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Original Article

Auditory event-related potentials and function of the medial olivocochlear efferent system in children with auditory processing disorders

, , , , &
Pages 213-223 | Received 19 Apr 2018, Accepted 14 Nov 2018, Published online: 25 Jan 2019
 

Abstract

Objective: The objectives were to investigate the function of central auditory pathways and of the medial efferent olivocochlear system (MOCS).

Design: Event-related potentials (ERP) were recorded following the delivery of the stimulus /da/ in quiet and in ipsilateral, contralateral, and binaural noise conditions and correlated to the results of the auditory processing disorders (APD) diagnostic test battery. MOCS function was investigated by adding ipsilateral, contralateral, and binaural noise to transient evoked otoacoustic emission recordings. Auditory brainstem responses and pure tone audiogram were also evaluated.

Study Sample: Nineteen children (7 to 12 years old) with APD were compared with 24 age-matched controls.

Results: Otoacoustic emissions and ABR characteristics did not differ between groups, whereas ERP latencies were significantly longer and of higher amplitudes in APD children than in controls, in both quiet and noise conditions. The MOCS suppression was higher in APD children.

Conclusions: Findings indicate that children with APD present with neural deficiencies in both challenging and nonchallenging environments with an increase in the timing of several central auditory processes correlated to their behavioural performances. Meanwhile, their modulation of the auditory periphery under noisy conditions differs from control children with higher suppression.

Acknowledgments

The authors thank all the children and their families for participating in this study, and the Audiology Clinic at Nemours/Alfred I. duPont Hospital for Children and Jobayer Hossain and Li Xie for statistical consultation.

Disclosure statement

No potential conflict of interest was reported by the authors.

This work was supported by NIH 8P20GM103464 (to T.M.).

Additional information

Funding

This work was supported by NIH 8P20GM103464 (to T.M.).

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