Evidence map›Paper›PMID 41332812›Full record

ArticlemedRxiv : the preprint server for health sciences2025

The Search for a Diagnostic Indicator of Cochlear Deafferentation: Predicting Age and Veteran Status from Auditory Evoked Potential Measures.

Brad N Buran, Morgan Thienpont, Sean D Kampel, Anne E Heassler, Nicole K Whittle, Haley A Szabo, Sarah Verhulst, Naomi F Bramhall

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Brad N BuranOregon Hearing Research Center (OHRC), Oregon Health & Science University, Portland, OR.ORCID 0000-0002-9864-7798
Morgan ThienpontHearing Technology @ WAVES, Department of Information Technology, Ghent University, Belgium.
Sean D KampelVA Rehabilitation Research & Development (RR&D) National Center for Rehabilitative Auditory Research (NCRAR), VA Portland Health Care System, Portland, OR.
Anne E HeasslerVA Rehabilitation Research & Development (RR&D) National Center for Rehabilitative Auditory Research (NCRAR), VA Portland Health Care System, Portland, OR.
Nicole K WhittleVA Rehabilitation Research & Development (RR&D) National Center for Rehabilitative Auditory Research (NCRAR), VA Portland Health Care System, Portland, OR.
Haley A SzaboVA Rehabilitation Research & Development (RR&D) National Center for Rehabilitative Auditory Research (NCRAR), VA Portland Health Care System, Portland, OR.
Sarah VerhulstHearing Technology @ WAVES, Department of Information Technology, Ghent University, Belgium.ORCID 0000-0002-6498-7719
Naomi F BramhallVA Rehabilitation Research & Development (RR&D) National Center for Rehabilitative Auditory Research (NCRAR), VA Portland Health Care System, Portland, OR.ORCID 0000-0003-1660-5322

Funding

Mouse, Man, and Machine: Combining Model Systems to Develop a Biomarker for Cochlear Deafferentation in Humans (Administrative Supplement)R01DC020423 · NIDCD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Naomi Bramhall · 2022 to 2026
$3.3M
NIDCD NIH HHS R01 DC020423RRD VA I50 RX002361
6 · The paper itself

Abstract

Objectives: Cochlear synaptopathy, a type of cochlear deafferentation that occurs with aging and following loud noise exposure, is expected to be common in humans and to have negative impacts on auditory perception. However, there is currently no means for diagnosing cochlear deafferentation in living humans. Auditory brainstem response (ABR) wave I amplitude and the envelope following response (EFR) are auditory evoked potentials that have been proposed as potential non-invasive indicators of cochlear deafferentation. However, these measures may be impacted by outer hair cell (OHC) dysfunction, making them difficult to interpret. One potential method for estimating the degree of deafferentation in individual patients is to combine evoked potential and distortion product otoacoustic emission (DPOAE) measurements with a computational model of the auditory periphery (CMAP). The goal of this study was to evaluate the ability of auditory evoked potentials, with and without the CMAP, to predict risk factors for cochlear synaptopathy (age and history of military noise exposure). Design: In a population of military Veterans and non-Veterans with up to a mild sensorineural hearing loss, a CMAP was used with Bayesian regression to predict synapse numbers across cochlear frequency (synaptograms) for individual human participants based on their ABR, EFR, and/or DPOAE measurements. Linear regression models were then used to evaluate the ability of the synaptograms and various ABR wave I amplitude, EFR magnitude, and DPOAE measurements to predict age and Veteran status. All Veterans were assumed to have at least some history of military noise exposure. Results: High frequency (4 and 5.6 kHz) ABR wave I amplitude measurements and synaptograms generated from high frequency ABR wave I amplitudes performed the best at predicting participant age. Accounting for OHC function (as indicated by DPOAEs) in the generation of the synaptograms or by including DPOAEs in the linear regression models had limited impact on the ability of ABR wave I amplitudes to predict age. DPOAEs were highly predictive of Veteran status, making it difficult to isolate the ability of the auditory evoked potentials to predict Veteran status. Conclusions: High frequency ABR wave I amplitudes and synaptograms generated from high frequency ABR wave I amplitudes were able to predict participant age within approximately 6 years, with or without incorporating DPOAE measurements. This suggests that high frequency ABR wave I amplitude measurements are good candidates for non-invasive diagnosis of age-related cochlear deafferentation and it may not be necessary to use the CMAP or measure DPOAEs to predict deafferentation in individual patients. Unfortunately, specific recommendations for predicting noise-induced cochlear deafferentation could not be ascertained from this study due to confounding related to OHC dysfunction.

Identifiers

PMID41332812
PMCPMC12668096

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.