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Auditory Brainstem Response Altered in Humans With Noise Exposure Despite Normal Outer Hair Cell Function
Naomi F Bramhall1, Dawn Konrad-Martin, Garnett P McMillan
11VA RR&D National Center for Rehabilitative Auditory Research (NCRAR), VA Portland Health Care System, Portland, Oregon, USA; and 2Department of Otolaryngology/HNS, Oregon Health & Science University, Portland, Oregon, USA.
Higher noise exposure in young adults, even with normal hearing, is linked to reduced auditory brainstem response (ABR) wave I amplitudes, suggesting potential cochlear synaptopathy.
Area of Science:
- Auditory Neuroscience
- Otoacoustic Emissions
- Neurophysiology
Background:
- Cochlear synaptopathy, a loss of synapses between inner hair cells and auditory nerve fibers, can occur after noise exposure without affecting hearing thresholds.
- Animal studies show noise-induced synaptopathy correlates with reduced auditory brainstem response (ABR) wave I amplitude.
Purpose of the Study:
- To investigate the association between lifetime noise exposure history and ABR wave I amplitudes in young adults with normal hearing thresholds.
- To determine if noise exposure impacts auditory nerve function even in the absence of threshold shifts.
Main Methods:
- Twenty-nine young military Veterans and 35 non-Veterans (19-35 years) with normal hearing were grouped by self-reported noise exposure.
- Suprathreshold ABRs and distortion product otoacoustic emissions (DPOAEs) were measured at 1, 3, 4, and 6 kHz.
Main Results:
- Higher self-reported noise exposure histories were associated with significantly smaller ABR wave I amplitudes across all tested frequencies.
- These findings persisted after controlling for sex and outer hair cell function (DPOAEs).
Conclusions:
- Reduced suprathreshold ABR wave I amplitudes in individuals with high noise exposure histories may indicate subclinical cochlear damage, potentially cochlear synaptopathy.
- This damage occurs independently of outer hair cell function and is consistent with animal models, though direct evidence of synaptopathy requires further study.
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