Evidence map›Paper›PMID 38086151›Full record

ArticleHearing research2024

Comprehensive behavioral and physiologic assessment of peripheral and central auditory function in individuals with mild traumatic brain injury.

Amy N Stahl, Jordan M Racca, Cailey I Kerley, Adam Anderson, Bennett Landman, Linda J Hood, René H Gifford, Tonia S Rex

Open access · hybridAbstract read
In one paragraph

Article in Hearing research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Traumatic brain injury impact on normal hearing.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2026
    Review
  2. Article
  3. Article
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 at 2 institutions in 1 country.

Amy N StahlNeuroscience Graduate Program, Vanderbilt University, Nashville, TN USA; Department of Ophthalmology & Visual Sciences, Vanderbilt Eye Institute, Vanderbilt University Medical Center, Nashville, TN USA.
Jordan M RaccaDepartment of Hearing & Speech Sciences, Vanderbilt University Medical Center, Nashville, TN USA; Collaborative for STEM Education and Outreach, Vanderbilt Peabody College of Education, Vanderbilt University, Nashville, TN USA.
Cailey I KerleyDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN, USA.
Adam AndersonDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.
Bennett LandmanDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN, USA.
Linda J HoodDepartment of Hearing & Speech Sciences, Vanderbilt University Medical Center, Nashville, TN USA.
René H GiffordDepartment of Hearing & Speech Sciences, Vanderbilt University Medical Center, Nashville, TN USA.
Tonia S RexDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA. Electronic address: tonia.rex@vumc.org.
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey L Neul · 2020 to 2026
$10.3M
Training in Fundamental NeuroscienceT32MH064913 · NIMH · VANDERBILT UNIVERSITY · PI IHRIE, REBECCA A, WINDER, DANNY G. · 2001 to 2022
$7.6M
Retinal Ganglion Cell Replacement in Clinically Relevant Models of Optic NeuropathyU24EY029893 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BARANOV, PETR, REX, TONIA S · 2018 to 2022
$7.2M
Role of the Nrf2/ARE pathway in retinal ganglion cells during glaucoma pathogenesis and neuroprotectionR01EY022349 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CALKINS, DAVID J., REX, TONIA S · 2012 to 2021
$3.8M
NEI NIH HHS P30 EY008126NEI NIH HHS R01 EY022349NEI NIH HHS U24 EY029893NICHD NIH HHS P50 HD103537NIMH NIH HHS T32 MH064913
6 · The paper itself

Abstract

Auditory complaints are frequently reported by individuals with mild traumatic brain injury (mTBI) yet remain difficult to detect in the absence of clinically significant hearing loss. This highlights a growing need to identify sensitive indices of auditory-related mTBI pathophysiology beyond pure-tone thresholds for improved hearing healthcare diagnosis and treatment. Given the heterogeneity of mTBI etiology and the diverse peripheral and central processes required for normal auditory function, the present study sought to determine the audiologic assessments sensitive to mTBI pathophysiology at the group level using a well-rounded test battery of both peripheral and central auditory system function. This test battery included pure-tone detection thresholds, word understanding in quiet, sentence understanding in noise, distortion product otoacoustic emissions (DPOAEs), middle-ear muscle reflexes (MEMRs), and auditory evoked potentials (AEPs), including auditory brainstem responses (ABRs), middle latency responses (MLRs), and late latency responses (LLRs). Each participant also received magnetic resonance imaging (MRI). Compared to the control group, we found that individuals with mTBI had reduced DPOAE amplitudes that revealed a compound effect of age, elevated MEMR thresholds for an ipsilateral broadband noise elicitor, longer ABR Wave I latencies for click and 4 kHz tone burst elicitors, longer ABR Wave III latencies for 4 kHz tone bursts, larger MLR Na and Nb amplitudes, smaller MLR Pb amplitudes, longer MLR Pa latencies, and smaller LLR N1 amplitudes for older individuals with mTBI. Further, mTBI individuals with combined hearing difficulty and noise sensitivity had a greater number of deficits on thalamic and cortical AEP measures compared to those with only one/no self-reported auditory symptoms. This finding was corroborated with MRI, which revealed significant structural differences in the auditory cortical areas of mTBI participants who reported combined hearing difficulty and noise sensitivity, including an enlargement of left transverse temporal gyrus (TTG) and bilateral planum polare (PP). These findings highlight the need for continued investigations toward identifying individualized audiologic assessments and treatments that are sensitive to mTBI pathophysiology.

Indexed as

Brain ConcussionHearing LossAuditory ThresholdEvoked Potentials, AuditoryEvoked Potentials, Auditory, Brain StemHearingHumansNoiseOtoacoustic Emissions, SpontaneousAuditory brainstem responses (ABRs)Distortion product otoacoustic emissions (DPOAEs)Late latency responses (LLRs)Middle-ear muscle reflexes (MEMRs)Middle latency responses (MLRs)Speech understanding in noise (QuickSIN)Traumatic brain injury (TBI)

Identifiers

PMID38086151
PMCPMC11978228
OpenAlexW4389340690

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.