MRI.
CONCLUSIONS: This study provides the evidence for a deficit of efferent auditory function in the majority of patients with MS. Taking into consideration the possible roles of the MOC system in processing of auditory information, abnormal MOC suppression in patients with MS may explain a variety of auditory presentations that are currently largely overlooked. This study also highlights the diagnostic value of the MOC suppression test as a site-of-lesion diagnostic test in MS and in identifying subtle brain stem lesions undetected by MRI, suggesting that subtle brain stem lesions may exist and that the MOC suppression test is sufficiently sensitive to detect them. Accordingly, the MOC suppression test may provide a tool for an early diagnosis of MS.

Entities:  

Mesh:

Year:  2007        PMID: 17804975     DOI: 10.1097/AUD.0b013e31812f716e

Source DB:  PubMed          Journal:  Ear Hear        ISSN: 0196-0202            Impact factor:   3.570


  6 in total

1.  Pure-tone auditory thresholds are not chronically elevated in multiple sclerosis.

Authors:  Richard L Doty; Isabelle Tourbier; Sherrie Davis; Jennifer Rotz; Jennifer L Cuzzocreo; Jonathan Treem; Neil Shephard; Dzung L Pham
Journal:  Behav Neurosci       Date:  2012-02-06       Impact factor: 1.912

2.  The functional anatomy of central auditory processing.

Authors:  Thomas E Cope; David M Baguley; Timothy D Griffiths
Journal:  Pract Neurol       Date:  2015-05-13

3.  Interleukin-1β and interleukin-1 receptor antagonist appear in grey matter additionally to white matter lesions during experimental multiple sclerosis.

Authors:  Marloes Prins; Charlotta Eriksson; Anne Wierinckx; John G J M Bol; Rob Binnekade; Fred J H Tilders; Anne-Marie Van Dam
Journal:  PLoS One       Date:  2013-12-23       Impact factor: 3.240

4.  Sound Lateralization Test Distinguishes Unimpaired MS Patients from Healthy Controls.

Authors:  Joshua H Bacon; Ilya Kister; Tamar E Bacon; Eliana Pasternak; Yael Strauchler; Joseph Herbert
Journal:  Mult Scler Int       Date:  2014-07-15

5.  Effects of multiple sclerosis on the audio-vestibular system: a systematic review.

Authors:  Evrim Gür; Ghada Binkhamis; Karolina Kluk
Journal:  BMJ Open       Date:  2022-08-17       Impact factor: 3.006

6.  Simultaneous auditory agnosia: Systematic description of a new type of auditory segregation deficit following a right hemisphere lesion.

Authors:  Emma Holmes; Nattawan Utoomprurkporn; Chandrashekar Hoskote; Jason D Warren; Doris-Eva Bamiou; Timothy D Griffiths
Journal:  Cortex       Date:  2020-11-26       Impact factor: 4.027

  6 in total

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